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Role of Heparan Sulfate 2-O-Sulfotransferase in Prostate Cancer Cell Proliferation, Invasion, and Growth Factor Signaling

机译:硫酸乙酰肝素2-O-磺基转移酶在前列腺癌细胞增殖,侵袭和生长因子信号转导中的作用

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Heparan-sulfate proteoglycans (HSPGs) are required for maximal growth factor signaling in prostate cancer progression. The degree of sulfate modification on the covalently attached heparan sulfate (HS) chains is one of the determining factors of growth factor-HSPG interactions. Sulfate groups are transferred to HS chains via a series of O-sulfotransferases. In the present study, we demonstrate that Heparan sulfate 2-O-sulfotransferase (2OST) is essential for maximal proliferation and invasion of prostate cancer cells in the LNCaP-C4-2B model. We also show that a decrease in invasion due to 2OST siRNA is associated with an increase in actin and E-cadherin accumulation at the cell surface. 2OST expression correlates with increasing metastatic potential in this model. We demonstrate that 2OST expression is upregulated by the stress-inducible transcription factors HIF1α, ATF2, and NFκB. Chromatin immunoprecipitation analysis suggests that HIF1αand ATF2 act directly on the 2OST promoter, while NFκB acts indirectly.
机译:前列腺癌进展中最大的生长因子信号转导需要乙酰肝素硫酸蛋白聚糖(HSPG)。共价连接的硫酸乙酰肝素(HS)链上的硫酸盐修饰程度是生长因子-HSPG相互作用的决定因素之一。硫酸基团通过一系列O-磺基转移酶转移至HS链。在本研究中,我们证明了硫酸乙酰肝素2-O-磺基转移酶(2OST)对于LNCaP-C4-2B模型中前列腺癌细胞的最大增殖和侵袭至关重要。我们还表明,归因于2OST siRNA的侵袭减少与肌动蛋白和E-钙粘蛋白在细胞表面积累的增加有关。 2OST表达与该模型中转移潜力的增加相关。我们证明2OST表达被应激诱导的转录因子HIF1α,ATF2和NFκB上调。染色质免疫沉淀分析表明,HIF1α和ATF2直接作用于2OST启动子,而NFκB间接作用。

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