Department of Surgery, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea.
J Breast Cancer. 2011 Dec;14(4):262-8. doi: 10.4048/jbc.2011.14.4.262. Epub 2011 Dec 27.
The expression of Annexin A1 (ANXA1) is known to be reduced in human breast cancer; however, the role of ANXA1 expression in the development of breast cancer remains unclear. In this study, we determined the relationship between the expression features of ANXA1 and the prognostic factors of breast cancer.
Human breast tissues were obtained from patients specimens who had undergone breast surgery or core needle biopsies. The patterns of ANXA1 expression were analyzed by immunohistochemical staining in relation to histopathological diagnosis, clinical characteristics and outcomes.
One hundred eighty-two cases were included and the mean age of the patients was 46.34 ± 11.5 years. A significant loss of ANXA1 expression was noted in both ductal carcinoma in situ (DCIS) and invasive carcinomas compared to normal breast tissues (p<0.001) and benign breast diseases (p<0.001). There was a significant alteration in ANXA1 expression according to hormone receptor status (p<0.001), cancer intrinsic type (p<0.001), and nuclear grade (p=0.004) in invasive cancer. In a univariate analysis, ANXA1 positivity tended to be related with poor breast cancer-related survival (p=0.062); however, the same results was not realized in multivariate results (p=0.406). HER2 overexpression and TNM staging were significantly associated with relapse-free survivals (RFS) in the multivariate analysis (p=0.037, p=0.048, respectively). In particular, in node-positive patients (p=0.048), HER2 overexpressed patients (p=0.013), and non-triple negative breast cancer patients (p=0.002), ANXA1 overexpression was correlated with poor RFS.
Although significant loss of ANXA1 expression was noted in breast cancer including DCIS and invasive carcinoma, in cases of invasive cancer, overexpression of ANXA1 was related to unfavorable prognostic factors. And these results imply that ANXA1 plays dualistic roles and is involved in variable mechanisms related to cancer development and progression.
已知膜联蛋白 A1(ANXA1)在人类乳腺癌中的表达降低;然而,ANXA1 表达在乳腺癌发展中的作用尚不清楚。在这项研究中,我们确定了 ANXA1 表达特征与乳腺癌预后因素之间的关系。
从接受过乳房手术或核心针活检的患者标本中获得人乳腺组织。通过免疫组织化学染色分析 ANXA1 表达模式与组织病理学诊断、临床特征和结果的关系。
共纳入 182 例患者,患者的平均年龄为 46.34±11.5 岁。与正常乳腺组织(p<0.001)和良性乳腺疾病(p<0.001)相比,导管原位癌(DCIS)和浸润性癌中均明显丧失 ANXA1 表达。在浸润性癌中,根据激素受体状态(p<0.001)、癌症固有类型(p<0.001)和核分级(p=0.004),ANXA1 表达发生显著改变。在单因素分析中,ANXA1 阳性与乳腺癌相关生存不良(p=0.062)相关;然而,在多变量分析中,结果相同(p=0.406)。HER2 过表达和 TNM 分期在多变量分析中与无复发生存率(RFS)显著相关(p=0.037,p=0.048)。特别是在淋巴结阳性患者(p=0.048)、HER2 过表达患者(p=0.013)和非三阴性乳腺癌患者(p=0.002)中,ANXA1 过表达与 RFS 不良相关。
尽管在包括 DCIS 和浸润性癌在内的乳腺癌中观察到 ANXA1 表达明显降低,但在浸润性癌中,ANXA1 的过表达与不良的预后因素有关。这些结果表明 ANXA1 发挥双重作用,并参与与癌症发展和进展相关的各种机制。