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Expression of DNA Damage Response Molecules PARP1 γH2AX BRCA1 and BRCA2 Predicts Poor Survival of Breast Carcinoma Patients

机译:DNA损伤反应分子PARP1γH2AXBRCA1和BRCA2的表达可预测乳腺癌患者的不良生存

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摘要

BACKGROUND: Poly(ADP-ribose) polymerase 1 (PARP1), γH2AX, BRCA1, and BRCA2 are conventional molecular indicators of DNA damage in cells and are often overexpressed in various cancers. In this study, we aimed, using immunohistochemical detection, whether the co-expression of PARP1, γH2AX, BRCA1, and BRCA2 in breast carcinoma (BCA) tissue can provide more reliable prediction of survival of BCA patients. MATERIALS AND METHODS: We investigated immunohistochemical expression and prognostic significance of the expression of PARP1, γH2AX, BRCA1, and BRCA2 in 192 cases of BCAs. RESULTS: The expression of these four molecules predicted earlier distant metastatic relapse, shorter overall survival (OS), and relapse-free survival (RFS) by univariate analysis. Multivariate analysis revealed the expression of PARP1, γH2AX, and BRCA2 as independent poor prognostic indicators of OS and RFS. In addition, the combined expressional pattern of BRCA1, BRCA2, PARP1, and γH2AX (CSbbph) was an additional independent prognostic predictor for OS (P < .001) and RFS (P < .001). The 10-year OS rate was 95% in the CSbbph-low (CSbbph scores 0 and 1) subgroup, but that was only 35% in the CSbbph-high (CSbbph score 4) subgroup. CONCLUSION: This study has demonstrated that the individual and combined expression patterns of PARP1, γH2AX, BRCA1, and BRCA2 could be helpful in determining an accurate prognosis for BCA patients and for the selection of BCA patients who could potentially benefit from anti-PARP1 therapy with a combination of genotoxic chemotherapeutic agents.
机译:背景:聚(ADP-核糖)聚合酶1(PARP1),γH2AX,BRCA1和BRCA2是细胞DNA损伤的常规分子指示剂,在各种癌症中通常过表达。在这项研究中,我们旨在通过免疫组织化学检测来确定乳腺癌(BCA)组织中PARP1,γH2AX,BRCA1和BRCA2的共表达能否为BCA患者的生存提供更可靠的预测。材料与方法:我们调查了192例BCA患者的免疫组化表达和PARP1,γH2AX,BRCA1和BRCA2表达的预后意义。结果:这四种分子的表达通过单因素分析预测较早的远处转移复发,较短的总生存期(OS)和无复发生存期(RFS)。多因素分析显示,PARP1,γH2AX和BRCA2的表达是OS和RFS的独立不良预后指标。此外,BRCA1,BRCA2,PARP1和γH2AX(CSbbph)的组合表达模式是OS(P <.001)和RFS(P <.001)的另一个独立的预后指标。 CSbbph低(CSbbph得分为0和1)子组的10年OS率为95%,而CSbbph高(CSbbph得分为4)子组的10年OS率仅为35%。结论:这项研究表明,PARP1,γH2AX,BRCA1和BRCA2的单独和联合表达模式可能有助于确定BCA患者的准确预后以及选择可能受益于抗PARP1疗法的BCA患者。遗传毒性化学治疗剂的组合。

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