DNA烷基化损伤修复及其在肿瘤化疗中的意义

DNA alkylation lesion repair: outcomes and implications in cancer chemotherapy DNA烷基化损伤修复及其在肿瘤化疗中的意义 1 2 first-author https://orcid.org/0000-0002-7589-661X 1 2 Huadong PEI, huadongpei@gwu.edu Huadong PEI, huadongpei@gwu.edu huadongpei@gwu.edu Department of Biochemistry and Molecular Medicine, the George Washington University School of Medicine and Health Sciences, Washington, DC 20037, USA Department of Biochemistry and Molecular Medicine, the George Washington University School of Medicine and Health Sciences, Washington, DC 20037, USA GW Cancer Center, the George Washington University School of Medicine and Health Sciences, Washington, DC 20052, USA GW Cancer Center, the George Washington University School of Medicine and Health Sciences, Washington, DC 20052, USA Alkylated DNA lesions, induced by both exogenous chemical agents and endogenous metabolites, represent a major form of DNA damage in cells. The repair of alkylation damage is critical in all cells because such damage is cytotoxic and potentially mutagenic. Alkylation chemotherapy is a major therapeutic modality for many tumors, underscoring the importance of the repair pathways in cancer cells. Several different pathways exist for alkylation repair, including base excision and nucleotide excision repair, direct reversal by methyl-guanine methyltransferase (MGMT), and dealkylation by the AlkB homolog (ALKBH) protein family. However, maintaining a proper balance between these pathways is crucial for the favorable response of an organism to alkylating agents. Here, we summarize the progress in the field of DNA alkylation lesion repair and describe the implications for cancer chemotherapy. DNA烷基化损伤作为细胞内一种主要的DNA损伤形式，可由外源性化学试剂和内源性代谢物诱导发生。DNA烷基化损伤具有细胞毒性并可能诱导突变，因此烷基化损伤修复在所有细胞内都至关重要。同时，烷基化肿瘤化学疗法是许多肿瘤的主要治疗方案，这也强调了癌细胞内烷基化修复途径的重要性。烷基化修复的途径包括碱基切除和核苷酸切除修复、甲基鸟嘌呤甲基转移酶（MGMT）的直接逆转以及ALKBH蛋白家族的脱烷基化作用。然而，这些修复途径之间的内部平衡才是机体有效应答DNA烷基化试剂的关键所在。在这里，我们总结了DNA烷基化损伤修复领域的进展，并进一步描述该领域的研究对肿瘤化疗的深刻意义。 Alkylation repair Base excision repair Methyl-guanine methyltransferase (MGMT) AlkB homolog (ALKBH) DNA烷基化修复 碱基切除修复 甲基鸟嘌呤甲基转移酶（MGMT） ALKBH 1 Introduction 1 The importance of the inevitable DNA base adduct is dictated by the variable biological effects elicited in cells. Even for one single type of DNA base adduct, the biological effects can vary depending on its chemical structure, distribution within the genome, response pathways or repair mechanisms, and other factors. DNA alkylation, upon which a small or more complex alkyl group is added, constitutes one major class of DNA base adduct in the biological system. Because of its undesirable causes and deleterious effects on genome integrity, DNA alkylation is generally considered a type of DNA lesion ( Fu et al., 2012 Fu et al., 2012 ; Soll et al., 2017 Soll et al., 2017 ). To counter alkylated DNA lesion in cells, individual factors are mobilized to recognize each specific adduct, calling for an interplay or competition of multiple highly conserved repair pathways. Consequently, the conversation between these repair pathways could either sequester or further elicit genotoxicity, therefore complicating the biological effects in cells ( Tsuzuki et al., 1998 Tsuzuki et al., 1998 ; Fu et al., 2012 Fu et al., 2012 ; Soll et al., 2017 Soll et al., 2017 ). Meanwhile, researchers are systematically considering alkylating agents that induce alkylation lesions in cells as a promising chemotherapeutic option for cancer treatment. Because of the agents' broad activity, each alkylating agent can induce a spectrum of alkylation lesions in cells, in turn eliciting convergence of different repair pathways and further complicating the biological effects ( Drabløs et al., 2004 Drabløs et al., 2004 ; Fu et al., 2012 Fu et al., 2012 ; Soll et al., 2017 Soll et al., 2017 ). In this review, we focus on the regulation and the outcomes of the DNA alkylation lesion repair, and how these outcomes influence carcinogenesis and individual response to cancer chemotherapy. 2 Complexity in DNA alkylation lesions 1 DNA alkylation lesions generated in the biological system are unavoidable due to the ubiquitously presented alkylating agents and the high nucleophilic character of DNA bases. Each alkylating agent has broad reactivity and may induce numerous alkylation lesions. These lesions vary in terms of their chemical structure and distribution in the genome, leading to variable consequences in cells. 2.1 Alkylating agents 2 Alkylating agents are basically chemical compounds which can reactively transfer alkyl carbon groups onto the high nucleophilic nitrogen or oxygen atoms on DNA bases ( Shrivastav et al., 2010 Shrivastav et al., 2010 ; Fu et al., 2012 Fu et al., 2012 ; Soll et al., 2017 Soll et al., 2017 ). These compounds may arise both endogenously and exogenously. While external sources are well documented, the internal donor of the alkyl group is not clearly defined. It has been suggested that the methyl donor S -adenosylmethionine (SAM), along with several other methyl metabolites, may serve as a potential source ( Barrows and Magee, 1982 Barrows and Magee, 1982 ; Rydberg and Lindahl, 1982 Rydberg and Lindahl, 1982 ). There are five major classes of alkylating agents, differing in the number of reactive sites, the type of alkyl groups transferred, or the particular