2020
DOI: 10.1016/j.jbo.2020.100315
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c-Met expression in renal cell carcinoma with bone metastases

Abstract: Highlights Bone is a common metastatic site in renal cell carcinoma (RCC). HGF/c-Met pathway is particularly relevant in tumors with bone metastases. c-Met/HGF pathway is involved in RCC progression, conferring poor prognosis. Several c-Met targeting therapies are currently in clinical development. c-Met expression is an important therapeutic target in RCC with bone metastases.

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Cited by 14 publications
(8 citation statements)
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References 101 publications
(127 reference statements)
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“…142 RTKs play a crucial role in maintaining the characteristics of CSCs, such as self-renewal capacity, viability, invasiveness, and tumorigenicity. Several RTKs have been identified to be involved in CSC maintenance, including Eph receptor, 143 MET, 144 EGFR, 145 and others. Taking MET as an example, it is primarily expressed in stem and progenitor cells in normal tissues, while its expression is absent in cells that possess the ability to differentiate.…”
Section: Rtks As Stem Cell Markersmentioning
confidence: 99%
“…142 RTKs play a crucial role in maintaining the characteristics of CSCs, such as self-renewal capacity, viability, invasiveness, and tumorigenicity. Several RTKs have been identified to be involved in CSC maintenance, including Eph receptor, 143 MET, 144 EGFR, 145 and others. Taking MET as an example, it is primarily expressed in stem and progenitor cells in normal tissues, while its expression is absent in cells that possess the ability to differentiate.…”
Section: Rtks As Stem Cell Markersmentioning
confidence: 99%
“… 97 MET is a proto-oncogene encoding c-Met, and the activation of c-Met promotes the development of tumor cells, which is an important mechanism for cancer development. 98 Angiopoietin/Tie-2 signaling promotes the blood vessels within the tumor tissue, and Tie-2 is specifically expressed in endothelial cells. 99 Angiopoietin/Tie2 and MET pathways promote tumor angiogenesis, metastasis, and macrophage infiltration.…”
Section: Combined Treatmentmentioning
confidence: 99%
“…77 A known hypoxia-inducible factor (HIF-1) downstream target, c-Met, is activated by hepatocyte growth factor binding and induces tumorigenesis via mitogenactivated protein kinase, PI3K, and signal transducer and activator of transcription 3 (STAT3) signaling. 78,79 It is also involved in immune microenvironment modulation through the recruitment of neutrophils, driving an inflammatory immunosuppressive environment and inducing PD-L1 expression. 78,79 Cabozantinib, a multitargeted TKI with activity against c-Met, is approved for the treatment of mRCC, both as a single agent and in combination with nivolumab.…”
Section: Systemic Therapy Biologic Insights and Implications For Therapymentioning
confidence: 99%
“…78,79 It is also involved in immune microenvironment modulation through the recruitment of neutrophils, driving an inflammatory immunosuppressive environment and inducing PD-L1 expression. 78,79 Cabozantinib, a multitargeted TKI with activity against c-Met, is approved for the treatment of mRCC, both as a single agent and in combination with nivolumab. 7,80,81 The CABRAMET phase 2 study is currently evaluating the efficacy of cabozantinib in mRCC BM (Clini calTr ials.gov identifier NCT03967522).…”
Section: Systemic Therapy Biologic Insights and Implications For Therapymentioning
confidence: 99%