Belhabib Ismahane, Zaghdoudi Sonia, Lac Claire, Bousquet Corinne, Jean Christine
Centre de Recherche en Cancérologie de Toulouse (CRCT), INSERM U1037, Université Toulouse III Paul Sabatier, ERL5294 CNRS, 31037 Toulouse, France.
Cancers (Basel). 2021 Jul 11;13(14):3466. doi: 10.3390/cancers13143466.
Solid cancer progression is dictated by neoplastic cell features and pro-tumoral crosstalks with their microenvironment. Stroma modifications, such as fibroblast activation into cancer-associated fibroblasts (CAFs) and extracellular matrix (ECM) remodeling, are now recognized as critical events for cancer progression and as potential therapeutic or diagnostic targets. The recent appreciation of the key, complex and multiple roles of the ECM in cancer and of the CAF diversity, has revolutionized the field and raised innovative but challenging questions. Here, we rapidly present CAF heterogeneity in link with their specific ECM remodeling features observed in cancer, before developing each of the impacts of such ECM modifications on tumor progression (survival, angiogenesis, pre-metastatic niche, chemoresistance, etc.), and on patient prognosis. Finally, based on preclinical studies and recent results obtained from clinical trials, we highlight key mechanisms or proteins that are, or may be, used as potential therapeutic or diagnostic targets, and we report and discuss benefits, disappointments, or even failures, of recently reported stroma-targeting strategies.
实体癌的进展由肿瘤细胞特征及其与微环境的促肿瘤相互作用所决定。基质修饰,如成纤维细胞激活为癌症相关成纤维细胞(CAFs)和细胞外基质(ECM)重塑,现在被认为是癌症进展的关键事件以及潜在的治疗或诊断靶点。最近对ECM在癌症中的关键、复杂和多重作用以及CAF多样性的认识,彻底改变了该领域并提出了创新但具有挑战性的问题。在这里,我们先快速介绍与在癌症中观察到的特定ECM重塑特征相关的CAF异质性,然后阐述这种ECM修饰对肿瘤进展(生存、血管生成、前转移微环境、化疗耐药性等)以及患者预后的各种影响。最后,基于临床前研究和从临床试验中获得的最新结果,我们强调已被或可能被用作潜在治疗或诊断靶点的关键机制或蛋白质,并报告和讨论最近报道的基质靶向策略的益处、失望之处甚至失败案例。