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转移相关蛋白 2(MTA2)的表达可能预测非小细胞肺癌的增殖。

Expression of metastasis-associated protein 2 (MTA2) might predict proliferation in non-small cell lung cancer.

机构信息

Department of Pathology, the First Affiliated Hospital and College of Basic Medical Sciences of China Medical University, Shenyang, 110001, China.

出版信息

Target Oncol. 2012 Jun;7(2):135-43. doi: 10.1007/s11523-012-0215-z. Epub 2012 May 15.

Abstract

Metastatic tumor antigen 2 (MTA2) is a member of the MTA family that is closely associated with tumor progression and metastasis. In this study, the expression profile of MTA2 in 223 cases of non-small cell lung cancer (NSCLC) tissues and two lung cancer cell lines was investigated. Interestingly, we found MTA2, which was believed to have nuclear distribution only, was distributed in both nucleus and cytoplasm in normal and cancer cells. Nuclear MTA2 expression was detected in 148 cases of NSCLC (66.4%), and was correlated with advanced TNM stages (p=0.023), tumor size (p=0.036), and lymph node metastasis (p=0.004). Besides, the Ki-67 proliferation index was significantly higher in nuclear MTA2-positive tumors than in nuclear MTA2-negative tumors (r=0.538, p=0.006). However, there was no significant difference in cytoplasmic MTA2 status by age, gender, tumor stage, histology, grade, lymph node metastasis, and Ki-67 proliferation index. Univariate analysis revealed nuclear MTA2 expression was correlated with poor overall survival (p=0.035), whereas there was a nonsignificant trend in the same direction for cytoplasmic MTA2 (p=0.134). Multivariate Cox regression analysis revealed the overexpression of nuclear and cytoplasmic MTA2 not to be independent factors predictive of poor disease outcome. Our data suggested that MTA2 might play roles in both the nucleus and cytoplasm in the progression of NSCLC.

摘要

转移性肿瘤抗原 2(MTA2)是 MTA 家族的一员,与肿瘤的进展和转移密切相关。在本研究中,我们研究了 223 例非小细胞肺癌(NSCLC)组织和两种肺癌细胞系中 MTA2 的表达谱。有趣的是,我们发现原本被认为只有核分布的 MTA2,在正常和癌细胞中都分布在核和细胞质中。在 148 例 NSCLC 中检测到核 MTA2 表达(66.4%),并且与晚期 TNM 分期(p=0.023)、肿瘤大小(p=0.036)和淋巴结转移(p=0.004)相关。此外,核 MTA2 阳性肿瘤的 Ki-67 增殖指数明显高于核 MTA2 阴性肿瘤(r=0.538,p=0.006)。然而,核 MTA2 状态与年龄、性别、肿瘤分期、组织学、分级、淋巴结转移和 Ki-67 增殖指数之间没有显著差异。单因素分析显示,核 MTA2 表达与总生存期不良相关(p=0.035),而细胞质 MTA2 则呈相同方向的非显著性趋势(p=0.134)。多因素 Cox 回归分析显示,核和细胞质 MTA2 的过表达不是疾病预后不良的独立预测因素。我们的数据表明,MTA2 可能在 NSCLC 的进展中在核和细胞质中发挥作用。

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