路洪超, 耿翠芝①, 宋连柱, 王荣茂, 陈 萌, 杨瑞玲①, 周 军①. 乳腺癌组织中BCAR1 p130Cas 蛋白的表达及其临床意义*[J]. 中国肿瘤临床, 2009, 36(1): 29-32. DOI: 10.3969/j.issn.1000-8179.2009.01.009
引用本文: 路洪超, 耿翠芝①, 宋连柱, 王荣茂, 陈 萌, 杨瑞玲①, 周 军①. 乳腺癌组织中BCAR1 p130Cas 蛋白的表达及其临床意义*[J]. 中国肿瘤临床, 2009, 36(1): 29-32. DOI: 10.3969/j.issn.1000-8179.2009.01.009
LU Hongchao1, GENG Cuizhi2, SONG Lianzhu1, WANG Rongmao1, CHEN Meng1, YANG Ruiling2, ZHOU Jun2. The Expression of BCAR 1/p 130Cas Protein in Breast Cancer and Its Significance[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2009, 36(1): 29-32. DOI: 10.3969/j.issn.1000-8179.2009.01.009
Citation: LU Hongchao1, GENG Cuizhi2, SONG Lianzhu1, WANG Rongmao1, CHEN Meng1, YANG Ruiling2, ZHOU Jun2. The Expression of BCAR 1/p 130Cas Protein in Breast Cancer and Its Significance[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2009, 36(1): 29-32. DOI: 10.3969/j.issn.1000-8179.2009.01.009

乳腺癌组织中BCAR1 p130Cas 蛋白的表达及其临床意义*

The Expression of BCAR 1/p 130Cas Protein in Breast Cancer and Its Significance

  • 摘要: 目的:探讨BCAR1/p 130Cas蛋白在乳腺癌组织中的表达及其与乳腺癌内分泌治疗耐药及预后的关系。方法:选择ER阳性且经过规范化内分泌治疗和随访5 年资料完整的乳腺癌患者67例,应用免疫组化方法检测其BCAR1/p 130Cas蛋白表达情况,回顾性分析BCAR1/p 130Cas蛋白表达与乳腺癌的临床生物学特征及预后的关系。结果:在发生局部复发或远位转移的29例患者中,25例呈现BCAR1/p 130Cas蛋白高表达,占86.2% ,无复发转移的38例中,BCAR1/p 130Cas 蛋白高表达仅为21.1% ,两组差异显著(χ2=27.935,P=0.000);乳腺癌组织中BCAR1/p130Cas蛋白表达与高组织学分级(r=0.270,P=0.027)、C-erbB-2 蛋白高表达(r=0.492,P=0.000)以及绝经状况(χ2=13.77,P=0.003)呈现正相关;与肿瘤大小(P=0.548)、病理类型(P=0.177)、淋巴结状况(P=0.720)、TNM分期(P=0.524)无统计学差异(P>0.05)。 结论:BCAR1/p 130Cas蛋白的表达水平与肿瘤的侵袭性显著相关,BCAR1/p 130Cas蛋白的表达水平越高肿瘤的恶性程度越高,所以BCAR1/p 130Cas蛋白高表达患者的复发、转移风险增加;BCAR1/p130Cas蛋白高表达与三苯氧胺治疗耐药密切相关;芳香化酶抑制剂是绝经后ER阳性乳腺癌患者内分泌治疗的最佳选择。BCAR1/p 130Cas蛋白的表达水平和腋淋巴结转移状况、肿瘤大小、病理类型、TNM分期无关。因此认为,BCAR1/p 130Cas蛋白可以作为独立判定乳腺癌预后的一个重要参数,为监测乳腺癌的转移提供了一个有价值的指标,有助于乳腺癌复发转移的诊断及治疗。

     

    Abstract: Objective: To detect the expression of BCAR1/p 130 Cas protein in primary breast cancer and its antiestrogen resistance during endocrine therapy, and to investigate the relationship between expression of the BCAR 1 gene and the prognosis of breast cancer.Methods:A total of 67ER-positive primary breast can -cer patients were randomly recruited between 2000 and 2001. These patients received standardized therapy including endocrine therapy and were followed up for 5 years. We used immunohistochemistry to detect the expression of BCAR1/p 130 Cas protein in the breast cancer samples. We also analyzed the association be-tween BCAR 1/p 130 Cas protein expression and clinicopathologic features including tumor size, pathological type, differentiation degree, menstruation status, lymph node metastasis, TNM staging, and efficacy of tamoxi -fen for endocrine therapy. Results: Of the 67ER-positive breast cancer cases, 29died of disease recurrence or metastasis. The other38patients had no recurrence or metastasis. Of the29patients who died of recur -rence or metastasis, 25cases were BCAR1/p 130 Cas protein positive, accounting for86.2% . Of the 38pa-tients without disease recurrence or metastasis, there were only 8 patients with BCAR 1/p 130 Cas protein ex-pression, accounting for 21.1%. A positive correlation was found between BCAR1/p 130 Cas protein level and relapse-free survival ( χ 2 =27.935 ; P=0.000 ). A positive correlation was found between the expression of BCAR 1/p 130 Cas protein and differentiation degree ( r=0.270 , P=0.027 ). A positive correlation was also found between the expression of BCAR 1/p 130 Cas protein and protein expression of C-erbB-2 (r=0.492 , P=0.000 ) in ER-positive breast cancer tissues. BCAR1/p 130 Cas protein expression was correlated with menstruation status ( χ 2 =13.77, P=0.003 ). No correlation was found between the expression of BCAR1/p 130 Cas protein and tu- mor size (P=0.548 ), pathological type (P=0.177 ), lymph node metastasis ( P=0.720 ) or TNM stage ( P=0.524 ). Conclusion: Breast cancer patients with high BCAR1/p 130 Cas protein expression had higher risk of relapse or metastasis. Overexpression of BCAR 1/p 130 Cas protein is correlated with tamoxifen resistance. Fadrozol is the best choice for endocrine therapy in postmenopausal breast cancer patients with ER-positive tumors. The BCAR 1/p 130 Cas protein may play a role in the progression of breast cancer. Elucidation of this critical pathway will be helpful for the development of new treatment strategies for antiestrogen resistant breast cancer.

     

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