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TRIM28,一种预测早期非小细胞肺癌转移和生存的新型分子标志物。

TRIM28, a new molecular marker predicting metastasis and survival in early-stage non-small cell lung cancer.

机构信息

Department of Immunology, Basic Medical Institute, Chengde Medical College, Chengde, Hebei Province, 067000, China.

出版信息

Cancer Epidemiol. 2013 Feb;37(1):71-8. doi: 10.1016/j.canep.2012.08.005. Epub 2012 Sep 7.

Abstract

TRIM28 is a universal corepressor for Kruppel-associated box zinc finger proteins. In this study, we demonstrated the expression of TRIM28 gene was significantly higher in cancerous tissues than in noncancerous tissues (P < 0.001). TRIM28 knockdown resulted in a decrease in cell proliferation in liquid media as well as in soft agar. The proliferation rate was impaired and the cell cycle progression was inhibited after knockdown of TRIM28 in non-small cell lung cancer cell lines PAa and SK-MES-1. We used real-time polymerase chain reaction to detect circulating cancer cells in 138 non-small cell lung cancer patients. The overall positive detection rate was 30.4% (42 of 138) in peripheral blood of NSCLC patients and was 29.9% (29 of 97) in early-stage patients. In a 70-month follow-up study, 20 of 29 patients (69.0%) in TRIM28 positive group had recurrence and/or metastasis, significantly higher (P = 0.004) than in the TRIM28 negative group (25 of 68, 36.8%). In addition, non-small cell lung cancer patients whose circulating cancer cells expressed TRIM28 suffered shorter tumor-specific survival compared with those with absent TRIM28 expression (P < 0.001). Results of our study showed that TRIM28 provides a survival advantage to lung cancer cells and may be a new marker to predict metastasis and prognosis in early-stage non-small cell lung cancer patients.

摘要

TRIM28 是一种普遍的 Kruppel 相关盒锌指蛋白的核心抑制剂。在这项研究中,我们证明了 TRIM28 基因在癌组织中的表达明显高于非癌组织(P<0.001)。TRIM28 敲低导致液体培养基和软琼脂中的细胞增殖减少。非小细胞肺癌细胞系 PAa 和 SK-MES-1 中 TRIM28 敲低后,增殖率受损,细胞周期进程受到抑制。我们使用实时聚合酶链反应检测了 138 例非小细胞肺癌患者的循环癌细胞。在非小细胞肺癌患者的外周血中,总体阳性检出率为 30.4%(42/138),早期患者为 29.9%(29/97)。在 70 个月的随访研究中,TRIM28 阳性组的 29 例患者中有 20 例(69.0%)出现复发和/或转移,明显高于 TRIM28 阴性组(25/68,36.8%)(P=0.004)。此外,表达 TRIM28 的循环癌细胞的非小细胞肺癌患者的肿瘤特异性生存率明显低于不表达 TRIM28 的患者(P<0.001)。我们的研究结果表明,TRIM28 为肺癌细胞提供了生存优势,可能是预测早期非小细胞肺癌患者转移和预后的新标志物。

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