Transcriptomic Meta-Analysis Identifies Upregulated Clotting and Fibrinolysis Pathways in Colorectal Cancer Tumors Containing Hereditary PMS2 Mismatch Repair Deficiency.

Autor:	Gibson TM; Microbiology and Molecular Biology, Brigham Young University, Provo, Utah, United States., Spendlove MD; Microbiology and Molecular Biology, Brigham Young University, Provo, Utah, United States., Rapier-Sharman N; Microbiology and Molecular Biology, Brigham Young University, Provo, Utah, United States., Pickett BE; Microbiology and Molecular Biology, Brigham Young University.
Jazyk:	angličtina
Zdroj:	MicroPublication biology [MicroPubl Biol] 2024 Jul 27; Vol. 2024. Date of Electronic Publication: 2024 Jul 27 (Print Publication: 2024).
DOI:	10.17912/micropub.biology.001159
Abstrakt:	Lynch Syndrome is characterized by deficient mismatch repair (dMMR) components. We performed a meta-analysis of multiple RNA-sequencing datasets from patients with different dMMR variants (PMS2, MLH1, and MSH2) to better characterize the unique transcriptional profiles. Our results reveal enriched signaling pathways from tumor samples with germline mutations in the PMS2 gene including upregulation in pathways related to intrinsic and extrinsic prothrombin activation, fibrinolysis, and uPA/uPAR-mediated signaling. These pathways have been associated with tumor growth, invasiveness, and metastasis. This work provides support for further exploration into the role of PMS2 in tumor development, and as a potential therapeutic mechanism. Competing Interests: The authors declare that there are no conflicts of interest present. (Copyright: © 2024 by the authors.)
Databáze:	MEDLINE
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