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国家自然科学基金(30801376)

作品数:2 被引量:8H指数:2
相关作者:龚畅姚和瑞欧阳能勇更多>>
相关机构:中山大学孙逸仙纪念医院更多>>
发文基金:国家自然科学基金广东省科技计划工业攻关项目广东省医学科学技术研究基金更多>>
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Ubc9 expression predicts chemoresistance in breast cancer被引量:6
2011年
Ubiquitin-conjugating enzyme 9(Ubc9),the sole conjugating enzyme for sumoylation,regulates protein function and plays an important role in tumorigenesis.Whether Ubc9 is involved in the chemoresistance of breast cancer remains unknown.In this study,we aimed to evaluate the contribution of Ubc9 in the chemoresistance of breast cancer.Immunohistochemistry(IHC) was used to examine the expression level of Ubc9.Chi-square test,Wilcoxon test,and one-way ANOVA were applied to analyze the relationship between Ubc9 expression,clinicopathologic features,and clinical response to neoadjuvant chemotherapy.The significance of variables for survival was analyzed by the Cox proportional hazards model in a multivariate analysis.Kaplan-Meier survival curves were plotted and log-rank test was performed.The proportion of Ubc9-positive cells was higher in invasive ductal carcinoma than in normal breast tissues [(48.48 ± 17.94)% vs.(5.82 ± 2.80)%,P < 0.001].High Ubc9 expression was associated with poor differentiation(χ2 = 6.538,P = 0.038),larger tumor size(χ2 = 4.701,P = 0.030),advanced clinical stage(χ2 = 4.651,P = 0.031),lymph node metastasis(χ2 = 9.913,P = 0.010),basal-like phenotype(χ2 = 8.660,P = 0.034),and poor clinical response to neoadjuvant chemotherapy(χ2 = 11.09,P = 0.001).The expected 6-year cumulative disease-free survival rate was 87.32% in patients with low Ubc9 expression compared to 68.78% in those with high Ubc9 expression(χ2 = 4.289,P = 0.038).These data indicate that high Ubc9 expression correlates with poor response to chemotherapy and poor clinical prognosis.
Shi-Feng ChenChang GongMing LuoHe-Rui YaoYun-Jie ZengFeng-Xi Su
关键词:UBC9单因素方差分析卡方检验
靶向Chk2逆转乳腺癌启动细胞化疗耐药的实验研究被引量:2
2011年
目的探讨化疗压力下,乳腺癌启动细胞DNA损伤修复的能力以及DNA损伤修复机制在乳腺癌启动细胞化疗耐药中的作用。方法获取乳腺癌细胞株MCF-7及其阿霉素耐药株AdrR/MCF-7,球囊培养检测乳腺癌细胞的自我更新功能,流式细胞技术检测CD44+/CD24-细胞和侧群细胞的比例,单细胞凝胶电泳实验检测DNA断裂程度。结果 AdrR/MCF-7的球囊形成率高于MCF-7([8.71±0.71)%vs(3.94±1.90)%,P<0.05];AdrR/MCF-7中高表达CD44+/CD24-([59.27±4.86)%vs(1.86±0.60)%,P<0.001],并含有更高比例的侧群细胞([8.43±1.82)%vs(0.20±0.10)%,P<0.01];AdrR/MCF-7比MCF-7能更加迅速地修复阿霉素引起的DNA损伤,拖尾消失(28.33±21.60vs315.00±24.54),且伴有Chk2的异常激活。干预Chk2的激活可以降低乳腺癌启动细胞的DNA损伤修复能力,凋亡细胞比例由(4.86±0.89)%增加至(19.17±0.70)%。结论乳腺癌启动细胞的化疗耐药性与DNA损伤修复能力增强有关,该功能与Chk2的异常激活相关。
欧阳能勇龚畅姚和瑞
关键词:乳腺癌DNA损伤DNA修复化疗耐药CHK2
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