T-oligo诱导晚期前列腺癌细胞凋亡。

Munirathinam Gnanasekar, Sivasakthivel Thirugnanam, Guoxing Zheng, Aoshuang Chen, Kalyanasundaram Ramaswamy
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引用次数: 16

摘要

前列腺癌是男性中最常见的恶性肿瘤。随着癌症从雄激素敏感期发展到激素难治期,它对雄激素消融治疗产生抗药性。在这个阶段,需要有效的诱导细胞凋亡的新疗法来治疗前列腺癌。同源于端粒3'悬垂(T-oligo)的DNA寡核苷酸可诱导几种人类癌细胞凋亡。在本研究中,我们研究了T-oligo对前列腺癌细胞的影响。我们的研究表明,雄激素非依赖性DU-145细胞在抑制增殖方面对T-oligo敏感。此外,T-oligo诱导DU-145细胞发生凋亡。因此,我们的结果为进一步研究T-oligo作为前列腺癌,特别是雄激素不依赖型前列腺癌的新治疗方法的潜在应用提供了鼓舞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
T-oligo induces apoptosis in advanced prostate cancer cells.

Prostate cancer is the most frequently diagnosed malignancy in men. As cancer progresses from an androgen-sensitive stage to hormone-refractory stage, it turns resistant to androgen ablation therapy. At this stage, effective newer therapies that induce apoptosis are needed for treatment of prostate cancer. DNA oligonucleotides homologous to the telomere 3' overhang (T-oligo) induce apoptosis in several human cancer cells. In the present study, we studied the effect of T-oligo on prostate cancer cells. Our studies showed that androgen-independent DU-145 cells are sensitive to T-oligo in terms of inhibition of proliferation. Moreover, T-oligo induced DU-145 cells to undergo apoptosis. Therefore, our results are encouraging for further investigation in the potential application of T-oligo as a novel therapeutic approach for prostate cancer, especially the androgen-independent.

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Oligonucleotides
Oligonucleotides 生物-生化与分子生物学
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