Activation of SphK2 contributes to adipocyte-induced EOC cell proliferation.

IF 1.6
Open medicine (Warsaw, Poland) Pub Date : 2022-01-31 eCollection Date: 2022-01-01 DOI:10.1515/med-2022-0422
Lan Dai, Chen Wang, Wenjing Wang, Keqi Song, Taiyang Ye, Jie Zhu, Wen Di
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Abstract

Epithelial ovarian cancer (EOC) is the leading cause of deaths due to cancer in women. Adipocytes have been suggested to play a key role in the stimulation of EOC growth. However, the mechanisms underlying the adipocyte-induced EOC proliferation remain undefined. Here, we provide the first evidence that adipocytes induce the activation of sphingosine kinase (SphK) 2 in EOC, which represents a novel pathway that mediates the adipocyte-induced EOC growth. SphK2 inhibition in EOC cells led to a remarkable inhibition of the adipocyte-induced cell proliferation. Moreover, the adipocyte-induced SphK2 activation in EOC cells was extracellular signal-regulated protein kinases (ERK) dependent. Furthermore, silencing SphK2 in EOC significantly inhibited the adipocyte-induced expression of phospho-ERK and c-Myc, two crucial players in EOC growth. Collectively, the current study unraveled a previously unrecognized role of SphK2 in the adipocyte-induced growth-promoting action in EOC, suggesting a novel target for EOC treatment.

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SphK2的激活有助于脂肪细胞诱导的EOC细胞增殖。
上皮性卵巢癌(EOC)是妇女因癌症死亡的主要原因。脂肪细胞被认为在刺激EOC生长中起关键作用。然而,脂肪细胞诱导EOC增殖的机制尚不清楚。在这里,我们提供了第一个证据,证明脂肪细胞在EOC中诱导鞘氨醇激酶(SphK) 2的激活,这代表了一种介导脂肪细胞诱导的EOC生长的新途径。在EOC细胞中抑制SphK2可显著抑制脂肪细胞诱导的细胞增殖。此外,脂肪细胞诱导的SphK2在EOC细胞中的激活依赖于细胞外信号调节蛋白激酶(ERK)。此外,在EOC中沉默SphK2可显著抑制脂肪细胞诱导的磷酸化erk和c-Myc的表达,这两种蛋白在EOC生长中起着至关重要的作用。总的来说,目前的研究揭示了SphK2在脂肪细胞诱导的EOC促生长作用中以前未被认识到的作用,提出了EOC治疗的新靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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