Signaling pathways in renal cell carcinoma

被引:187
作者
Banumathy, Gowrishankar
Cairns, Paul [1 ]
机构
[1] Fox Chase Canc Ctr, Dept Surg Oncol, Philadelphia, PA 19111 USA
关键词
RCC; signaling pathways; kinases; mTOR; targeted therapy; genetics; epigenetics; TYROSINE KINASE INHIBITOR; ENDOTHELIAL GROWTH-FACTOR; BETA-CATENIN; KIDNEY CANCER; MET PROTOONCOGENE; TARGETED THERAPY; GENE-EXPRESSION; MIR-200; FAMILY; PROMOTER HYPERMETHYLATION; MESENCHYMAL TRANSITION;
D O I
10.4161/cbt.10.7.13247
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Renal cell carcinoma (RCC), the most lethal type of genitourinary cancer, is generally resistant to chemotherapy and radiation therapy. Surgical excision of the tumor at a localized stage remains the mainstay for curative therapy. A number of drugs developed in recent years have shown limited to significant efficacy in treating RCC. These drugs act by blocking critical signaling pathways associated with RCC tumor growth and survival and angiogenesis. Beyond well-validated signaling targets such as VHL, VEGFR and mTOR, additional pathways including HGF/c-MET and Wnt/beta-catenin have emerged as important to RCC pathogenesis. Mutations in one or more components of these signaling networks may affect tumor response to therapy. This review summarizes the state of knowledge about signaling pathways in RCC and discusses the known genetic and epigenetic alterations that underlie dysregulation of these pathways.
引用
收藏
页码:658 / 664
页数:7
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