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
相关论文
共 105 条
[71]  
Pantuck AJ, 2003, CLIN CANCER RES, V9, P4641
[72]   The miR-200 family determines the epithelial phenotype of cancer cells by targeting the E-cadherin repressors ZEB1 and ZEB2 [J].
Park, Sun-Mi ;
Gaur, Arti B. ;
Lengyel, Ernst ;
Peter, Marcus E. .
GENES & DEVELOPMENT, 2008, 22 (07) :894-907
[73]   Searching for the hereditary causes of renal-cell carcinoma [J].
Pavlovich, CP ;
Schmidt, LS .
NATURE REVIEWS CANCER, 2004, 4 (05) :381-393
[74]   The !von Hippel-Lindau tumor suppressor gene product represses oncogenic β-catenin signaling in renal carcinoma cells [J].
Peruzzi, Benedetta ;
Athauda, Gagani ;
Bottaro, Donald P. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (39) :14531-14536
[75]  
Peruzzi Benedetta, 2009, P321, DOI 10.1007/978-1-59745-332-5_14
[76]  
Polascik TJ, 1996, CANCER RES, V56, P1892
[77]   A novel function for tissue inhibitor of metalloproteinases-3 (TIMP3): inhibition of angiogenesis by blockage of VEGF binding to VEGF receptor-2 [J].
Qi, JH ;
Ebrahem, Q ;
Moore, N ;
Murphy, G ;
Claesson-Welsh, L ;
Bond, M ;
Baker, A ;
Anand-Apte, B .
NATURE MEDICINE, 2003, 9 (04) :407-415
[78]   Cystic renal neoplasia following conditional inactivation of Apc in mouse renal tubular epithelium [J].
Qian, CN ;
Knol, J ;
Igarashi, P ;
Lin, FM ;
Zylstra, U ;
Teh, BT ;
Williams, BO .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (05) :3938-3945
[79]   New insights into an enigmatic tumour suppressor [J].
Ratcliffe, PJ .
NATURE CELL BIOLOGY, 2003, 5 (01) :7-8
[80]   Wilms' tumour: Connecting tumorigenesis and organ development in the kidney [J].
Rivera, MN ;
Haber, DA .
NATURE REVIEWS CANCER, 2005, 5 (09) :699-712