Gaggianesi Miriam, Di Franco Simone, Pantina Vincenzo Davide, Porcelli Gaetana, D'Accardo Caterina, Verona Francesco, Veschi Veronica, Colarossi Lorenzo, Faldetta Naida, Pistone Giuseppe, Bongiorno Maria Rita, Todaro Matilde, Stassi Giorgio
Department of Surgical Oncological and Stomatological Sciences (DICHIRONS), University of Palermo, Palermo, Italy.
Department of Health Promotion Sciences, Internal Medicine and Medical Specialties (PROMISE), University of Palermo, Palermo, Italy.
Front Oncol. 2021 Jul 20;11:702642. doi: 10.3389/fonc.2021.702642. eCollection 2021.
Despite the recent advances in cancer patient management and in the development of targeted therapies, systemic chemotherapy is currently used as a first-line treatment for many cancer types. After an initial partial response, patients become refractory to standard therapy fostering rapid tumor progression. Compelling evidence highlights that the resistance to chemotherapeutic regimens is a peculiarity of a subpopulation of cancer cells within tumor mass, known as cancer stem cells (CSCs). This cellular compartment is endowed with tumor-initiating and metastasis formation capabilities. CSC chemoresistance is sustained by a plethora of grow factors and cytokines released by neighboring tumor microenvironment (TME), which is mainly composed by adipocytes, cancer-associated fibroblasts (CAFs), immune and endothelial cells. TME strengthens CSC refractoriness to standard and targeted therapies by enhancing survival signaling pathways, DNA repair machinery, expression of drug efflux transporters and anti-apoptotic proteins. In the last years many efforts have been made to understand CSC-TME crosstalk and develop therapeutic strategy halting this interplay. Here, we report the combinatorial approaches, which perturb the interaction network between CSCs and the different component of TME.
尽管近年来在癌症患者管理和靶向治疗的发展方面取得了进展,但全身化疗目前仍是许多癌症类型的一线治疗方法。在最初出现部分缓解后,患者会对标准治疗产生耐药性,导致肿瘤迅速进展。有力证据表明,对化疗方案的耐药性是肿瘤块内癌细胞亚群(即癌症干细胞,CSCs)的一个特性。这个细胞亚群具有肿瘤起始和转移形成能力。癌症干细胞的化学抗性由邻近肿瘤微环境(TME)释放的大量生长因子和细胞因子维持,肿瘤微环境主要由脂肪细胞、癌症相关成纤维细胞(CAFs)、免疫细胞和内皮细胞组成。肿瘤微环境通过增强生存信号通路、DNA修复机制、药物外排转运蛋白和抗凋亡蛋白的表达,增强癌症干细胞对标准治疗和靶向治疗的耐药性。在过去几年中,人们做出了许多努力来理解癌症干细胞与肿瘤微环境的相互作用,并开发出阻止这种相互作用的治疗策略。在这里,我们报告了一些联合方法,这些方法扰乱了癌症干细胞与肿瘤微环境不同成分之间的相互作用网络。