chemical reactivity ( Table 1 Table 1 ). Usually, a bifunctional alkylating agent contains more than one reactive site, which can react with separate DNA bases to form cross-links or bulky DNA adducts. Conversely, a monofunctional alkylating agent contains only one reactive group, either a simple methyl or a complex alkyl group. All of the alkylating agents attack DNA bases through a nucleophilic substitution reaction (monomolecular nucleophilic substitution (S N 1) or bimolecular nucleophilic substitution 2 (S N 2)). S N 2-type alkylating agents mainly react with the ring nitrogen atoms on the bases, while S N 1-type alkylating agents can react with both nitrogen and excircle oxygen atoms on the bases. Notably, most clinics favor S N 1-type alkylating agents ( Table 1 Table 1 ), whereas S N 2-type alkylating agents may also be beneficial due to their relative selectivity. S N 1: monomolecular nucleophilic substitution; S N 2: bimolecular nucleophilic substitution 2; N 7 meG: N 7 -methylguanine; N 3 meA: N 3 -methyladenine; N 1 meA: N 1 -methyladenine; N 3 meC: N 3 -methylcytosine; O 6 meG: O 6 -methylguanine; O 6 Cl-ethylG: O 6 -chloroethylguanie; N 1 , O 6 -EG: N 1 , O 6 -ethanoguanine. Category Name Mono (M)/Bi (B) functional S N 1/S N 2 DNA lesion Clinical application 2 Alkyl sulfonates Busulfan B S N 2 G-A cross-link G-G cross-link Leukemia, polycythemia vera, myeloid metaplasia Methyl methanesulfonate M S N 2 N 7 meG N 3 meA N 1 meA N 3 meC N/A 4 Triazene Dacarbazine 4 M 4 S N 1 4 N 7 meG N 3 meA O 6 meG Metastatic melanoma, Hodgkin’s lymphoma, sarcoma Procarbazine Malignant glioma, Hodgkin’s lymphoma Temozolomide Malignant glioma Streptozotocin Pancreatic islet cell cancer 4 Nitrosoureas Nimutine 4 M 4 S N 1 4 N 7 -alkylG O 6 Cl-ethylG N 1 , O 6 -EG G-C cross-link G-G cross-link Brain tumors, solid tumors Carmustine Brain tumors, lymphoma, melanoma Lomustine Brain tumors, lymphoma, melanoma Fotemustine Metastatic melanoma 5 Nitrogen mustards Mechlorethamine 5 B 5 S N 1 5 N 7 -alkylG O 6 -alkylG G-G cross-link G-A cross-link 5 Lymphoma, leukemia, multiple myeloma, ovarian cancer, solid tumors Cyclophosphamide Melphalan Bendamustine Chlorambucil 3 Aziridines Altretamine 3 B 3 S N 1 3 N 7 -alkylG O 6 -alkylG G-G cross-link G-A cross-link Recurrent ovarian cancer Mitomycin C Breast cancer, gastrointestinal tumor Thiotepa Breast cancer, ovarian cancer, bladder cancer 2.2 Variety of alkylation lesions induced in cells 2 Depending on the type of alkyl groups and the position of the bases during the reaction, there are a wide variety of alkylation lesions, ranging from large helix distortions to small base adducts ( Table 1 Table 1 ). For example, the chloroethyl group provided by chloroethylating agents such as nitrosourea compounds can react with the N 7 and O 6 positions of guanine to generate chloroethyl adducts. The O 6 chloroethyl guanine may react with the nearby cytosine through a spontaneous chemical rearrangement, generating a guanine-cytosine intrastrand or interstrand cross-link ( Warren et al., 2006 Warren et al., 2006 ). These lesions are highly cytotoxic and require the involvement of the nucleotide excision repair (NER) or the Fanconi anemia (FA) pathway ( Hong et al., 2007 Hong et al., 2007 ; Deans and West, 2011 Deans and West, 2011 ). Methyl DNA adducts, introduced by most clinically used methyl alkylating agents, are the simplest alkylation lesions and cause less distortion in the DNA. Because of the high nucleophilic character, nearly 70% of the total alkylation lesions in cells, induced by either S N 1 or S N 2 monofunctional alkylating agents, are the relatively innocuous N 7 -methylguanine type ( N 7 meG). However, N 7 meG spontaneously depurates to generate an abasic (AP) site, which may cause replication collapse and have a tendency to introduce mutations ( Beranek, 1990 Beranek, 1990 ; Gentil et al., 1992 Gentil et al., 1992 ). The less popular N 3 -methyladenine type ( N 3 meA) (about 10%) causes more replication block but less transcription block, because it usually presents in the minor groove of DNA helices, where most error-free DNA polymerases, but not RNA polymerase II, are loaded ( Morales and Kool, 1999 Morales and Kool, 1999 ; Naryshkin et al., 2000 Naryshkin et al., 2000 ). Meanwhile, translesion polymerases can bypass such lesions, but at the risk of more mutations ( Larson et al., 1985 Larson et al., 1985 ; Johnson et al., 2007 Johnson et al., 2007 ). O -methyl lesions, including O 6 -methylguanine ( O 6 meG) and O 4 -methylthymine ( O 4 meT), are potentially mutagenic because of the readily formed mispairs, which can also be cytotoxic in cells through the subsequent processing of the mismatch repair (MMR) machinery ( Warren et al., 2006 Warren et al., 2006 ). N 1 -methyladenine ( N 1 meA) and N 3 -methylcytosine ( N 3 meC) lesions, minor lesions mainly induced by S N 2 alkylating agents, disrupt the base pair and are intrinsically cytotoxic, but less likely to be mutagenic ( Shrivastav et al., 2010 Shrivastav et al., 2010 ). The diversity of the types of DNA alkylation damage necessitates the involvement of a number of DNA repair systems, which include multi-step base-excision repair (BER), direct reversal by methylguanine methyltransferase (MGMT), and direct demethylation by the AlkB homolog (ALKBH) family proteins ( Fig. 1 Fig. 1 ). These mechanisms collectively modulate the biological effects of alkylation lesions and in turn provide strong instructions for cancer prevention or treatment. 