PreprintCited by 67Esophageal Cancer Research and TreatmentAdvanced Proteomics Techniques and ApplicationsGastric Cancer Management and Outcomes

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Integrative proteogenomic characterization of early esophageal cancer

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Preprint — published as 10.1038/s41467-023-37440-w · Paper page

Abstract

We performed a comprehensive genomic, proteomic, and phosphoproteomic analysis of 756 trace-tumor-samples from 124 esophageal cancer (EC) patients, covering 9 major histopathological stages and 22 substages. The results revealed a significant diversity of proteome patterns in the 22 substages. The integrated multi-omics data identified genomic-proteomic aberrations revealing the association of TP53, ATM, and EP400 mutations that affected cell cycle, DNA repair, and glycolysis, with poor prognosis. Proteome-based analysis elucidated the stage-specific molecular characterization and defined the cancer-driving waves along with the mutation accumulation in esophageal carcinogenesis and progression. Furthermore, the trajectory analysis identified 6 major tracks related to different clinical features during early EC progression. Growingly enhanced and hyperphosphorylated phosphoglycerate kinase 1 (PGK1, S203) was detected and considered as a drug target in EC progression. Collectively, this study provides insight into the understanding of the molecular mechanism of EC progression and a valuable resource for the development of therapeutic targets.

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Metadata

Authors
Li, L., Jiang, D., Zhang, Q., Liu, H., Qin, Z., Xu, F., Shen, D., Wang, H., Feng, J., Liu, Y., Chen, W., Zhang, X., Bai, L., Tian, S., Tan, S., Xu, C., Song, Q., Liu, Y., Zhong, Y., Chen, T., Zhou, P., Zhao, J.-Y., Hou, Y.-Y., & Ding, C.
Affiliations
  • Fudan University (CN)
  • Southwest Medical University (CN)
  • Institute of Biomedical Sciences, Human Phenome Institute, Fudan University
  • Fudan University
  • Shanghai Jiao Tong University (CN)
Corresponding author
  • Chen, Tianyin
  • Zhou, Pinghong
Venue
Nature Communications
Published
2021-03-01
Volume
14
Issue
1
Pages
1666-1666
ISSN
2041-1723 (ISSN-L)
OpenAlex
W4360949193
Cited by
67
References
1
Citations by year
2026: 13 · 2025: 28 · 2024: 19 · 2023: 7
FWCI
17.89
Type
journal article
Language
en
Open access
Locations
  • Nature Communications (publishedVersion, cc-by)
  • Research Square (acceptedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • RePEc: Research Papers in Economics (submittedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • Natural Science Foundation of Shanghai (81702372, 18ZR1406800, 2017SHZDZX01)
  • National Natural Science Foundation of China (31972933, 973 Program, 2018YFA0507501, 2012CB910300, 2016YFA0502500, 18ZR1406800, 2017YFA0505100, 81702372, 2014CBA02000, 2014DFB30010, 22XD1420100, 2017SHZDZX01, 31700682, 31270822, 31770886)
  • Ministry of Science and Technology of the People's Republic of China (2014DFB30010, 2016YFA0502500, 2014CBA02000, 2012CB910300, 973 Program)
  • Shanghai Education Development Foundation (19SG02)
  • Shanghai Municipal Education Commission (19SG02)
  • National High-tech Research and Development Program
  • National Key Research and Development Program of China (2016YFA0502500, 2014CBA02000, 2012CB910300)
  • Program of Shanghai Academic Research Leader (22XD1420100)
Topics
  • Health Sciences › Medicine › Surgery › Esophageal Cancer Research and Treatment
  • Physical Sciences › Chemistry › Spectroscopy › Advanced Proteomics Techniques and Applications
  • Health Sciences › Medicine › Oncology › Gastric Cancer Management and Outcomes
Keywords
esophageal squamous cell carcinoma, early esophageal cancer, tumor progression, intraepithelial neoplasia, proteogenomics, multi-omics, alcohol consumption, chromosome 3q gain, TP53 mutation, DNA replication, AKAP9, glycolysis, Wnt signaling, therapeutic target
MeSH terms
Proteogenomics, Esophageal Squamous Cell Carcinoma, Carcinoma, Squamous Cell, Esophageal Neoplasms, Humans, Mutation

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