Vanderbilt-Ingram Cancer Center, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA 02114, USA.
Cancer Cell. 2014 Mar 17;25(3):282-303. doi: 10.1016/j.ccr.2014.02.025.
ERBB receptors were linked to human cancer pathogenesis approximately three decades ago. Biomedical investigators have since developed substantial understanding of the biology underlying the dependence of cancers on aberrant ERBB receptor signaling. An array of cancer-associated genetic alterations in ERBB receptors has also been identified. These findings have led to the discovery and development of mechanism-based therapies targeting ERBB receptors that have improved outcome for many cancer patients. In this Perspective, we discuss current paradigms of targeting ERBB receptors with cancer therapeutics and our understanding of mechanisms of action and resistance to these drugs. As current strategies still have limitations, we also discuss challenges and opportunities that lie ahead as basic scientists and clinical investigators work toward more breakthroughs.
大约三十年前,人们发现 ERBB 受体与人类癌症的发病机制有关。此后,生物医学研究人员深入了解了癌症对异常 ERBB 受体信号的依赖的生物学基础。还发现了 ERBB 受体中一系列与癌症相关的遗传改变。这些发现促使人们发现并开发了针对 ERBB 受体的基于机制的治疗方法,从而改善了许多癌症患者的预后。在本观点文章中,我们讨论了用癌症疗法靶向 ERBB 受体的当前范例,以及我们对这些药物的作用机制和耐药性的理解。由于当前的策略仍然存在局限性,因此我们还讨论了基础科学家和临床研究人员在朝着更多突破努力时所面临的挑战和机遇。