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Antitumor activity of SA12, a novel peptide, on SKBr-3 breast cancer cells via the mitochondrial apoptosis pathway

机译:SA12,一种新型肽,通过线粒体凋亡途径对SKBr-3乳腺癌细胞的抗肿瘤活性

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Abstract: Breast cancer is considered to be the most common malignancy in women. Treatment of breast cancer has been focused on molecular targeted therapy, and anticancer peptides are considered to be some of the most promising candidate drugs. In the current study, we used mRNA-peptide display technology to screen antibreast cancer peptides and identified a novel peptide, SA12, which showed significant activity in the inhibition of proliferation and induction of apoptosis in SKBr-3 breast cancer cells. The mechanism by which SA12 peptide triggers apoptosis was further investigated using a pull-down assay, reverse transcription-polymerase chain reaction, and Western blotting analysis. The results demonstrated that this peptide could interact with tumor-associated proteins MECP2 and CDC20B, which further induced apoptosis of tumor cells via the mitochondrial pathway involving the Bcl-2 family and related caspases. We propose that the novel SA12 peptide has the potential to provide a new strategy for the development of targeted therapy in breast cancer.
机译:摘要:乳腺癌被认为是女性最常见的恶性肿瘤。乳腺癌的治疗一直集中在分子靶向治疗上,抗癌肽被认为是最有前途的候选药物。在本研究中,我们使用mRNA肽展示技术筛选抗乳腺癌肽,并鉴定出一种新型肽SA12,该肽在抑制SKBr-3乳腺癌细胞的增殖和诱导细胞凋亡方面显示出显着的活性。使用下拉测定,逆转录聚合酶链反应和蛋白质印迹分析进一步研究了SA12肽触发凋亡的机制。结果表明,该肽可与肿瘤相关蛋白MECP2和CDC20B相互作用,进一步通过涉及Bcl-2家族和相关胱天蛋白酶的线粒体途径诱导肿瘤细胞凋亡。我们建议新型SA12肽有潜力为乳腺癌靶向治疗的发展提供新的策略。

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