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BRAF Vs RAS Oncogenes: Are Mutations of the Same Pathway Equal? Differential Signalling and Therapeutic Implications

Overview
Journal Oncotarget
Specialty Oncology
Date 2014 Nov 1
PMID 25361007
Citations 53
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Abstract

As the increased knowledge of tumour heterogeneity and genetic alterations progresses, it exemplifies the need for further personalized medicine in modern cancer management. Here, the similarities but also the differential effects of RAS and BRAF oncogenic signalling are examined and further implications in personalized cancer diagnosis and therapy are discussed. Redundant mechanisms mediated by the two oncogenes as well as differential regulation of signalling pathways and gene expression by RAS as compared to BRAF are addressed. The implications of RAS vs BRAF differential functions, in relevant tumour types including colorectal cancer, melanoma, lung cancer are discussed. Current therapeutic findings and future viewpoints concerning the exploitation of RAS-BRAF-pathway alterations for the development of novel therapeutics and efficient rational combinations, as well as companion tests for relevant markers of response will be evaluated. The concept that drug-resistant cells may also display drug dependency, such that altered dosing may prevent the emergence of lethal drug resistance posed a major therapy hindrance.

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References
1.
Kambara T, Simms L, Whitehall V, Spring K, Wynter C, Walsh M . BRAF mutation is associated with DNA methylation in serrated polyps and cancers of the colorectum. Gut. 2004; 53(8):1137-44. PMC: 1774130. DOI: 10.1136/gut.2003.037671. View

2.
Rampazzo E, Bertorelle R, Serra L, Terrin L, Candiotto C, Pucciarelli S . Relationship between telomere shortening, genetic instability, and site of tumour origin in colorectal cancers. Br J Cancer. 2010; 102(8):1300-5. PMC: 2856015. DOI: 10.1038/sj.bjc.6605644. View

3.
Solit D, Garraway L, Pratilas C, Sawai A, Getz G, Basso A . BRAF mutation predicts sensitivity to MEK inhibition. Nature. 2005; 439(7074):358-62. PMC: 3306236. DOI: 10.1038/nature04304. View

4.
Kikuchi H, Pino M, Zeng M, Shirasawa S, Chung D . Oncogenic KRAS and BRAF differentially regulate hypoxia-inducible factor-1alpha and -2alpha in colon cancer. Cancer Res. 2009; 69(21):8499-506. PMC: 2811371. DOI: 10.1158/0008-5472.CAN-09-2213. View

5.
Oikonomou E, Makrodouli E, Evagelidou M, Joyce T, Probert L, Pintzas A . BRAF(V600E) efficient transformation and induction of microsatellite instability versus KRAS(G12V) induction of senescence markers in human colon cancer cells. Neoplasia. 2009; 11(11):1116-31. PMC: 2767214. DOI: 10.1593/neo.09514. View