角蛋白1在维持B16-F10黑色素瘤细胞系的存活和氧化应激状态中发挥重要作用。

International journal of physiology, pathophysiology and pharmacology Pub Date : 2021-02-15 eCollection Date: 2021-01-01
Yujia Li, Mingchao Zhang, Weihai Ying
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引用次数: 0

摘要

角蛋白在上皮中起着多种重要的生物学作用。角蛋白1 (K1)/角蛋白10 (K10)异源二聚体是角质细胞分化的标志。虽然角蛋白在正常的黑素细胞中不存在,但在黑色素瘤细胞系和人类黑色素瘤中都发现了角蛋白。黑色素瘤细胞中角蛋白的生物学意义尚不清楚。在我们目前的研究中,我们应用K1 siRNA来研究K1在B16-F10黑色素瘤细胞中的生物学意义。我们发现,低至16%的K1水平下降导致细胞凋亡和坏死的显著增加。此外,轻微的K1减少导致细胞中氧化应激的两种指标——二氯荧光素(DCF)和乙二胺信号显著增加。总的来说,我们的发现提供了第一个证据,表明K1在维持黑色素瘤细胞的存活中起关键作用,并且K1在调节细胞的氧化应激状态中起重要作用。这些发现揭示了角蛋白在癌细胞中的新功能,表明K1可能成为黑色素瘤的新治疗靶点。
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Keratin 1 plays significant roles in maintaining the survival and oxidative stress state of B16-F10 melanoma cell lines.

Keratins play multiple significant biological roles in epithelium. Keratin 1 (K1)/keratin 10 (K10) heterodimer is a hallmark for keratinocyte differentiation. While keratins are absent in normal melanocyte, keratins have been found in both melanoma cell lines and human melanoma. The biological significance of the keratins in melanoma cells has remained unclear. In our current study we applied K1 siRNA to investigate the biological significance of K1 in B16-F10 melanoma cells. We found that as low as a 16% decrease in the K1 level led to significant increases in both apoptosis and necrosis of the cells. Moreover, the mild K1 decrease led to significant increases in both dichlorofluorescein (DCF) and ethidium signals - two indicators of oxidative stress - in the cells. Collectively, our findings have provided the first evidence indicating both a critical role of the K1 in maintaining the survival of melanoma cells and an important role of the K1 in modulating the oxidative stress state of the cells. These findings have exposed new functions of keratins in cancer cells, suggesting that K1 may become a novel therapeutic target for melanoma.

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