» Articles » PMID: 22128289

An Overview of the C-MET Signaling Pathway

Overview
Specialty Oncology
Date 2011 Dec 1
PMID 22128289
Citations 393
Authors
Affiliations
Soon will be listed here.
Abstract

c-MET is a receptor tyrosine kinase that, after binding with its ligand, hepatocyte growth factor, activates a wide range of different cellular signaling pathways, including those involved in proliferation, motility, migration and invasion. Although c-MET is important in the control of tissue homeostasis under normal physiological conditions, it has also been found to be aberrantly activated in human cancers via mutation, amplification or protein overexpression. This paper provides an overview of the c-MET signaling pathway, including its role in the development of cancers, and provides a rationale for targeting the pathway as a possible treatment option.

Citing Articles

Network pharmacology and experimental analysis reveal Ethyl caffeate delays osimertinib resistance in lung cancer by suppression of MET.

Sang S, Han Y, Zhou H, Kang X, Gong Y Cancer Cell Int. 2025; 25(1):99.

PMID: 40089772 DOI: 10.1186/s12935-025-03690-5.


Spatial Transcriptomic Analysis of Surgical Resection Specimens of Primary Head and Neck Squamous Cell Carcinoma Treated with Afatinib in a Window-of-Opportunity Study (EORTC90111-24111).

Beyaert S, Loriot A, Machiels J, Schmitz S Int J Mol Sci. 2025; 26(5).

PMID: 40076457 PMC: 11898532. DOI: 10.3390/ijms26051830.


Proteomic characterization of MET-amplified esophageal adenocarcinomas reveals enrichment of alternative splicing- and androgen signaling-related proteins.

Grothey B, Lyu S, Quaas A, Simon A, Jung J, Schroder W Cell Mol Life Sci. 2025; 82(1):112.

PMID: 40074836 PMC: 11904063. DOI: 10.1007/s00018-025-05635-7.


Targeting Heat Shock Transcription Factor 4 Enhances the Efficacy of Cabozantinib and Immune Checkpoint Inhibitors in Renal Cell Carcinoma.

Saito S, Yoshino H, Yokoyama S, Tominaga M, Li G, Arima J Int J Mol Sci. 2025; 26(4).

PMID: 40004241 PMC: 11855069. DOI: 10.3390/ijms26041776.


Emerging Targeted Therapies in Non-Small-Cell Lung Cancer (NSCLC).

Mina S, Shanshal M, Leventakos K, Parikh K Cancers (Basel). 2025; 17(3).

PMID: 39941723 PMC: 11816067. DOI: 10.3390/cancers17030353.


References
1.
Houldsworth J, Cordon-Cardo C, Ladanyi M, Kelsen D, Chaganti R . Gene amplification in gastric and esophageal adenocarcinomas. Cancer Res. 1990; 50(19):6417-22. View

2.
Bhowmick N, Neilson E, Moses H . Stromal fibroblasts in cancer initiation and progression. Nature. 2004; 432(7015):332-7. PMC: 3050735. DOI: 10.1038/nature03096. View

3.
Hiscox S, Hallett M, Puntis M, Nakamura T, Jiang W . Expression of the HGF/SF receptor, c-met, and its ligand in human colorectal cancers. Cancer Invest. 1997; 15(6):513-21. DOI: 10.3109/07357909709047592. View

4.
Miller C, Lin L, Casper A, Lim J, Thomas D, Orringer M . Genomic amplification of MET with boundaries within fragile site FRA7G and upregulation of MET pathways in esophageal adenocarcinoma. Oncogene. 2005; 25(3):409-18. DOI: 10.1038/sj.onc.1209057. View

5.
Forbes S, Bhamra G, Bamford S, Dawson E, Kok C, Clements J . The Catalogue of Somatic Mutations in Cancer (COSMIC). Curr Protoc Hum Genet. 2008; Chapter 10:Unit 10.11. PMC: 2705836. DOI: 10.1002/0471142905.hg1011s57. View