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GT75 aptamer against eukaryotic elongation factor 1A as potential anticancer drug for castrate-resistant prostate cancer (CRPC).

机译:抗真核生物延伸因子1A的GT75适体作为去势抵抗性前列腺癌(CRPC)的潜在抗癌药。

摘要

Prostate cancer diagnosis is increasing, being the second most frequently cancer in men worldwide. The treatment of castrate-resistant prostate cancer is often unsuccessfully and new therapeutic interventions are searching for. Nucleic acid aptamers targeting eEF1A proteins are emerging molecular tools for the control of cancer growth. We found that an aptamer named GT75 was able to bind to eEF1A proteins of human prostate cancer cell lines and to significantly and specifically reduce their growth with respect to the control oligomer CT75. The highest anti-proliferation effect was found in the androgen-independent PC-3 cells. Interestingly, GT75 was able to specifically inhibit the migration of PC-3 cells but not that of the nontumorigenic PZHPV-7 cells. The overall results suggest that the GT75 aptamer targeting eEF1A proteins is a promising molecular drug to develop for the control of the castrate-resistant prostate cancer
机译:前列腺癌的诊断正在增加,是全世界男性中第二常见的癌症。去势抵抗性前列腺癌的治疗通常是不成功的,并且正在寻找新的治疗干预措施。靶向eEF1A蛋白的核酸适体是控制癌症生长的新兴分子工具。我们发现,名为GT75的适体能够与人前列腺癌细胞系的eEF1A蛋白结合,并相对于对照低聚物CT75显着且特异性地降低其生长。在非雄激素依赖性PC-3细胞中发现了最高的抗增殖作用。有趣的是,GT75能够特异性抑制PC-3细胞的迁移,但不能抑制非致瘤性PZHPV-7细胞的迁移。总体结果表明,靶向eEF1A蛋白的GT75适体是一种有望用于控制去势抵抗性前列腺癌的分子药物

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