3 BER as the major tool for alkylated DNA lesion 1 In either prokaryotic or eukaryotic system, BER is the primary mechanism for removing small DNA base lesions, including most of the alkylated lesions. BER occurs through two major sub-pathways which differ in the repair gap size: short-patch or long-patch BER. Both sub-pathways share general procedures including the recognition and removal of the damaged nucleotide, gap filling by DNA synthesis, and subsequent ligation into the pre-existing DNA strand ( Fig. 1 Fig. 1 a). The multistep nature of the BER pathway inevitably gives rise to several toxic intermediates (5'-deoxyribose phosphate (5'-dRP), AP site, single-strand break (SSB)), thus necessitating proper coordination between BER pathway players. 3.1 Recognition of alkylated lesions by DNA glycosylase 2 To initiate the BER pathway in cells, a specific DNA glycosylase is usually required to correctly recognize and excise the damaged base. The substrate preference of a glycosylase determines its role in particular repair pathways ( Svilar et al., 2011 Svilar et al., 2011 ). In dealing with alkylated lesions, the predominant glycosylase in higher eukaryotic cells is the alkyladenine-DNA glycosylase (AAG; also known as N -methylpurine DNA glycosylase (MPG)). AAG exclusively catalyzes the hydrolysis of the N -glycosidic bond between the alkylated base and the ribose, thereby generating an AP site for subsequent repair. Both in vitro assays and genetic studies have confirmed that most of the alkylated purines (e.g., N 7 meG, N 3 meA) are preferentially repaired by AAG ( Lindahl, 1993 Lindahl, 1993 ; Jacobs and Schär, 2012 Jacobs and Schär, 2012 ). However, Aag -/- mice exhibited neither significant development defects nor severe spontaneous mutation rates ( Engelward et al., 1997 Engelward et al., 1997 ), indicating that these alkylated lesions induced by endogenous alkylating agents can be tolerated by other back-up repair mechanisms (such as translesion synthesis (TLS) or MMR). Conversely, it is believed that the excessive activity of AAG may introduce more AP sites in cells, which are more detrimental. Importantly, compared to normal littermates, Aag -/- mice are more prone to develop colon cancer induced by azoxymethane-dextran sodium sulfate (AOM-DSS) ( Meira et al., 2008 Meira et al., 2008 ). This suggests that AAG mainly protects against mutagenicity rather than the cytotoxicity elicited by overwhelming alkylation lesions. While AAG spontaneously and effectively searches its substrate in the native DNA context, substrate searching in the chromatin is extremely inefficient (about 80% reduction), as revealed by in vitro assay ( Olmon and Delaney, 2017 Olmon and Delaney, 2017 ). This raises the question of how AAG effectively recognizes the alkylated purines in cells. There are two major models recently proposed. (1) Recruitment of AAG on lesions by transcription or replication machinery, as supported by a relative predisposition of BER to occur on the active transcribing or replicating regions ( Odell et al., 2013 Odell et al., 2013 ; Bjørås et al., 2017 Bjørås et al., 2017 ). Biochemical studies showed that AAG interacts with both transcription repressors (e.g., methyl-CpG-binding domain protein 1 (MBD1)) and elongators (e.g., elongator complex protein 1 (ELP1)) ( Watanabe et al., 2003 Watanabe et al., 2003 ; Huttlin et al., 2017 Huttlin et al., 2017 ; Montaldo et al., 2019 Montaldo et al., 2019 ). These interactions enhance the AAG-mediated repair along transcription units and may also contribute to localized gene expression ( Montaldo et al., 2019 Montaldo et al., 2019 ). However, a thoroughly developed genome-wide profiling approach is needed to dissect the distribution of AAG and its associated chaperons in the genome. (2) Reorganization of the chromatin structure to favor the repair, as supported by the different chromatin structures observed before and after BER ( Odell et al., 2013 Odell et al., 2013 ). Importantly, these favorable chromatin structures are documented to be pivotal for most of the downstream factors in BER, including AP endonuclease 1 (APE1), X-ray repair cross-complementing group 1 (XRCC1), and polymerase β (Pol β) ( Odell et al., 2011 Odell et al., 2011 ; Rodriguez and Smerdon, 2013 Rodriguez and Smerdon, 2013 ; Rodriguez et al., 2017 Rodriguez et al., 2017 ). However, firm evidence demonstrating that AAG associates with any chromatin structures or histone marks is lacking. In any case, the difference in the BER factor loading demonstrates an inequality of repair across the genome. Whether this inequality in cells contributes to tissue or organ specificity is another interesting question which may widen our understanding of the biological effects of alkylation lesions. 