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首页> 外文期刊>American Journal of Cancer Research >BCL6 is a negative prognostic factor and exhibits pro-oncogenic activity in ovarian cancer
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BCL6 is a negative prognostic factor and exhibits pro-oncogenic activity in ovarian cancer

机译:BCL6是阴性预后因子,在卵巢癌中表现出促癌活性

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Background: Dysregulation of BCL6 plays critical oncogenic roles and facilitates tumorigenesis in various malignancies. However, whether the aberrant expression of BCL6 in ovarian carcinoma is associated with malignancy, metastasis or prognosis remains unknown. Our study aimed to investigate the expression of BCL6 in ovarian carcinoma and its possible correlation with clinicopathological features as well as patient survival to reveal its biological effects in ovarian tumor progression. Methods: Immunochemistry analysis was performed in 105 cases of ovarian carcinoma covering the histological types of serous, endometrioid and clear cell. Spearman analysis was used to calculate the correlation between pathological parameters and the expression of BCL6. Kaplan–Meier method and Cox proportional hazards analysis were used to analyze the disease-specific survival (DSS) and disease-free survival (DFS). We also assessed whether overexpression and knockdown of BCL6 influence in vitro cell proliferation, cell cycle progression, as well as tumor cell invasion and migration. Results: The expression of BCL6 was higher in all three major kinds of ovarian cancer in comparison with paratumorous epithelium. BCL6 expression was tightly correlated with FIGO staging, lymph node metastasis and recurrence. Higher expression of BCL6 led to a significantly poorer DSS and DFS and multivariate analysis revealed that BCL6 was an independent risk factor of DSS and DFS. Enforced overexpression of BCL6 in ovarian tumor cells stimulated proliferation by inducing G1–S transition, and promoted tumor cell invasion and migration. Conversely, RNA interference–mediated silencing BCL6 expression inhibited proliferation by altered cell cycle progression and reduced the ability of the cells to migrate, and invade the extracellular matrix in culture. Conclusions: Our study suggests that the inappropriate activation of BCL6 predicts poor prognosis and promotes tumor progression in ovarian carcinoma. Targeting BCL6 could be a novel therapeutic choice for treating ovarian carcinoma patients.
机译:背景:BCL6的失调起着重要的致癌作用,并促进各种恶性肿瘤的发生。然而,卵巢癌中BCL6的异常表达是否与恶性,转移或预后有关仍是未知的。我们的研究旨在调查BCL6在卵巢癌中的表达及其与临床病理特征以及患者生存率的可能关系,以揭示其在卵巢肿瘤进展中的生物学作用。方法:对105例卵巢癌进行免疫化学分析,包括浆液性,子宫内膜样和透明细胞的组织学类型。 Spearman分析用于计算病理参数与BCL6表达之间的相关性。 Kaplan–Meier方法和Cox比例风险分析用于分析特定疾病生存期(DSS)和无疾病生存期(DFS)。我们还评估了BCL6的过表达和敲低是否影响体外细胞增殖,细胞周期进程以及肿瘤细胞的侵袭和迁移。结果:与癌旁上皮相比,三种主要卵巢癌中BCL6的表达均较高。 BCL6表达与FIGO分期,淋巴结转移和复发密切相关。 BCL6的较高表达导致DSS和DFS明显较差,多变量分析表明BCL6是DSS和DFS的独立危险因素。卵巢肿瘤细胞中BCL6的过度表达通过诱导G1–S过渡来刺激增殖,并促进肿瘤细胞的侵袭和迁移。相反,RNA干扰介导的沉默BCL6表达通过改变细胞周期进程抑制增殖,并降低细胞迁移和侵袭培养中细胞外基质的能力。结论:我们的研究表明,不适当激活BCL6可以预示不良预后并促进卵巢癌的肿瘤进展。靶向BCL6可能是治疗卵巢癌患者的新治疗选择。

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