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首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >Expression of X-linked inhibitor of apoptosis protein in human prostate cancer specimens with and without neo-adjuvant hormonal therapy.
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Expression of X-linked inhibitor of apoptosis protein in human prostate cancer specimens with and without neo-adjuvant hormonal therapy.

机译:X连锁凋亡抑制蛋白在有或没有新辅助激素治疗的人前列腺癌标本中的表达。

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摘要

PURPOSE: X-linked inhibitor of apoptosis (XIAP) has high affinity and strong inhibitory activity on apoptosis-related caspase-3. The relationships between expression of XIAP and cleaved caspase-3, and response to neo-adjuvant hormonal therapy (NHT) remain elusive. The aim was to investigate whether NHT influences with XIAP expression in prostate cancer patients. In addition, the relationship between XIAP expression and apoptosis in patients who did or did not receive NHT was also investigated. METHODS: Eighty-three patients who had undergone radical prostatectomy were examined retrospectively and divided into NHT group (n = 40) and non-NHT group (n = 43). Immunohistochemistry was used to analyze the expressions of XIAP and cleaved caspase-3. The apoptotic cells reconfirmed the number of terminal deoxynucleotidyl transferase-mediated nick and labeling (TUNEL)-positive cells. RESULTS: In the non-NHT group, the proportion of TUNEL-positive cells correlated with expression of cleaved caspase-3 (r = 0.592, P < 0.001), and the expression of XIAP correlated negatively with that of cleaved caspase-3 and TUNEL-positive cells (r = -0.464, P < 0.001 and r = 0.431, P = 0.002, respectively). The expression of cleaved caspase-3, but not that of XIAP, was higher in NHT group than non-NHT group (P = 0.017). In the NHT group, there was no significant correlation between XIAP expression and cleaved caspase-3 expression or the proportion of TUNEL-positive cells. CONCLUSIONS: NHT did not influence XIAP expression. We speculate that the inhibition of XIAP expression may reinforce the apoptotic effect of NHT and improve the prognosis in patients with prostate cancer.
机译:目的:X连锁凋亡抑制剂(XIAP)对凋亡相关的caspase-3具有高亲和力和较强的抑制活性。 XIAP和裂解的caspase-3的表达与对新辅助激素治疗(NHT)的反应之间的关系仍然难以捉摸。目的是研究NHT是否会影响前列腺癌患者的XIAP表达。另外,还研究了接受或未接受NHT的患者中XIAP表达与细胞凋亡之间的关系。方法:对83例行根治性前列腺切除术的患者进行回顾性检查,将其分为NHT组(n = 40)和非NHT组(n = 43)。免疫组化分析XIAP和裂解的caspase-3的表达。凋亡细胞再次证实了末端脱氧核苷酸转移酶介导的切口和标记(TUNEL)阳性细胞的数量。结果:在非NHT组中,TUNEL阳性细胞比例与裂解的caspase-3表达相关(r = 0.592,P <0.001),而XIAP的表达与裂解的caspase-3和TUNEL呈负相关。阳性细胞(分别为r = -0.464,P <0.001和r = 0.431,P = 0.002)。 NHT组比非NHT组的caspase-3裂解表达高,而XIAP则不高(P = 0.017)。在NHT组中,XIAP表达与切割的caspase-3表达或TUNEL阳性细胞比例之间无显着相关性。结论:NHT不影响XIAP表达。我们推测,XIAP表达的抑制作用可能会增强NHT的凋亡作用,并改善前列腺癌患者的预后。

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