Oncogenic KRAS regulates BMP4 expression in colon cancer cell lines
Author(s) -
Eva–Maria Duerr,
Yusuke Mizukami,
Kentaro Moriichi,
Manish Gala,
Won-Seok Jo,
Hirotoshi Kikuchi,
Ramnik J. Xavier,
Daniel C. Chung
Publication year - 2012
Publication title -
ajp gastrointestinal and liver physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.644
H-Index - 169
eISSN - 1522-1547
pISSN - 0193-1857
DOI - 10.1152/ajpgi.00047.2011
Subject(s) - kras , downregulation and upregulation , cancer research , biology , mapk/erk pathway , kinase , bone morphogenetic protein 4 , oncogene , microbiology and biotechnology , pi3k/akt/mtor pathway , cancer , signal transduction , colorectal cancer , bone morphogenetic protein , genetics , cell cycle , gene
Activating mutations in the KRAS oncogene are common in colorectal cancer. However, the complete spectrum of KRAS targets that mediate its tumorigenic effect has not yet been fully delineated. We identified bone morphogenetic protein 4 (Bmp4), a transforming growth factor-β family member that regulates development and tissue homeostasis, as a new target of KRAS. In SW480, Hela, and 293 cells, oncogenic KRAS(V12) downregulated BMP4 RNA levels, a BMP4 promoter luciferase construct, and Bmp4 protein levels. The MEK inhibitor PD98059 but not the phosphatidylinositol 3-kinase inhibitor LY294002 blocked this downregulation of BMP4. To identify the region of the BMP4 promoter that mediated this regulation by KRAS, serial 5'-deletions of the promoter were generated. An inhibitory region was identified between -3,285 and -3,258 bp in the Bmp4 promoter. In summary, oncogenic KRAS can downregulate Bmp4 through a transcriptional pathway that depends on ERK. These findings point to a unique link between two pathways that are frequently altered in colon cancer.
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