| Literature DB >> 28262927 |
Afsane Bahrami1, Seyed Mahdi Hassanian2,3, Soodabeh ShahidSales4, Zahra Farjami1, Malihe Hasanzadeh5, Kazem Anvari4, Amir Aledavood4, Mina Maftouh2, Gordon A Ferns6, Majid Khazaei7, Amir Avan2,4.
Abstract
The V-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog (KRAS) is frequently dysregulated in colorectal cancer (CRC). It is involved in the modulation of several downstream effectors, that include: Raf/Mek/Erk, PI3K/Akt, RalGDS/p38MAPK, and Rac/Rho, and thereby influences tumorigenesis, the invasive behaviors of tumor cell, and resistance to therapy. There is growing evidence exploring the use of drugs that target these pathways in the treatment of CRC. Cetuximab has been approved for CRC patients without a KRAS mutation, or for EGFR-expressing metastatic CRC, although some of the patients have a mutation of KRAS and NRAS. This review summarizes the recent knowledge about the therapeutic potential of targeting RAS with particular emphasis on recent preclinical and clinical studies in treatment of CRC.Entities:
Keywords: KRAS; cetuximab; colorectal cancer; novel anticancer agent
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Year: 2017 PMID: 28262927 DOI: 10.1002/jcp.25890
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384