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多西他赛与奥曲肽协同组合对激素和药物抵抗性前列腺癌细胞中生长因子的调控

Regulation of growth factors in hormone- and drug-resistant prostate cancer cells by synergistic combination of docetaxel and octreotide.

作者信息

Erten Cigdem, Karaca Burcak, Kucukzeybek Yuksel, Gorumlu Gurbuz, Cengiz Ercument, Gul Mustafa K, Atmaca Harika, Uzunoglu Selim, Karabulut Bulent, Sanli Ulus A, Uslu Ruchan

机构信息

Division of Medical Oncology, Tulay Aktas Oncology Hospital, Turkey.

出版信息

BJU Int. 2009 Jul;104(1):107-14. doi: 10.1111/j.1464-410X.2009.08340.x. Epub 2009 Feb 3.

Abstract

OBJECTIVE To evaluate the effects of combined treatment with docetaxel and octreotide, a somatostatin analogue, on human hormone- and drug-refractory prostate cancer cell lines, PC-3 and DU-145, and on some growth factors related to tumour growth and angiogenesis in prostate cancer. MATERIALS AND METHODS A cell proliferation assay was used to assess the cytotoxicity of the drugs. To verify apoptosis, both DNA fragmentation (by enzyme-linked immunosorbent assay) and caspase 3/7 activity were measured. We also investigated the effect of combined docetaxel and octreotide on growth factors secreted from prostate cancer cells using a human growth factor antibody array. RESULTS The combination of docetaxel and octreotide resulted in significant synergistic cytotoxic activity and apoptosis, which was dose- and time-dependent. The combined treatment also resulted in significantly less secretion of stem cell factor and platelet-derived growth factor-AB in PC-3 cells, and transforming growth factor-beta and basic fibroblast growth factor in DU-145 cells, than in untreated controls. CONCLUSION Octreotide, a somatostatin analogue, combined with docetaxel might provide a rationale treatment option for hormone-refractory prostate cancer cells, not only by direct inhibition of cell proliferation but also by inhibiting the secretion of growth factors.

摘要

目的 评估多西他赛与生长抑素类似物奥曲肽联合治疗对人激素难治性及药物难治性前列腺癌细胞系PC-3和DU-145的影响,以及对前列腺癌中一些与肿瘤生长和血管生成相关的生长因子的影响。材料与方法 采用细胞增殖试验评估药物的细胞毒性。为验证细胞凋亡,检测了DNA片段化(通过酶联免疫吸附测定)和半胱天冬酶3/7活性。我们还使用人生长因子抗体阵列研究了多西他赛与奥曲肽联合对前列腺癌细胞分泌的生长因子的影响。结果 多西他赛与奥曲肽联合产生了显著的协同细胞毒性活性和细胞凋亡,且呈剂量和时间依赖性。联合治疗还导致PC-3细胞中干细胞因子和血小板衍生生长因子-AB的分泌,以及DU-145细胞中转化生长因子-β和碱性成纤维细胞生长因子的分泌,与未处理的对照组相比显著减少。结论 生长抑素类似物奥曲肽与多西他赛联合,可能为激素难治性前列腺癌细胞提供一种合理的治疗选择,不仅通过直接抑制细胞增殖,还通过抑制生长因子的分泌。

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