| Literature DB >> 33982211 |
Shumpei Ohnami1, Kouji Maruyama2, Kai Chen3, Yu Takahashi2, Keiichi Hatakeyama4, Keiichi Ohshima4, Yuji Shimoda5,6, Ai Sakai5,6, Fukumi Kamada5, Sou Nakatani5, Akane Naruoka7, Sumiko Ohnami5, Masatoshi Kusuhara8, Yasuto Akiyama9, Hiroyasu Kagawa3, Akio Shiomi3, Takeshi Nagashima5,6, Kenichi Urakami5, Ken Yamaguchi10.
Abstract
Despite the frequent detection of KRAS driver mutations in patients with colorectal cancer (CRC), no effective treatments that target mutant KRAS proteins have been introduced into clinical practice. In this study, we identified potential effector molecules, based on differences in gene expression between CRC patients carrying wild-type KRAS (n = 390) and those carrying KRAS mutations in codon 12 (n = 240). CRC patients with wild-type KRAS harboring mutations in HRAS, NRAS, PIK3CA, PIK3CD, PIK3CG, RALGDS, BRAF, or ARAF were excluded from the analysis. At least 11 promising candidate molecules showed greater than two-fold change between the KRAS G12 mutant and wild-type and had a Benjamini-Hochberg-adjusted P value of less than 1E-08, evidence of significantly differential expression between these two groups. Among these 11 genes examined in cell lines transfected with KRAS G12 mutants, BMP4, PHLDA1, and GJB5 showed significantly higher expression level in KRAS G12A, G12D, and G12V transfected cells than in the wild-type transfected cells. We expect that this study will lead to the development of novel treatments that target signaling molecules functioning with KRAS G12-driven CRC.Entities:
Keywords: BMP4; Colorectal cancer; KRAS mutation; PHLDA1; Therapeutic targets
Year: 2021 PMID: 33982211 DOI: 10.1007/s11010-021-04172-8
Source DB: PubMed Journal: Mol Cell Biochem ISSN: 0300-8177 Impact factor: 3.396