4.3 Article

Proteome biology of primary colorectal carcinoma and corresponding liver metastases

期刊

NEOPLASIA
卷 23, 期 12, 页码 1240-1251

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.neo.2021.10.005

关键词

Colorectal cancer; liver metastases; proteomics; mass spectrometry

类别

资金

  1. Deutsche Forschungsgemeinschaft (DFG) [SCHI 871/17-1, NY 90/6-1, SCHI 871/15-1, GR 4553/5-1, PA 2807/3-1, 431984000 -SFB 1453, 441891347 -SFB 1479, 423813989/GRK2606, INST 39/766-3, 89986987 -SFB 850, 280163318 -FOR 2438]
  2. ERA PerMed programs (BMBF) [01KU1916, 01KU1915A]
  3. German-Israel Foundation [1444]
  4. German Consortium for Translational Cancer Research (project Impro-Rec)
  5. Baden-Wurttemberg Ministry of Science, Research and Art
  6. University of Freiburg

向作者/读者索取更多资源

Colorectal adenocarcinomas predominantly metastasize to the liver, impacting patient survival rates. By comparing the proteome of primary CRC and CRC-LM, distinct biological processes were revealed. This study contributes to a more comprehensive understanding of the biological differences between primary CRC and their corresponding liver metastases.
Colorectal adenocarcinomas (CRC) are one of the most commonly diagnosed tumors worldwide. Colorectal adenocarcinomas primarily metastasize into the liver and (less often) into the peritoneum. Patients suffering from CRC-liver metastasis (CRC-LM) typically present with a dismal overall survival compared to non-metastasized CRC patients. The metastasis process and metastasis promoting factors in patients with CRC are under intensive debate. However, CRC studies investigating the proteome biology are lacking. Formalin-fixed paraffin-embedded (FFPE) tissue specimens provide a valuable resource for comprehensive proteomic studies of a broad variety of clinical malignancies. The presented pilot study compares the proteome of primary CRC and patient-matched CRC-LM. The applied protocol allows a reproducible and straightforward identification and quantification of over 2,600 proteins within the dissected tumorous tissue. Subsequent unsupervised clustering reveals distinct proteome biologies of the primary CRC and the corresponding CRC-LM. Statistical analysis yields multiple differentially abundant proteins in either primary CRC or their corresponding liver metastases. A more detailed analysis of dysregulated biological processes suggests an active immune response in the liver metastases, including several proteins of the complement system. Proteins with structural roles, e.g. cytoskeleton organization or cell junction assembly appear to be less prominent in liver metastases as compared to primary CRC. Immunohistochemistry corroborates proteomic high expression levels of metabolic proteins in CRC-LM. We further assessed how the in vitro inhibition of two in CRC-LM enriched metabolic proteins affected cell proliferation and chemosensitivity. The presented proteomic investigation in a small clinical cohort promotes a more comprehensive understanding of the distinct proteome biology of primary CRC and their corresponding liver metastases.

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