Department of Pathophysiology, Victor Babes University of Medicine and Pharmacy, 300041 Timisoara, Romania.
Biol Chem. 2013 Jun;394(6):773-81. doi: 10.1515/hsz-2013-0106.
Betulinic acid (BA) exhibits antitumoral activity by blocking proliferation, invasion, and angiogenesis. However, the impact of BA on epithelial-to-mesenchymal transition (EMT), a hallmark of cancer metastasis induced among others by neutrophil gelatinase-associated lipocalin (NGAL), remains unknown. The present study aimed at determining the effect of BA on NGAL-induced EMT. In A375 melanoma cells, BA downregulated mesenchymal markers, increased epithelial markers, and inhibited cytoskeletal reorganization. In addition, BA limited endogenous NGAL production and further suppressed EMT induced by exogenously added NGAL and the corresponding invasive cellular phenotype. In conclusion, BA interferes with EMT-associated changes, a mechanism to antagonize invasive melanoma cells.
桦木酸 (BA) 通过阻断增殖、侵袭和血管生成来发挥抗肿瘤活性。然而,BA 对上皮间质转化 (EMT) 的影响尚不清楚,EMT 是癌症转移的一个标志,除其他因素外,还可被中性粒细胞明胶酶相关脂质运载蛋白 (NGAL) 诱导。本研究旨在确定 BA 对 NGAL 诱导的 EMT 的影响。在 A375 黑色素瘤细胞中,BA 下调间充质标志物,增加上皮标志物,并抑制细胞骨架重排。此外,BA 限制内源性 NGAL 的产生,并进一步抑制由外源性添加的 NGAL 诱导的 EMT 和相应的侵袭细胞表型。总之,BA 干扰 EMT 相关变化,是拮抗侵袭性黑色素瘤细胞的一种机制。