Laboratory of Pathophysiology, Butantan Institute, São Paulo 05503-900, Brazil.
Department of Pharmacology, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-060, Brazil.
Toxins (Basel). 2021 Nov 22;13(11):830. doi: 10.3390/toxins13110830.
Epithelial-mesenchymal transition (EMT) occurs in the early stages of embryonic development and plays a significant role in the migration and the differentiation of cells into various types of tissues of an organism. However, tumor cells, with altered form and function, use the EMT process to migrate and invade other tissues in the body. Several experimental (in vivo and in vitro) and clinical trial studies have shown the antitumor activity of crotoxin (CTX), a heterodimeric phospholipase A2 present in the venom. In this study, we show that CTX modulates the microenvironment of tumor cells. We have also evaluated the effect of CTX on the EMT process in the spheroid model. The invasion of type I collagen gels by heterospheroids (mix of MRC-5 and A549 cells constitutively prepared with 12.5 nM CTX), expression of EMT markers, and secretion of MMPs were analyzed. Western blotting analysis shows that CTX inhibits the expression of the mesenchymal markers, N-cadherin, α-SMA, and αv. This study provides evidence of CTX as a key modulator of the EMT process, and its antitumor action can be explored further for novel drug designing against metastatic cancer.
上皮-间充质转化(EMT)发生在胚胎发育的早期阶段,在细胞迁移和分化为生物体的各种组织类型中起着重要作用。然而,形态和功能改变的肿瘤细胞利用 EMT 过程迁移并侵袭体内的其他组织。一些实验(体内和体外)和临床试验研究表明,存在于毒液中的异二聚体磷脂酶 A2 蛇毒蛋白(CTX)具有抗肿瘤活性。在这项研究中,我们表明 CTX 调节肿瘤细胞的微环境。我们还评估了 CTX 对球体模型中 EMT 过程的影响。分析了异型球体(MRC-5 和 A549 细胞的混合物,用 12.5 nM CTX 持续制备)对 I 型胶原凝胶的侵袭、EMT 标志物的表达和 MMPs 的分泌。Western blotting 分析表明 CTX 抑制间充质标志物 N-钙黏蛋白、α-SMA 和 αv 的表达。这项研究提供了 CTX 作为 EMT 过程关键调节剂的证据,其抗肿瘤作用可进一步探索用于针对转移性癌症的新型药物设计。