Mass spectrometry analysis of intact protein <italic style="font-style: italic">N</italic>-glycosylation signatures of cells and sera in pancreatic adenocarcinomas

Mingming XU; Zhaoliang LIU; Wenhua HU; Ying HAN; Zhen WU; Sufeng CHEN; Peng XIA; Jing DU; Xumin ZHANG; Piliang HAO; Jun XIA; Shuang YANG

doi:10.1631/jzus.B2200652

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Mass spectrometry analysis of intact protein N-glycosylation signatures of cells and sera in pancreatic adenocarcinomas

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Research Article | Updated：2023-12-27

Mass spectrometry analysis of intact protein N-glycosylation signatures of cells and sera in pancreatic adenocarcinomas
Mass spectrometry analysis of intact protein N-glycosylation signatures of cells and sera in pancreatic adenocarcinomas
胰腺癌细胞和血清完整蛋白质N-糖基化特征的质谱分析
Journal of Zhejiang University-SCIENCE B (Biomedicine & Biotechnology) Vol. 25, Issue 1, Pages: 51-64(2024)
Affiliations：

1.Center for Clinical Mass Spectrometry, College of Pharmaceutical Sciences, Soochow University, Suzhou 215123, China
2.School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China
3.State Key Laboratory of Genetic Engineering, Department of Biochemistry, School of Life Sciences, Fudan University, Shanghai 200438, China
4.Department of Clinical Laboratory Center, Zhejiang Provincial People’s Hospital, People’s Hospital of Hangzhou Medical College, Hangzhou 310014, China
Funds：
DOI：10.1631/jzus.B2200652
CLC：
CSTR：

徐明明,刘兆亮,胡文华等.胰腺癌细胞和血清完整蛋白质N-糖基化特征的质谱分析[J].浙江大学学报（英文版）（B辑：生物医学和生物技术）,2024,25(01):51-64.

Mingming XU, Zhaoliang LIU, Wenhua HU, et al. Mass spectrometry analysis of intact protein N-glycosylation signatures of cells and sera in pancreatic adenocarcinomas. [J]. Journal of Zhejiang University-SCIENCE B (Biomedicine & Biotechnology) 25(1):51-64(2024)
徐明明,刘兆亮,胡文华等.胰腺癌细胞和血清完整蛋白质N-糖基化特征的质谱分析[J].浙江大学学报（英文版）（B辑：生物医学和生物技术）,2024,25(01):51-64. DOI： 10.1631/jzus.B2200652.

Mingming XU, Zhaoliang LIU, Wenhua HU, et al. Mass spectrometry analysis of intact protein N-glycosylation signatures of cells and sera in pancreatic adenocarcinomas. [J]. Journal of Zhejiang University-SCIENCE B (Biomedicine & Biotechnology) 25(1):51-64(2024) DOI： 10.1631/jzus.B2200652.

摘要

胰腺癌作为最恶性的癌症之一，早期干预是提高生存率的关键。目前尚无可靠的方法对其发展为恶性肿瘤进行早期识别，因此在胰腺肿瘤发生过程中发现早期分子变化的要求迫在眉睫。异常糖基化与癌症进展密切相关，对将糖基化变化作为胰腺癌诊断的生物标记物已有较多研究，但详细的糖组学信息，尤其是胰腺癌在药物治疗前后的位点特异性,N,-糖基化变化研究，仍需进一步深入。本研究采用综合性固相化学酶糖组学手段，对胰腺癌细胞和患者血清中的聚糖、糖基化位点和完整糖肽展开分析。癌症细胞中,N,-聚糖的分析结果显示，原位肿瘤MIA PaCa-2细胞分泌的糖蛋白增加，然而含有较多分泌糖蛋白的人类血清在其特定糖基化位点上的聚糖却发生了显著变化。上述结果表明，肿瘤特异性糖基化可作为胰腺癌诊断的潜在生物标志物。此外，本研究发现抗,KRAS, G12C突变的小分子抑制剂AMG-510可显著降低MIA PaCa-2细胞的糖基化水平，这表明,KRAS,在细胞糖基化过程中发挥抑制作用，将有助于AMG-510的抗肿瘤作用。

Abstract

Pancreatic cancer is among the most malignant cancers, and thus early intervention is the key to better survival outcomes. However, no methods have been derived that can reliably identify early precursors of development into malignancy. Therefore, it is urgent to discover early molecular changes during pancreatic tumorigenesis. As aberrant glycosylation is closely associated with cancer progression, numerous efforts have been made to mine glycosylation changes as biomarkers for diagnosis; however, detailed glycoproteomic information, especially site-specific ,N,-glycosylation changes in pancreatic cancer with and without drug treatment, needs to be further explored. Herein, we used comprehensive solid-phase chemoenzymatic glycoproteomics to analyze glycans, glycosites, and intact glycopeptides in pancreatic cancer cells and patient sera. The profiling of ,N,-glycans in cancer cells revealed an increase in the secreted glycoproteins from the primary tumor of MIA PaCa-2 cells, whereas human sera, which contain many secreted glycoproteins, had significant changes of glycans at their specific glycosites. These results indicated the potential role for tumor-specific glycosylation as disease biomarkers. We also found that AMG-510, a small molecule inhibitor against Kirsten rat sarcoma viral oncogene homolog (,KRAS,) G12C mutation, profoundly reduced the glycosylation level in MIA PaCa-2 cells, suggesting that ,KRAS, plays a role in the cellular glycosylation process, and thus glycosylation inhibition contributes to the anti-tumor effect of AMG-510.

关键词

胰腺癌糖基化生物标志物糖蛋白组学质谱

Keywords

Pancreatic cancerGlycosylationBiomarkerGlycoproteomicsMass spectrometry

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Research Unit of Precision Pathologic Diagnosis in Tumors of the Oral and Maxillofacial Regions, Chinese Academy of Medical Sciences (2019RU)

Central Laboratory, Peking University School and Hospital of Stomatology

Department of Oral Pathology, Peking University School and Hospital of Stomatology / National Center of Stomatology / National Clinical Research Center for Oral Diseases / National Engineering Research Center of Oral Biomaterials and Digital Medical Devices

Key Laboratory of Tropical Translational Medicine of Ministry of Education, College of Biomedical Information and Engineering, Hainan Women and Children’s Medical Center, Hainan Medical University

College of Bioinformatics Science and Technology, Harbin Medical University

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Mass spectrometry analysis of intact protein N-glycosylation signatures of cells and sera in pancreatic adenocarcinomas

Mass spectrometry analysis of intact protein N-glycosylation signatures of cells and sera in pancreatic adenocarcinomas

DOI：10.1631/jzus.B2200652

摘要

Abstract

关键词

Keywords

references