Karmanos Cancer Institute, Departments of Oncology and Pathology, Wayne State University School of Medicine, 2204, Prentis Building, 110 East Warren Avenue, Detroit, Michigan 48201, USA.
Curr Cancer Drug Targets. 2011 Jun;11(5):613-23. doi: 10.2174/156800911795655921.
The success of current treatment strategies is limited by the development of therapy resistance as evidenced by recurrence of the primary tumor or distant metastasis. Eradication of primary and metastatic disease requires interventions at both the cancer cell and tumor microenvironment levels. In this review, we will discuss mechanisms that are intrinsic to cancer cells, and those that are mediated by the tumor microenvironment as contributors to drug resistance. Mechanisms contributing to multidrug resistance phenotype and the challenges facing molecular targeted therapy are discussed. The DNA damage tolerance pathway confers tolerance to a variety of structurally and functionally unrelated drugs. A rationale for targeting the DNA damage tolerance pathway as a novel tool for overcoming drug resistance is discussed. We have also addressed the need for employing clinically relevant model systems for performing drug sensitivity evaluations. These model systems must take into account the three-dimensional organization and in vivo relationship of tumor with its microenvironment. Such integrative efforts would not only yield a more global understanding of the tumor- and microenvironment-derived mechanisms involved in emergence of drug resistance but would also provide novel therapeutic targets that will disrupt the interactions between the tumor cells and its microenvironment.
目前的治疗策略的成功受到治疗抵抗的发展的限制,这表现在原发性肿瘤的复发或远处转移。根除原发性和转移性疾病需要在癌细胞和肿瘤微环境两个层面进行干预。在这篇综述中,我们将讨论导致药物耐药性的内在癌细胞机制和由肿瘤微环境介导的机制。讨论了导致多药耐药表型的机制以及分子靶向治疗所面临的挑战。DNA 损伤耐受途径赋予了对各种结构和功能上不相关的药物的耐受性。讨论了将 DNA 损伤耐受途径作为克服耐药性的新工具的合理性。我们还探讨了需要采用临床相关的模型系统来进行药物敏感性评估。这些模型系统必须考虑肿瘤与其微环境之间的三维组织和体内关系。这种综合的努力不仅会更全面地了解肿瘤和微环境衍生的机制在药物耐药性的出现,还会提供新的治疗靶点,破坏肿瘤细胞与其微环境之间的相互作用。