Therapeutic Targets of KRAS in Colorectal Cancer

被引:10
|
作者
Rahman, Shafia [1 ]
Garrel, Shimon [2 ]
Gerber, Michael [3 ]
Maitra, Radhashree [1 ,3 ]
Goel, Sanjay [1 ]
机构
[1] Montefiore Med Ctr, Albert Einstein Coll Med, Dept Med Oncol, 1695 Eastchester Rd Bronx, New York, NY 10461 USA
[2] Lander Coll Men, Dept Biol, 75-31 150th St, New York, NY 11367 USA
[3] Yeshiva Univ, Dept Biol, 500 West 185th St, New York, NY 10033 USA
关键词
colorectal cancer; KRAS mutation; targeted therapy; TYROSINE PHOSPHATASE SHP-2; SIGNAL-REGULATED KINASE; MUTANT KRAS; ANTITUMOR-ACTIVITY; TUMOR-GROWTH; G-QUADRUPLEX; RAS; INHIBITOR; ACTIVATION; MUTATIONS;
D O I
10.3390/cancers13246233
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Colorectal cancer is among the most common cancers in the United States. The advancement in treatment and early diagnosis have enabled a reduction in mortality from the disease among the patients with early and localized disease; however, the survival continues to be dismal in the metastatic colorectal cancers. Understanding the biological and genetic factors is crucial is making the therapeutic strategy and improving survival outcomes. One of such critical steps is the understanding of the mechanism and development of therapeutic targets against metastatic colorectal cancers bearing the KRAS mutation. Patients with metastatic colorectal cancer have a 5-year overall survival of less than 10%. Approximately 45% of patients with metastatic colorectal cancer harbor KRAS mutations. These mutations not only carry a predictive role for the absence of response to anti-EGFR therapy, but also have a negative prognostic impact on the overall survival. There is a growing unmet need for a personalized therapy approach for patients with KRAS-mutant colorectal cancer. In this article, we focus on the therapeutic strategies targeting KRAS- mutant CRC, while reviewing and elaborating on the discovery and physiology of KRAS.
引用
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页数:14
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