Department of Cancer Physiology, H Lee Moffitt Cancer Center and Research Institute, Tampa, FL 33612, USA.
Department of Molecular Medicine, The Scripps Research Institute, Jupiter, FL 33458, USA.
Cancer Cell. 2020 Apr 13;37(4):471-484. doi: 10.1016/j.ccell.2020.03.007.
Advances in our understanding of molecular mechanisms of tumorigenesis have translated into knowledge-based therapies directed against specific oncogenic signaling targets. These therapies often induce dramatic responses in susceptible tumors. Unfortunately, most advanced cancers, including those with robust initial responses, eventually acquire resistance to targeted therapies and relapse. Even though immune-based therapies are more likely to achieve complete cures, acquired resistance remains an obstacle to their success as well. Acquired resistance is the direct consequence of pre-existing intratumor heterogeneity and ongoing diversification during therapy, which enables some tumor cells to survive treatment and facilitates the development of new therapy-resistant phenotypes. In this review, we discuss the sources of intratumor heterogeneity and approaches to capture and account for it during clinical decision making. Finally, we outline potential strategies to improve therapeutic outcomes by directly targeting intratumor heterogeneity.
我们对肿瘤发生分子机制的认识的进步已经转化为针对特定致癌信号靶点的基于知识的治疗方法。这些疗法通常会在易感肿瘤中引起显著的反应。不幸的是,大多数晚期癌症,包括那些最初反应强烈的癌症,最终会对靶向治疗产生耐药性并复发。尽管免疫疗法更有可能实现完全治愈,但获得性耐药仍然是其成功的障碍。获得性耐药是肿瘤内异质性的直接后果,也是治疗过程中持续多样化的结果,这使得一些肿瘤细胞能够在治疗中存活,并促进新的治疗耐药表型的发展。在这篇综述中,我们讨论了肿瘤内异质性的来源,以及在临床决策中捕获和考虑这些异质性的方法。最后,我们概述了通过直接靶向肿瘤内异质性来改善治疗效果的潜在策略。