The HGF-cMET signaling pathway in conferring stromal-induced BRAF-inhibitor resistance in melanoma

被引:9
|
作者
Filitis, Dan C. [1 ]
Rauh, Jake [2 ]
Mahalingam, Meera [3 ]
机构
[1] Dartmouth Hitchcock Med Ctr, Dermatol Sect, Lebanon, NH 03766 USA
[2] Dartmouth Coll, Hanover, NH 03755 USA
[3] VA Med Ctr, Dept Pathol & Lab Med, West Roxbury, MA 02132 USA
关键词
HGF-cMET signaling pathway; melanoma; resistance; stromal-induced BRAF-inhibitor; HEPATOCYTE GROWTH-FACTOR; FACTOR SCATTER FACTOR; MET PROTOONCOGENE PRODUCT; TUMOR CYTOTOXIC FACTOR; C-MET; METASTATIC MELANOMA; HUMAN KERATINOCYTES; MALIGNANT-MELANOMA; MOLECULAR-CLONING; HUMAN FIBROBLASTS;
D O I
10.1097/CMR.0000000000000194
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Genetic heterogeneity in melanoma is well established. Given this, as well as the complexity of mechanisms involved in cancer in vivo, a more complete understanding of the development of resistance requires a closer look at the tumor ecosystem, including the microenvironment. Echoing this more comprehensive approach, a number of recent studies on BRAF-inhibitor resistance have brought our attention back to the tumor microenvironment, particularly through a focus on HGF-cMET signaling - a known means of stromal-parenchymal communication. Our review focuses on the results of these recent investigations, and through a review of relevant HGF-cMET past literature looks to provide a context by which to better understand the role of stromal-parenchymal signaling in BRAF resistance/melanoma progression. Copyright (C) 2015 Wolters Kluwer Health, Inc. All rights reserved.
引用
收藏
页码:470 / 478
页数:9
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