高迁移率A2组增高与非小细胞肺癌淋巴结转移及预后相关。

IF 1.9
Xiangjun Guo, Jiaxin Shi, Yan Wen, Mengmeng Li, Qin Li, Xiaomei Li, Jiashu Li
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引用次数: 12

摘要

背景:高迁移率组A2 (HMGA2)已被研究与肿瘤发生相关;然而,HMGA2在非小细胞肺癌(NSCLC)中的表达模式和临床意义尚不清楚。本研究的目的是检测HMGA2的表达,并分析其与非小细胞肺癌的临床病理特征和患者生存的关系。方法:采用Western blot和免疫组化方法检测HMGA2在NSCLC细胞和组织中的表达水平。采用Kaplan-Meier法计算HMGA2表达与NSCLC患者生存的关系,采用多元回归分析确定危险因素的评价。结果:NSCLC组织中HMGA2表达水平高于正常组织(p< 0.05),且HMGA2表达水平与NSCLC分化不良(p< 0.05)、淋巴结转移(p< 0.05)、临床分期(p< 0.05)相关。此外,Western blot也证实了HMGA2在NSCLC细胞中的表达升高。HMGA2表达升高与NSCLC患者生存率降低相关(p< 0.05)。结论:HMGA2在非小细胞肺癌组织和细胞中高表达,其过表达与非小细胞肺癌的低分化程度、淋巴结转移、临床分期较晚、生存时间较短有关,可作为非小细胞肺癌的潜在分子标志物和预后指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Increased high-mobility group A2 correlates with lymph node metastasis and prognosis of non-small cell lung cancer.

Background: High-mobility group A2 (HMGA2) has been investigated to be associated with tumorigenesis; however, the expression pattern and clinical significance of HMGA2 in non-small cell lung cancer (NSCLC) remains poorly understood. The purpose of this study is to examine the expression of HMGA2 and to analyze its relationships with respect to clinico-pathological features and patient survival in NSCLC.

Methods: The expression level of HMGA2 was examined by Western blot and immunohistochemistry in NSCLC cells and tissues. The relationship between HMGA2 expression and survival of NSCLC patients was calculated by a Kaplan-Meier method and the evaluation of risk factor was determined by the multiple regression analysis.

Results: NSCLC tissues exhibited a higher expression level of HMGA2 compared to normal tissues (p< 0.05) and the expression level of HMGA2 was significantly associated with poor differentiation of NSCLC (p< 0.05), lymph node metastasis (p< 0.05) and advanced clinical stage (p< 0.05). Besides, HMGA2 was also confirmed to be elevated in NSCLC cells by Western blot. Moreover, increased expression of HMGA2 correlated with decreased survival of NSCLC patients (p< 0.05).

Conclusions: HMGA2 was highly expressed in NSCLC tissues and cells and its overexpression was correlated with low-grade differentiation, lymph node metastasis, advanced clinical stage and poor survival time of NSCLC, which suggested that it could serve as a potential molecular marker and prognostic index for NSCLC.

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