分化诱导因子-3衍生物抑制PAK1活性和乳腺癌细胞增殖

Peter O. Oladimeji, Y. Kubohara, H. Kikuchi, Y. Oshima, Courtney Rusch, Rebekah Skerl, M. Diakonova
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引用次数: 8

摘要

分化诱导因子1-3 (DIFs - 1-3)是一种在细胞黏菌盘状盘基骨菌中发现的氯化烷基苯类化合物,被认为是抗肿瘤药物,因为它们在体外抑制多种哺乳动物肿瘤细胞的增殖。虽然DIF-1和DIF-3的抗增殖作用已被充分证明,但dif作用的确切分子机制尚未完全阐明。在这项研究中,我们检测了DIFs及其衍生物对PAK1的影响,PAK1是一种关键的丝氨酸-苏氨酸激酶,可被多种配体激活并调节细胞增殖。我们检测了DIF衍生物对细胞中PAK1激酶活性的影响。我们还研究了DIF-3(+1)衍生物对PAK1激酶活性、cyclin D1启动子活性和乳腺癌细胞增殖的影响。发现部分衍生物在人乳腺癌MCF-7细胞中稳定过表达PAK1,强烈抑制PAK1激酶活性。在这些衍生物中,DIF-3(+1)最有效,在体外激酶试验中直接抑制重组纯化PAK1的激酶活性。此外,DIF-3(+1)强烈抑制cyclin D1启动子活性和MCF-7和T47D乳腺癌细胞的增殖,稳定过表达PAK1,以响应催乳素、雌激素、表皮生长因子和heregulin。在本研究中,我们提出PAK1作为DIF-3(+1)的靶点介导其抗增殖作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Derivative of Differentiation-Inducing Factor-3 Inhibits PAK1 Activity and Breast Cancer Cell Proliferation
Differentiation-inducing factors 1-3 (DIFs 1-3), chlorinated alkylphenones identified in the cellular slime mold Dictyostelium discoideum, are considered anti-tumor agents because they inhibit proliferation of a variety of mammalian tumor cells in vitro. Although the anti-proliferative effects of DIF-1 and DIF-3 are well-documented, the precise molecular mechanisms underlying the actions of DIFs have not been fully elucidated. In this study, we examined the effects of DIFs and their derivatives on PAK1, a key serine-threonine kinase, which is activated by multiple ligands and regulates cell proliferation. We examined the effect of DIF derivatives on PAK1 kinase activity in cells. We also examined the effect of DIF-3(+1) derivative on PAK1 kinase activity in vitro, cyclin D1 promoter activity and breast cancer cell proliferation. It was found that some derivatives strongly inhibited PAK1 kinase activity in human breast cancer MCF-7 cells stably over expressing PAK1. Among the derivatives, DIF-3(+1) was most potent, which directly inhibited kinase activity of recombinant purified PAK1 in an in vitro kinase assay. Furthermore, DIF-3(+1) strongly inhibited both cyclin D1 promoter activity and proliferation of MCF-7 and T47D breast cancer cells stably over expressing PAK1 in response to prolactin, estrogen, epidermal growth factor and heregulin. In the present study we propose PAK1 as DIF-3(+1) target mediating its anti-proliferative effect.
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