Borriello Lucia, DeClerck Yves A
Département de pédiatrie, de biochimie et biologie moléculaire - Keck school of medicine, university of Southern California, États-Unis - Children's hospital Los Angeles, 4650 Sunset Boulevard CA 90027 Los Angeles, California, États-Unis.
Med Sci (Paris). 2014 Apr;30(4):445-51. doi: 10.1051/medsci/20143004021. Epub 2014 May 5.
Over the last decade, it has become clear that cancer is not just a disease of the genes, and that the tumor microenvironment (TME) plays an important role in cancer progression. Interactions between tumor cells and the TME, made of the extracellular matrix (ECM) and of non-transformed cells (designated here as stromal cells), promote cancer cell survival and drug resistance. Many of the mechanisms involved are known and are either contact-dependent or contact-independent. Contact between tumor cells and the ECM or stromal cells as well as the production of soluble factors and microvesicles all contribute. The bone marrow plays a special role in environment-mediated drug resistance as it is not only a sanctuary protecting tumor cells from cytotoxic drugs, but also a source of many stromal cells that colonize primary tumors and contribute to the pre-metastatic niche. As our understanding of the mechanisms by which the tumor microenvironment promotes therapeutic resistance progresses, clinical trials testing agents that disrupt the interaction between tumor cells and the stroma have been initiated. This new avenue of therapy is promising.
在过去十年中,有一点已经很明确,即癌症不仅仅是一种基因疾病,而且肿瘤微环境(TME)在癌症进展中起着重要作用。肿瘤细胞与由细胞外基质(ECM)和未转化细胞(在此称为基质细胞)组成的TME之间的相互作用,促进癌细胞的存活和耐药性。许多涉及的机制是已知的,并且要么是接触依赖性的,要么是接触非依赖性的。肿瘤细胞与ECM或基质细胞之间的接触以及可溶性因子和微泡的产生都有作用。骨髓在环境介导的耐药性中起特殊作用,因为它不仅是保护肿瘤细胞免受细胞毒性药物影响的避难所,而且是许多基质细胞的来源,这些基质细胞定植于原发性肿瘤并促成转移前生态位。随着我们对肿瘤微环境促进治疗耐药性机制的理解不断深入,已经启动了测试破坏肿瘤细胞与基质之间相互作用的药物的临床试验。这种新的治疗途径很有前景。