Oikonomou Eftychia, Koustas Evangelos, Goulielmaki Maria, Pintzas Alexander
Laboratory of Signal Mediated Gene Expression, Institute of Biology, Medicinal Chemistry and Biotechnology, National Hellenic Research Foundation, Athens, 11635, Greece.
Oncotarget. 2014 Dec 15;5(23):11752-77. doi: 10.18632/oncotarget.2555.
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.
随着对肿瘤异质性和基因改变的认识不断增加,这体现了现代癌症管理中进一步实现个性化医疗的必要性。在此,我们研究了RAS和BRAF致癌信号的相似性以及不同作用,并讨论了其在个性化癌症诊断和治疗中的进一步意义。探讨了由这两种致癌基因介导的冗余机制,以及与BRAF相比,RAS对信号通路和基因表达的不同调节。讨论了RAS与BRAF不同功能在包括结直肠癌、黑色素瘤、肺癌等相关肿瘤类型中的意义。将评估当前关于利用RAS - BRAF通路改变开发新型疗法和有效合理联合用药的治疗发现及未来观点,以及针对相关反应标志物的伴随检测。耐药细胞可能也表现出药物依赖性,以至于改变给药剂量可能预防致命性耐药的出现,这一概念构成了主要的治疗障碍。