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Relationship between changes in prostate cancer cell proliferation, apoptotic index, and expression of apoptosis-related proteins by neoadjuvant hormonal therapy and duration of such treatment.

机译:新辅助激素治疗的前列腺癌细胞增殖,凋亡指数和凋亡相关蛋白表达的变化与治疗持续时间之间的关系。

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OBJECTIVES: To investigate the relationships between changes in the carcinoma cell proliferation index, apoptotic index (AI), and apoptosis-related factors, including bcl-2 and bax, after different durations of neoadjuvant hormonal therapy (NHT) in prostate cancer tissue. METHODS: Pre- and post-NHT specimens were obtained from 42 patients who had undergone NHT and radical prostatectomy. The patients were divided into two groups according to the duration of NHT: group 1 (3 to 7 months, n = 21) and group 2 (8 to 12 months, n = 21; no randomization). Immunohistochemistry was used to determine the expression of bcl-2 and bax and to determine the proliferation index, and the terminal deoxynucleotidyl transferase-mediated nick end-labeling method was used to assess apoptosis and determine the AI. RESULTS: The median proliferation indexes of groups 1 (1.8%) and 2 (1.6%) were significantly lower than the respective values in the pre-NHT specimens (4.9%, P < 0.01). The median AI of group 1 (2.5%) was greater than in the pre-NHT specimens (1.4%). In addition, the post/pre-NHT AI ratio correlated significantly with the duration of NHT in group 1 (r = 0.58, P < 0.01), but not in group 2. Bax expression increased in a manner parallel to that of the AI. CONCLUSIONS: NHT suppresses prostate cancer cell proliferation for 3 to 12 months. Although the AI was increased during 3 to 7 months of NHT, no significant difference was found between the pre-NHT levels and those after 8 to 12 months. Our results support the current belief that the optimal duration of NHT is longer than 3 months.
机译:目的:研究前列腺癌组织新辅助激素治疗(NHT)持续时间不同后,癌细胞增殖指数,凋亡指数(AI)和凋亡相关因子(包括bcl-2和bax)变化之间的关系。方法:从42例行NHT和根治性前列腺切除术的患者中获得NHT前后的样本。根据NHT的持续时间将患者分为两组:第1组(3至7个月,n = 21)和第2组(8至12个月,n = 21;无随机分组)。免疫组织化学法测定bcl-2和bax的表达并测定增殖指数,末端脱氧核苷酸转移酶介导的缺口末端标记法评估细胞凋亡并确定AI。结果:第1组的中值增殖指数(1.8%)和第2组的中值增殖指数(1.6%)显着低于NHT前的相应值(4.9%,P <0.01)。第一组的中位数AI(2.5%)大于NHT之前的样本(1.4%)。此外,第1组的NHT后AI比率与NHT的持续时间显着相关(r = 0.58,P <0.01),而第2组则不相关。Bax表达以与AI平行的方式增加。结论:NHT可抑制前列腺癌细胞增殖3到12个月。尽管在NHT的3到7个月期间AI升高,但在NHT之前的水平与8到12个月后的水平之间没有发现明显差异。我们的结果支持了目前的观点,即NHT的最佳持续时间超过3个月。

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