Boudreault Julien, Wang Ni, Ghozlan Mostafa, Lebrun Jean-Jacques
Cancer Research Program, Department of Medicine, Research Institute of McGill University Health Center, Montreal, QU H4A 3J1, Canada.
Cancers (Basel). 2024 Jan 3;16(1):224. doi: 10.3390/cancers16010224.
The secreted protein transforming growth factor-beta (TGFβ) plays essential roles, ranging from cell growth regulation and cell differentiation in both normal and cancer cells. In melanoma, TGFβ acts as a potent tumor suppressor in melanoma by blocking cell cycle progression and inducing apoptosis. In the present study, we found TGFβ to regulate cancer stemness in melanoma through the Smad signaling pathway. We discovered that TGFβ/Smad signaling inhibits melanosphere formation in multiple melanoma cell lines and reduces expression of the CD133+ cancer stem cell subpopulation in a Smad3-dependent manner. Using preclinical models of melanoma, we further showed that preventing Smad3/4 signaling, by means of CRISPR knockouts, promoted both tumorigenesis and lung metastasis in vivo. Collectively, our results define new functions for the TGFβ/Smad signaling axis in melanoma stem-cell maintenance and open avenues for new therapeutic approaches to this disease.
分泌蛋白转化生长因子-β(TGFβ)发挥着重要作用,涵盖正常细胞和癌细胞中的细胞生长调控与细胞分化。在黑色素瘤中,TGFβ通过阻断细胞周期进程和诱导凋亡,作为黑色素瘤中的一种强大肿瘤抑制因子发挥作用。在本研究中,我们发现TGFβ通过Smad信号通路调节黑色素瘤中的癌症干性。我们发现TGFβ/Smad信号以Smad3依赖的方式抑制多种黑色素瘤细胞系中的黑素球形成,并降低CD133 +癌症干细胞亚群的表达。使用黑色素瘤的临床前模型,我们进一步表明,通过CRISPR基因敲除阻止Smad3/4信号传导,在体内促进肿瘤发生和肺转移。总体而言,我们的结果确定了TGFβ/Smad信号轴在黑色素瘤干细胞维持中的新功能,并为该疾病的新治疗方法开辟了途径。