| Literature DB >> 31475898 |
Fengqian Chen1, Martin P Alphonse2, Yan Liu3, Qi Liu2.
Abstract
Over the past decades, designing therapeutic strategies to target KRAS-mutant cancers, which is one of the most frequent mutant oncogenes among all cancer types, have proven unsuccessful regardless of many concerted attempts. There are key challenges for KRAS-mutant anticancer therapy, as the complex cellular processes involved in KRAS signaling has present. Herein, we highlight the emerging therapeutic approaches for inhibiting KRAS signaling and blocking KRAS functions, in hope to serve as a more effective guideline for future development of therapeutics. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.Entities:
Keywords: Anticancer therapeutics; Cell signaling; Guanosine triphosphate-bound RAS; KRAS mutant; KRAS pathway; Oncogene.
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Year: 2019 PMID: 31475898 DOI: 10.2174/1568026619666190902151307
Source DB: PubMed Journal: Curr Top Med Chem ISSN: 1568-0266 Impact factor: 3.295