3.2 Deleterious consequences of BER imbalance 2 After initiation by DNA glycosylases, imbalance in each step of BER may cause accumulation of toxic intermediates and have a profound biological effect ( Fig. 2 Fig. 2 a). These intermediates include the genotoxic AP site, 5'-dRP or 3'-hydroxyl (3'-OH), and SSB (as generated sequentially by AAG, APE1, and Pol β) ( Fig. 1 Fig. 1 a). Unlike the original alkylated lesions, these unrepaired intermediates can consequently collapse to double-strand breaks (DSBs), which may introduce more severe deleterious effects due to excessive activity of homologous recombination (HR) ( Sossou et al., 2005 Sossou et al., 2005 ; Ströbel et al., 2017 Ströbel et al., 2017 ; Yuan et al., 2017 Yuan et al., 2017 ). Indeed, excessive activity of AAG or loss of the APE1 in cells causes higher microsatellite instability, spontaneous frameshift mutagenesis, and chromatin aberrations ( Coquerelle et al., 1995 Coquerelle et al., 1995 ; Hofseth et al., 2003 Hofseth et al., 2003 ; Klapacz et al., 2010 Klapacz et al., 2010 ). Another key BER protein, XRCC1, acts as a scaffold to coordinate the DNA excision and ligation by interacting with both DNA Pol β and ligase III (LIG III) ( Fig. 1 Fig. 1 a). Hence, cells deficient in XRCC1 display accumulated SSB and severe hypersensitivity to alkylating agents ( Fan et al., 2007 Fan et al., 2007 ; Hoch et al., 2017 Hoch et al., 2017 ). Moreover, polymorphisms in XRCC1 are found to correlate with the development of several solid tumors (Jiang et al., 2009). Similarly, alterations in Polβ are observed in almost 30% of human cancers ( Starcevic et al., 2004 Starcevic et al., 2004 ). Apart from DNA polymerase activity, Pol β also excises the 5'-dRP moiety ( Feng et al., 1998 Feng et al., 1998 ). Mutagenesis study has demonstrated that missense mutations which disrupt the excision activity of Pol β confer hypersensitivity to alkylating agents ( Sobol et al., 2000 Sobol et al., 2000 ), suggesting high cytotoxicity of the 5'-dRP moiety. Collectively, the imbalance of BER conferred by abnormal alteration of BER players poses a huge threat to genome integrity; it can significantly influence carcinogenesis and alkylation chemotherapy response. 3.3 Competing mechanisms for processing inter-mediates 2 The presentation of intermediates in the BER pathway may also engage the convergence and competition of the BER sub-pathways. Though it remains unclear how the sub-pathway transition occurs, it is certain that the initiation by the specific glycosylase, the size of the repaired gap, and the cell cycle are all critical. At the molecular level, the processing of the 5'-dRP moiety may well be the turning point ( Fig. 1 Fig. 1 a). In short-patch BER, the 5'-dRP moiety is removed by Pol β and subsequently filled, with the XRCC1 working as a scaffold. In long-patch BER, these gaps are branched by proliferating cell nuclear antigen (PCNA); therefore, the replicative DNA polymerase δ/ε (Pol δ/ε) can fill the gap. Thus, long-patch BER may largely associates with the replication machinery and mainly occurs during replication. However, it is not clear whether long-patch BER can also occur in non-proliferating cells. One model to explain the molecular mechanism concerning the sub-pathway choice suggests that high-mobility group box 1 (HMGB1) acts as an important director toward long-patch BER. Mechanistically, HMGB1 can block the 5'-dRP moiety from Pol β and at the same time interact with enzymes which play a role in the long-patch BER pathway ( Prasad et al., 2007 Prasad et al., 2007 ; Liu et al., 2010 Liu et al., 2010 ). However, it is unclear whether HMGB1 acts exclusively as the sole switcher, as it also functions in multiple DNA repair pathways. In addition, 5'-dRP lesions could be initially processed by Pol β and then subject to Pol δ/ε, either in a PCNA-dependent or -independent manner ( Asagoshi et al., 2010 Asagoshi et al., 2010 ). Nevertheless, these two sub-pathways occur simultaneously in most cells, with long-patch BER exhibiting higher efficiency in repairing longer gaps than short-patch BER. Another competition may occur in the processing of AP sites generated by AAG. Recent studies showed that loss of a novel AP site sensor 5-hydroxymethylcytosine (5hmC) binding, ES cell-specific (HMCES) in cells causes accumulation of AP sites, either spontaneously or in response to methyl-methane sulfonate (MMS), suggesting a role for HMCES in relieving the cytotoxicity of AP sites ( Mohni et al., 2019 Mohni et al., 2019 ; Mehta et al., 2020 Mehta et al., 2020 ). In vitro assay indicates that HMCES covalently attaches to AP sites in single-stranded DNA (ssDNA) to form a DNA protein complex (DPC), which protects genome stability in S phase ( Mohni et al., 2019 Mohni et al., 2019 ). Interestingly, lack of HMCES not only sensitizes cells to alkylating agents, but also induces higher mutagenicity, suggesting that factors in these mechanisms may compete with each other ( Fig. 2 Fig. 2 b) ( Mohni et al., 2019 Mohni et al., 2019 ). Unfortunately, the detailed repair mechanism of HMCES-mediated repair is not well defined. The clinical relevance of HMCES and alkylating chemotherapy drug response needs further investigation. 