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首页> 外文期刊>Cellular Physiology and Biochemistry >Chronic leptin treatment sensitizes MCF-7 breast cancer cells to estrogen
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Chronic leptin treatment sensitizes MCF-7 breast cancer cells to estrogen

机译:慢性瘦素治疗可使MCF-7乳腺癌细胞对雌激素敏感

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摘要

Obesity is associated with an increased risk of estrogen-dependent breast cancer. The adipokine leptin, whose levels are chronically increased in obese people, has been shown to stimulate ER positive cancer cell growth. Considering previous evidence of a crosstalk between leptin and estrogen signaling, the objective of this study was to establish the influence of chronic leptin treatment on estrogen-dependent cell growth. Methods: To this aim, we use the estrogen receptor (ER) positive MCF-7 breast cancer cell line treated chronically with leptin and analyzed estrogen-dependent cell growth, ERs (ERα and ERβ) expression, ER-dependent transcriptional activity as well as cell survival to the antiestrogenic agents tamoxifen and ICI 182,780. Results: Leptin signaling pathway kept activated after chronic stimulation (7 days) with leptin showing significant phosphorylation of JAK2 and STAT3 and higher cell proliferation rate. Chronic leptin at 100 ng/mL dose increased ERα to ERβ ratio and consistently enhanced estrogen-dependent transcriptional activity, increasing E2-dependent cell growth and resistance to antiestrogen agents. Conclusion: This study supports the existence of a crosstalk between leptin and estrogen, in which leptin might play an important role potentiating the mitogenic action of estrogen, probably by alteration of ERα to ERβ ratio.
机译:肥胖与雌激素依赖性乳腺癌的风险增加有关。在肥胖人群中,脂肪因子瘦素的水平长期升高,已被证明能刺激ER阳性癌细胞的生长。考虑到瘦素与雌激素信号转导之间相互干扰的证据,本研究的目的是确定长期瘦素治疗对雌激素依赖性细胞生长的影响。方法:为此,我们使用长期用瘦素处理的雌激素受体(ER)阳性MCF-7乳腺癌细胞系,分析了雌激素依赖性细胞生长,ERs(ERα和ERβ)的表达,ER依赖性转录活性以及抗雌激素药物他莫昔芬和ICI 182,780的细胞存活率。结果:长期刺激(7天)后,瘦素显示出JAK2和STAT3显着磷酸化,并具有较高的细胞增殖速率,从而激活了瘦素信号传导途径。浓度为100 ng / mL的慢性瘦素可增加ERα与ERβ的比率,并持续增强雌激素依赖性转录活性,增强E2依赖性细胞生长和对抗雌激素剂的抵抗力。结论:这项研究支持瘦素与雌激素之间的串扰,瘦素可能在增强雌激素的促有丝分裂作用中起重要作用,可能是通过改变ERα与ERβ的比例来实现的。

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