Your browser doesn't support javascript.
loading
Targeting Mutant KRAS for Anticancer Therapy.
Chen, Fengqian; Alphonse, Martin P; Liu, Yan; Liu, Qi.
Afiliação
  • Chen F; Department of Environmental Toxicology, The Institute of Environmental and Human Health (TIEHH), Texas Tech University, Lubbock, TX 79416, United States.
  • Alphonse MP; Department of Dermatology, Johns Hopkins University School of Medicine, Cancer Research Building II, Suite 216, 1550 Orleans Street, Baltimore, MD 21231, United States.
  • Liu Y; Western University of Health Sciences, 309 E. Second Street, Pomona, CA 91766, United States.
  • Liu Q; Department of Dermatology, Johns Hopkins University School of Medicine, Cancer Research Building II, Suite 216, 1550 Orleans Street, Baltimore, MD 21231, United States.
Curr Top Med Chem ; 19(23): 2098-2113, 2019.
Article em En | MEDLINE | ID: mdl-31475898
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.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína Oncogênica p21(ras) / Proteínas Proto-Oncogênicas p21(ras) / Neoplasias / Antineoplásicos Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína Oncogênica p21(ras) / Proteínas Proto-Oncogênicas p21(ras) / Neoplasias / Antineoplásicos Idioma: En Ano de publicação: 2019 Tipo de documento: Article