3.4 BER pathway and implications for cancer chemotherapy 2 BER players have been documented as important modulators in cancer chemotherapy. For example, APE1 endonuclease activity on AP sites contributes to the alkylating agent resistance in medulloblastomas and neuroectodermal tumors ( Bobola et al., 2005 Bobola et al., 2005 ; Dumitrache et al., 2018 Dumitrache et al., 2018 ). Mouse embryonic fibroblasts (MEFs) deficient in Polβ are hypersensitive to alkylating agents ( Horton et al., 2003 Horton et al., 2003 ; Poltoratsky et al., 2005 Poltoratsky et al., 2005 ). Interestingly, MMS-induced alkylation damage is tolerated in Polβ -deficient MEF cells after subsequent loss of AAG ( Horton et al., 2003 Horton et al., 2003 ; Poltoratsky et al., 2005 Poltoratsky et al., 2005 ), supporting the importance of proper coordination between BER factors. On the other hand, developing BER inhibitors seems promising for cancer treatment. For example, methoxyamine, one well known clinically used APE inhibitor, has been successful in numerous cancer cell types and tumor xenograft models in combination with alkylating agents ( Taverna et al., 2001 Taverna et al., 2001 ; Liu and Gerson, 2004 Liu and Gerson, 2004 ; Bapat et al., 2010 Bapat et al., 2010 ). Mechanistically, methoxyamine reacts with an aldehyde-sugar group of AP site and forms a stable methoxyamine-AP-intermediate, which blocks the endonuclease activity of APE and disrupts the balance of BER ( Taverna et al., 2001 Taverna et al., 2001 ; Bapat et al., 2010 Bapat et al., 2010 ). Similarly, inhibition of Pol β also unbalances BER and shows promising effects in alkylation chemotherapy. Clinical trial data have suggested that inhibitors of Pol β are effective in combination with temozolomide (TMZ) in colon cancer ( Jaiswal et al., 2009 Jaiswal et al., 2009 , 2011 2011 ). However, both APE1 and Pol β are essential proteins, as loss of either one in mice is embryonic lethal ( Sobol et al., 1996 Sobol et al., 1996 ; Bapat et al., 2009 Bapat et al., 2009 ). Therefore, administration of these inhibitors may also be detrimental to normal cells. To reach a better therapeutic end, poly(ADP-ribose) polymerase (PARP), loss of which is not lethal in mouse models, has emerged as another intriguing target. Although it is still controversial whether PARP participates in the main stage of BER, it has an important role in the proper repair of SSBs and may contribute to the recruitment of XRCC1 complex. Consequently, PARP1 deficiency in both mice and cancer cells causes increased sensitivity to various alkylating agents ( de Murcia et al., 1997 de Murcia et al., 1997 ; Shibata et al., 2005 Shibata et al., 2005 ). Importantly, PARP inhibitors selectively kill cancer cells carrying BRCA mutations or with any other specific alterations ( Rouleau et al., 2010 Rouleau et al., 2010 ). This synthetic lethality effect further helps to dissimilate the drug effects in different tissues and different patients. Notably, alteration in the efficiency of BER may render cancer cells resistant to alkylating agents when combined with PARP inhibitors ( Jelezcova et al., 2010 Jelezcova et al., 2010 ). This seemingly controversial result comes from a break in the driving chain of the toxic intermediates generated during BER. Collectively, these findings help to establish BER modulations as an essential chemotherapeutic option, while also supporting the need for a comprehensive genetic inspection before clinical treatment. 4 MGMT directs the proper repair of O -alkyl lesions 1 Of all the single-methyl lesions induced by commonly used S N 1-type alkylating agents, O -alkyl lesions contribute most to mutagenic and cytotoxic effects in cells. These lesions can be preferentially eliminated through direct reversal by MGMT, which counters the genotoxicity elicited by the intact MMR machinery in cells ( Fig. 3 Fig. 3 ). Together, the leverage between the MGMT expression status and the MMR efficiency drives the carcinogenesis potential of O -alkyl lesions, as well as regulates the response to most of the S N 1-type alkylating agents. 4.1 Direct reversal of O 6 meG by MGMT 2 MGMT reactively transfers the alkyl groups on DNA bases to a cysteine residue in its catalytic pocket. This process is irreversible because it will inactivate the MGMT, which is then subject to degradation ( Fig. 1 Fig. 1 b) ( Kaina et al., 2007 Kaina et al., 2007 ). MGMT targets most of the O -alkyl lesions in cells, with higher preference to O -methyl lesions (such as O 6 meG). Other O -alkyl lesions, such as the O 6 -ethylation of guanine, cause larger distortion of DNA and can also be repaired by the NER or FA pathway. Importantly, there is no significant difference in the repair of O 6 meG in either ssDNA or double-stranded DNA (dsDNA), nor any bias toward the active transcription regions or inactive regions. MGMT is more of a protective but not an essential protein, as knockout of MGMT in mice confers no significant abnormality but shows increased toxicity and a high predisposition to tumors upon treatment with exogenous alkylators ( Glassner et al., 1999 Glassner et al., 1999 ). The protecting effects of MGMT are clearly manifested by alkylation chemotherapy resistance in brain, skin, thymus, and liver cancers with high expression of MGMT ( Christmann et al., 2011 Christmann et al., 2011 ). 