Zhao Jing, Liu Caigang, Zhao Zuowei
Gastrointestinal Tumor Pathology Laboratory of Cancer Institute, the First Hospital of China Medical University, Shenyang, China, 110001.
Tumour Biol. 2014 May;35(5):4813-9. doi: 10.1007/s13277-014-1632-7. Epub 2014 Jan 16.
The aim of this study is to explore the expression of BAF250a protein in breast cancer and its association with the clinical and pathological characteristics and prognosis of breast cancer. The expression status of BAF250a protein was detected by Western blot analysis and immunohistochemical staining. The relationship between BAF250a proteins and clinicopathological parameters in 496 breast cancer specimens was analyzed. Western blot analysis showed that BAF250a protein had a lower expression in breast cancer specimens than in matched normal breast tissue (104.38 ± 11.65 vs. 55.94 ± 10.27; P = 0.004, t test). Among the 496 enrolled breast cancer patients, BAF250a protein expression was absent in 324 (65.3 %). Universal and multiple analyses indicated that BAF250a protein expression loss was significantly related to histological grade, metastatic nodes, tumor node metastasis (TNM) stage, and the expression of estrogen receptor (ER), progesterone receptor (PR), c-erbB-2, and p53 (all P < 0.05). For TNM stage, rank correlation coefficients were 0.199 and 0.191, respectively, (P < 0.05), but BAF250a protein deletion had either a positive or a negative correlation with ER, PR, c-erbB-2, and p53 protein expression (correlation coefficients were 0.231, 0.207, -0.098, -0.128; P < 0.05). Analysis of survival rates showed that the patients with BAF250a protein expression attained a significantly better postoperative disease-specific survival than those with BAF250a protein deletion (88.4 vs. 79.0%; P = 0.003). In the Cox regression test, BAF250a protein deletion was detected as an independent prognostic factor (P = 0.014). BAF250a protein might be a new potential target for breast cancer treatment.
本研究旨在探讨BAF250a蛋白在乳腺癌中的表达及其与乳腺癌临床病理特征和预后的关系。通过蛋白质免疫印迹分析和免疫组织化学染色检测BAF250a蛋白的表达状态。分析496例乳腺癌标本中BAF250a蛋白与临床病理参数之间的关系。蛋白质免疫印迹分析显示,BAF250a蛋白在乳腺癌标本中的表达低于配对的正常乳腺组织(104.38±11.65 vs. 55.94±10.27;P = 0.004,t检验)。在496例纳入研究的乳腺癌患者中,324例(65.3%)BAF250a蛋白表达缺失。综合及多因素分析表明,BAF250a蛋白表达缺失与组织学分级、转移淋巴结、肿瘤-淋巴结-转移(TNM)分期以及雌激素受体(ER)、孕激素受体(PR)、c-erbB-2和p53的表达均显著相关(均P < 0.05)。对于TNM分期,等级相关系数分别为0.199和0.191(P < 0.05),但BAF250a蛋白缺失与ER、PR、c-erbB-2和p53蛋白表达呈正相关或负相关(相关系数分别为0.231、0.207、-0.098、-0.128;P < 0.05)。生存率分析显示,BAF250a蛋白表达阳性的患者术后疾病特异性生存率显著高于BAF250a蛋白缺失的患者(88.4% vs. 79.0%;P = 0.003)。在Cox回归检验中,BAF250a蛋白缺失被检测为独立的预后因素(P = 0.014)。BAF250a蛋白可能是乳腺癌治疗的一个新的潜在靶点。