首页> 外文期刊>International journal of biological sciences >Ilamycin E, a natural product of marine actinomycete, inhibits triple-negative breast cancer partially through ER stress-CHOP-Bcl-2
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Ilamycin E, a natural product of marine actinomycete, inhibits triple-negative breast cancer partially through ER stress-CHOP-Bcl-2

机译:ilamycine是海洋放射素瘤的天然产物,抑制了部分通过ER应激切换-BCL-2的三阴性乳腺癌

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Breast cancer is the most commonly diagnosed cancer and the leading cause of cancer death among women in the worldwide. Triple-negative breast cancer (TNBC) has a poor clinical outcome. The antitumor efficacy of Ilamycins, natural products with anti-tuberculosis activity isolated from deep sea-derived Streptomyces atratus, in TNBC has not been investigated, and the mechanisms remain elusive. Here, we demonstrated that Ilamycin-E, but not -F, decreases cell viability, inhibits G1/S cell cycle progression, and promotes apoptosis in the TNBC cell lines HCC1937 and MDA-MB-468. Ilamycin E promotes apoptosis via activation of endoplasmic reticulum (ER) stress, increasing the expression of CHOP, and down-regulating the expression of anti-apoptotic protein Bcl-2. Depletion of CHOP or overexpression of Bcl2 significantly rescued Ilamycin E-induced apoptosis. These findings indicate that Ilamycin E has anti-cancer activity in TNBC.
机译:乳腺癌是世界上最常见的癌症和癌症死亡的主要原因。三阴性乳腺癌(TNBC)临床结果不佳。钛霉素,天然产物的抗肿瘤效果与来自深海衍生的链霉菌atratus分离的抗结核活性,在TNBC中尚未得到调查,并且机制仍然难以捉摸。在此,我们证明伊霉素-E但不是-F,降低细胞活力,抑制G1 / S细胞周期进展,并促进TNBC细胞系HCC1937和MDA-MB-468中的细胞凋亡。 ilamycin E通过活化的内质网(ER)应激促进细胞凋亡,增加了碎片的表达,降低抗凋亡蛋白Bcl-2的表达。 BCL2的切碎或过表达的耗尽显着拯救了伊霉素E诱导的细胞凋亡。这些发现表明,ILAMYCIN E在TNBC具有抗癌活性。

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