4.2 Modulation of the biological effects of O 6 meG by MGMT and MMR 2 O 6 meG lesions are potentially mutagenic and carcinogenic, because they cause significant increases in the G:C to A:T transition ratio during DNA replication ( Warren et al., 2006 Warren et al., 2006 ). Therefore, the overexpression of MGMT has been shown to prevent lymphoma carcinogenesis, even in a cancer-prone mouse model ( Dumenco et al., 1993 Dumenco et al., 1993 ; Liu et al., 1994 Liu et al., 1994 ). Yet the O 6 meG is inherently less cytotoxic; genetic studies substantiated that efficient MMR machinery is required to elicit its cytotoxicity ( Fig. 3 Fig. 3 ). One model explained that the futile cycles of MMR, in which a mispaired nucleotide against an O 6 meG lesion is excised and then resynthesized, eventually lead to replication collapse and trigger the apoptotic response ( York and Modrich, 2006 York and Modrich, 2006 ; Mojas et al., 2007 Mojas et al., 2007 ; Quiros et al., 2010 Quiros et al., 2010 ). Importantly, as an iterative round of MMR requires multiple replication processes, O 6 meG shows high cytotoxicity specifically in proliferating cancer cells ( Roos et al., 2004 Roos et al., 2004 ). However, genetic studies showed that the missense mutations in mutator S homolog 2 ( Msh2 ) or Msh6 , which have normal affinity to the mispair but defect in ATP processing, still confer a normal apoptotic response to several S N 1 alkylating agents ( Lin et al., 2004 Lin et al., 2004 ; Yang et al., 2004 Yang et al., 2004 ). Hence, another model is proposed where the interaction between the MutSα-MutLα complex and ataxia telangiectasia-mutated and Rad3-related (ATR) can directly activate the ATR-ATRIP (ATR-interacting protein) pathway and induce the checkpoint kinase 1 (CHK1) checkpoint; but to what extent these activations alone trigger cell death is currently unclear ( Yoshioka et al., 2006 Yoshioka et al., 2006 ). Perhaps both models work together in cells to elicit cytotoxicity in O 6 meG: while direct signaling initiates the immediate apoptotic responses, the futile cycles of MMR amplify and sustain the cytotoxicity. 4.3 Guidance for S N 1 alkylation chemotherapy by the MGMT expression status 2 In clinic, the expression status of MGMT is an important indicator for diagnosis in several tumors, including glioma and glioblastoma. Determining the epigenetic modification status of the MGMT gene could help to improve the efficacy of clinically used alkylating drugs. For example, the front-line chemotherapeutic drug TMZ has been shown effective in glioma and glioblastoma patients with hypermethylation of the MGMT promoter region ( Esteller et al., 2000 Esteller et al., 2000 ; Hegi et al., 2005 Hegi et al., 2005 ; Christmann et al., 2011 Christmann et al., 2011 ; Butler et al., 2020 Butler et al., 2020 ). In addition, several MGMT inhibitors are utilized in combination with alkylation chemotherapy, such as O 6 -benzylguanine ( O 6 BG), which works by competition with the cellular O 6 meG. Patients with anaplastic glioma demonstrate the effectiveness of O 6 BG in sensitizing cancer cells to TMZ ( Sun et al., 2018 Sun et al., 2018 ; Saha et al., 2020 Saha et al., 2020 ). In addition, MMR efficiency, which accounts for the cytotoxicity of O 6 meG lesion in cells, is another important consideration when exploiting MGMT-dependent chemotherapy. MMR blocking in Mgmt -/- mice reduces the sensitivity toward alkylating agents ( Kawate et al., 2000 Kawate et al., 2000 ; Klapacz et al., 2009 Klapacz et al., 2009 ). In this manner, loss of Msh6 or mutator L homolog 1 ( Mlh1 ) expression by either epigenetic inactivation or mutation may provide instruction for the proper use of chemotherapeutic alkylators, including nitrosourea and TMZ ( Fukushima et al., 2005 Fukushima et al., 2005 ; Hunter et al., 2006 Hunter et al., 2006 ; Xie et al., 2016 Xie et al., 2016 ). Interestingly, whereas loss of MMR efficiency in many colon and gastric cancers is correlated with poor prognosis ( McFaline-Figueroa et al., 2015 McFaline-Figueroa et al., 2015 ), the neo-antigen stem from the increased mutation may guide selective response to immune checkpoint blockage ( Westdorp et al., 2016 Westdorp et al., 2016 ; Germano et al., 2017 Germano et al., 2017 ). 5 Direct reversal of alkylation lesions by the ALKBH demethylase 1 Another direct reversal mechanism to counter alkylation lesions is the reversal of several cytotoxic N -alkyl lesions (such as N 1 meA or N 3 meC) by the ALKBH demethylase family, in a Fe(II) and 2-oxogluterate (2-OG)-dependent reaction ( Fig. 1 Fig. 1 c). To date, nine human ALKBH homologues are known, but only ALKBH2 and ALKBH3 show strong in vitro activity toward alkylated DNA adducts ( Duncan et al., 2002 Duncan et al., 2002 ; Aas et al., 2003 Aas et al., 2003 ). Moreover, spontaneous genomic mutations and N 1 meA lesions accumulated in Alkbh2 -/- mice but not in Alkbh3 -/- mice, suggesting a dominant role for ALKBH2 in reversal of N 1 meA lesions ( Ringvoll et al., 2006 Ringvoll et al., 2006 ). Further studies found that compared to Alkbh2 -/- mice, Alkbh2 -/- Alkbh3 -/- double-knockout mice are more susceptible to alkylating agents, suggesting that both ALKBH2 and ALKBH3 are required for proper alkylation repair in vivo ( Calvo et al., 2012 Calvo et al., 2012 ). A major difference between these two enzymes is the substrate preference. While ALKBH2 prefers a dsDNA context, ALKBH3 prefers an ssDNA substrate ( Aas et al., 2003 Aas et al., 2003 ). Interestingly, the ALKBH3-associated helicase activating signal co-integrator complex 3 (ASCC3) unwinds dsDNA to expose the alkylation lesion, expanding the substrate repertoire for ALKBH3 ( Dango et al., 2011 Dango et al., 2011 ). 