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整合素α3表达降低作为肺腺癌患者预后不良的一个因素。

Reduced integrin alpha3 expression as a factor of poor prognosis of patients with adenocarcinoma of the lung.

作者信息

Adachi M, Taki T, Huang C, Higashiyama M, Doi O, Tsuji T, Miyake M

机构信息

Department of Thoracic Surgery, Kitano Hospital, Tazuke Kofukai Medical Research Institute, Osaka, Japan.

出版信息

J Clin Oncol. 1998 Mar;16(3):1060-7. doi: 10.1200/JCO.1998.16.3.1060.

Abstract

PURPOSE

We investigated the possible association between integrin alpha3 and motility-related protein (MRP-1), cluster of differentiation antigen 9 (CD9) gene expression in non-small-cell lung cancer (NSCLC) and evaluated the prognostic significance of integrin alpha3 expression.

PATIENTS AND METHODS

We performed a retrospective study of integrin alpha3 and MRP-1/CD9 expression in resected tumor tissues from 151 NSCLC patients using quantitative reverse-transcriptase polymerase chain reaction (RT-PCR) and immunohistochemistry.

RESULTS

The ratio of integrin alpha3/beta-actin expression ranged from 0 to 5.87 (mean was 0.80; median, 0.70). Using the cutoff value of 0.7, there were 78 (52%) integrin alpha3-positive tumors and 73 (48%) tumors with reduced integrin alpha3 expression. The immunohistochemical results agreed well with those of the RT-PCR assays, and 88% had no discrepancy. In case of discrepancy, the results of RT-PCR were used in specimen classification. Integrin alpha3 gene expression was independent from MRP-1/CD9 gene expression. No significant association was found between integrin alpha3 expression and the patients' clinical characteristics. The overall survival rate of patients with integrin alpha3-positive NSCLCs was only slightly better than that of individuals whose tumors had reduced integrin alpha3 expression (55.9% v 47.1%; P = .085). By comparison, the overall survival rate of patients with integrin alpha3-positive adenocarcinomas was strikingly greater than in those whose tumors had reduced gene expression (54.4% v 35.2%; P = .004). Multivariate analysis with the Cox regression model of NSCLC and adenocarcinoma indicated that integrin alpha3 expression correlated better (P = .0188 and P = .0008, respectively) with the overall survival rate than other variables, except lymph node status.

CONCLUSION

No significant association was found between integrin alpha3 and MRP-1/CD9 gene expression in lung cancer. However, reduced integrin alpha3 expression is a poor prognosis factor in patients with adenocarcinomas.

摘要

目的

我们研究了整合素α3与运动相关蛋白(MRP-1)、分化抗原簇9(CD9)基因表达在非小细胞肺癌(NSCLC)中的可能关联,并评估了整合素α3表达的预后意义。

患者与方法

我们对151例NSCLC患者手术切除肿瘤组织中的整合素α3和MRP-1/CD9表达进行了回顾性研究,采用定量逆转录聚合酶链反应(RT-PCR)和免疫组织化学方法。

结果

整合素α3/β-肌动蛋白表达比值范围为0至5.87(平均值为0.80;中位数为0.70)。采用0.7的临界值,有78例(52%)整合素α3阳性肿瘤和73例(48%)整合素α3表达降低的肿瘤。免疫组织化学结果与RT-PCR检测结果吻合良好,88%无差异。出现差异时,标本分类采用RT-PCR结果。整合素α3基因表达与MRP-1/CD9基因表达无关。整合素α3表达与患者临床特征之间未发现显著关联。整合素α3阳性NSCLC患者的总生存率仅略高于整合素α3表达降低的患者(55.9%对47.1%;P = 0.085)。相比之下,整合素α3阳性腺癌患者的总生存率显著高于基因表达降低的患者(54.4%对35.2%;P = 0.004)。对NSCLC和腺癌采用Cox回归模型进行多变量分析表明,整合素α3表达与总生存率的相关性优于其他变量(分别为P = 0.0188和P = 0.0008),淋巴结状态除外。

结论

肺癌中整合素α3与MRP-1/CD9基因表达之间未发现显著关联。然而,整合素α3表达降低是腺癌患者预后不良的因素。

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