5.1 Signal transduction in ALKBH-dependent alkylation repair 2 Repair factor recruitment is essential for proper repair processes. Normally, the substrates for ALKBH proteins are hidden within the DNA double helix, underscoring the importance of a proper recognition mechanism. A possible model for ALKBH2 recruitment has been proposed based on the interaction between PCNA and ALKBH2 through a non-canonical binding motif ( Gilljam et al., 2009 Gilljam et al., 2009 ). Although the inducible interaction and colocalization between PCNA and ALKBH2 in S phase support this theory, knowledge of the detailed coordination and recognition mechanism is still lacking ( Gilljam et al., 2009 Gilljam et al., 2009 ; Fu et al., 2015 Fu et al., 2015 ). Consistent with the ssDNA preference, the recruitment of ALKBH3 may largely depend on the transcription or splicing machinery and the assembly of an ASCC ( Fig. 4 Fig. 4 a). Evidently, deficiency in either one of the above factors impairs ALKBH3 foci formation and sensitizes cells to alkylating agents ( Dango et al., 2011 Dango et al., 2011 ; Brickner et al., 2017 Brickner et al., 2017 , 2019 2019 ; Soll et al., 2018 Soll et al., 2018 ). Additionally, the defects of ALKBH2 foci formation in ASCC2 depletion cells also indicate an overlap in the regulation of ALKBH2 and ALKBH3 recruitment. Moreover, the absence of a ubiquitin-binding domain in ASCC2 diminishes the recruitment of ASCC complex and ALKBH3 to the lesion, suggesting ubiquitin-dependent regulation ( Brickner et al., 2017 Brickner et al., 2017 ). A subsequent proteomic study identified really interesting new gene finger protein 113A (RNF113A) as the major E3 responsible for the generation of the ubiquitin chain recognized by ASCC2 ( Brickner et al., 2017 Brickner et al., 2017 ) ( Fig. 4 Fig. 4 ). Significantly, nonsense mutation in RNF113A has been found to correlate with X-linked trichothiodystrophy (X-TTD) in Caenorhabditis elegans ( Corbett et al., 2015 Corbett et al., 2015 ). Cells from X-TTD human patients show diminished ASCC recruitment and lower cell viability in response to MMS, indicating a link between X-TTD and ALKBH3-dependent alkylation repair ( Brickner et al., 2017 Brickner et al., 2017 ). It is questionable whether ALKBH3 is linked with replication where ssDNA is also available, since ALKBH2 but not ALKBH3 interacts with PCNA on replication forks. Interestingly, studies in Escherichia coli , yeast, and human cells showed that ssDNA-binding proteins recombinase A (RecA) and DNA repair protein RAD51 homolog C (RAD51C) interact with ALKBH3, thus facilitating the recruitment of ALKBH3 at the 3'-tailed DNA generated during HR repair ( Mohan et al., 2019 Mohan et al., 2019 ) ( Fig. 4 Fig. 4 b). However, it remains unclear whether a similar mechanism may also guide ALKBH3 demethylase alkylation lesions at replication forks. 5.2 ALKBH-dependent alkylation repair and cancer chemotherapy 2 Deficiency in ALKBH3 or ASCC3 increases cellular sensitivity to alkylating agents, at least in several prostate or lung cancer cells ( Dango et al., 2011 Dango et al., 2011 ; Brickner et al., 2017 Brickner et al., 2017 ). However, since the substrates for ALKBH proteins are not the major lesions induced by most clinically used alkylating agents, such effects may largely rely on the addiction to an ALKBH-dependent repair pathway in specific tissues or organs ( Dango et al., 2011 Dango et al., 2011 ). Nevertheless, considering that ALKBH2 or ALKBH3 is found to be overexpressed in many types of cancer, including prostate adenocarcinoma, non-small cell lung carcinoma, and head and neck cancer, chemotherapy developed from ALKBH-dependent alkylation repair may be promising ( Konishi et al., 2005 Konishi et al., 2005 ; Gilljam et al., 2009 Gilljam et al., 2009 ; Tasaki et al., 2011 Tasaki et al., 2011 ; Pilžys et al., 2019). Additionally, Stefansson et al. (2017) Stefansson et al. (2017) suggested that promoter methylation status of the ALKBH3 gene in several breast cancers correlates with poor prognosis. In addition, a positive correlation exists between the promoter methylation and cellular N 3 meC levels in several breast cancer cell lines, suggesting a potential direction for alkylation chemotherapy ( Stefansson et al., 2017 Stefansson et al., 2017 ). However, unlike the well-established role for MGMT promoter methylation in glioblastoma chemotherapy, direct evidence to show the promoter methylation status of the ALKBH gene in guiding the cellular response to alkylating agents is still missing. Another key predictor for ALKBH-dependent repair efficiency in cells is 2-hydroxyglutarate (2-HG) ( Wang et al., 2015 Wang et al., 2015 ; Chen et al., 2017 Chen et al., 2017 ). Oncometabolite 2-HG generated in isocitrate dehydrogenase ( IDH ) mutant cells has been shown to inhibit the enzyme activity of ALKBH3 and ALKBH2 in vitro ( Wang et al., 2015 Wang et al., 2015 ; Chen et al., 2017 Chen et al., 2017 ). Consistently, IDH mutant glioma cells exhibit defects in reversal of N 1 meA lesion, resulting in hypersensitivity to the S N 2 alkylating agent MMS ( Wang et al., 2015 Wang et al., 2015 ). It is notable that IDH mutant glioma cells are also hypersensitive to nitrosourea agents including 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea (CCNU), suggesting a broader protective ability of the IDH enzyme against alkylation lesions. Tran et al. (2017) Tran et al. (2017) suggested that cells depleted of glutamine, the precursor of 2-OG, generate more cellular N 1 meA/ N 3 meC lesions, which will ultimately evolve into DSBs. However, other effects elicited by depletion of glutamine in cells, such as an imbalance in nucleotide metabolism, may also contribute to DNA damage ( Fu et al., 2019 Fu et al., 2019 ). Nevertheless, this study indicates new possibilities for using the glutaminase inhibitor 6-diazo-5-oxo-L-norleucine (DON) clinically to sensitize cancer cells, particularly cancers with ALKBH overexpression, to alkylating agents ( Tran et al., 2017 Tran et al., 2017 ). 6 A lesion more than a lesion 1 On the other hand, DNA methylation is an essential epigenetic control mechanism in mammals. Especially, the methylation of the fifth carbon of cytosine produces 5-methylcytosine (5mC), often referred to as the "fifth base" of the DNA code. 5mC is regulatable and programmable and can thus affect genetic information ( Luo et al., 2018 Luo et al., 2018 ). It is interesting to consider whether other DNA adducts may also play a similar role as epigenetic markers in gene transcription or translation. Ample clues exist in the RNA context, where N 1 meA or N 3 meC, generated either enzymatically or non-enzymatically ( Hori, 2014 Hori, 2014 ; Kietrys et al., 2017 Kietrys et al., 2017 ), can block translation and potentially induce ribosomal miscoding ( Safra et al., 2017 Safra et al., 2017 ; Zhao et al., 2017 Zhao et al., 2017 ; Zhang and Jia, 2018 Zhang and Jia, 2018 ). Profiling of the N 1 meA modifications in messenger RNA (mRNA) suggests that they are mostly enriched in the 5'-untranslated region (5'-UTR), a position opposite to that of the well-established regulatory RNA mark N 6 -methyladenine ( N 6 meA) ( Dominissini et al., 2016 Dominissini et al., 2016 ; Li et al., 2016 Li et al., 2016 ; Zhao et al., 2017 Zhao et al., 2017 ). Such a discrepancy in position may indicate a functional compensation between N 6 meA and N 1 meA in RNA. This notion has been further strengthened by the overlap recognition of N 6 meA and N 1 meA through YT521-B homology domain family 2 (YTHDF2) ( Wang et al., 2014 Wang et al., 2014 ; Dai et al., 2018 Dai et al., 2018 ; Seo and Kleiner, 2020 Seo and Kleiner, 2020 ). Other studies suggested that ALKBH3 regulates transfer RNA (tRNA) stability through regulating N 3 meC in tRNA ( Ueda et al., 2017 Ueda et al., 2017 ; Chen et al., 2019 Chen et al., 2019 ). However, the missing information on a bona fide methyltransferase for N 1 meA or N 3 meC in DNA is an obstacle to understanding the regulatory role of N 1 meA or N 3 meC. Nevertheless, the regulatable ALKBH-dependent repair mechanism still provides cells with the means to orchestrate the adducts' profile across the genome. Ideally, the regulatory scenario may present in certain tissues which are under persistent exposure to chemotherapeutic alkylators or where N 1 meA/ N 3 meC is used as a potential biomarker. Future development of related genomic techniques and discovery of more participants may help reveal the potential physiological function of these DNA adducts. 7 Concluding remarks 1 In recent years, tremendous progress has been seen in the understanding of DNA alkylation damage repair. It is important to note that multiple layers of complexity need to be incorporated to get a more complete understanding of the biological effects of DNA alkylation. DNA alkylation responses are variable between cells, tissues, and individuals; therefore, the responses of tumors to alkylating agents are often variable. A better understanding of the regulation of DNA alkylation may provide new opportunities to exploit genomic instability and formulate targeted therapy for cancer cells. Future advancement in deciphering the biological effects elicited by alkylation lesions could be explored through establishing novel proteomic or high through-put genomic technologies. 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Nat Rev Mol Cell Biol , 18 ( 1 ): 31 - 42 . https://doi.org/10.1038/nrm.2016.132 https://doi.org/10.1038/nrm.2016.132 Post-transcriptional gene regulation by mRNA modifications Yihan PENG wrote and edited the manuscript; Huadong PEI designed the study and revised the manuscript. Both authors have read and approved the final manuscript. Therefore, both authors have full access to the data in the study and take responsibility for the integrity and security of the data. 10.1631/jzus.B2000344 1673-1581（2021）01-0047-16 PENG Yihan,PEI Huadong. 2021. DNA alkylation lesion repair: outcomes and implications in cancer chemotherapy. Journal of Zhejiang University-SCIENCE B(Biomedicine & Biotechnology), 22(1):47-62. PENG Yihan,PEI Huadong. 2021. DNA alkylation lesion repair: outcomes and implications in cancer chemotherapy. Journal of Zhejiang University-SCIENCE B(Biomedicine & Biotechnology), 22(1):47-62. 2020-06-25 2020-12-04 2020-12-16 2021-01-15 2022-05-09 2021 Zhejiang University Press Yihan PENG and Huadong PEI declare they have no conflict of interest. This article does not contain any studies with human or animal subjects performed by either of the authors. Compliance with ethics guidelines 浙江大学学报（英文版）（B辑：生物医学和生物技术） 1 22