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TPX2促进非小细胞肺癌转移并作为预后不良的标志物。

TPX2 Promotes Metastasis and Serves as a Marker of Poor Prognosis in Non-Small Cell Lung Cancer.

作者信息

Zhou Fang, Wang Meng, Aibaidula Mijiti, Zhang Zhiguo, Aihemaiti Abudusaimaiti, Aili Rezhake, Chen Hao, Dong Shuangfeng, Wei Wei, Maimaitiaili Abulizi

机构信息

Department of Thoracic Surgery, Tianjin Chest Hospital, Tianjin, China (mainland).

Department of Cardiothoracic Surgery, People's Hospital of Hetian, Hetian, Xinjiang, China (mainland).

出版信息

Med Sci Monit. 2020 Aug 4;26:e925147. doi: 10.12659/MSM.925147.

Abstract

BACKGROUND Metastasis contributes to the high mortality rate of non-small cell lung cancer (NSCLC), and gaining a better understanding of its metastatic mechanisms would aid in initiating effective clinical treatment. MATERIAL AND METHODS In this study, bioinformatics analyses of the GEO database and TCGA-LUAD were first used to identify the key node gene regulating NSCLC malignant progression. Further in vitro experiments, including wound healing assay, invasion assay, Western blot assay, and luciferase report assay, were used to clarify the functions and mechanism of TPX2 in NSCLC. RESULTS Results of the TCGA analysis showed that TPX2 was significantly positively correlated with tumor metastasis and growth and the clinical stage of NSCLC. In addition, high levels of TPX2 significantly indicated a poor survival rate. In vitro experimental results also revealed that the upregulation of TPX2 significantly promoted NSCLC cell migration and invasion and could affect cell replasticity. Further results indicated that TPX2 significantly activated the epithelial-mesenchymal transition process and promoted the expression and activities of matrix metalloproteinase (MMP)2 and MMP9. CONCLUSIONS This study demonstrated that TPX2 promotes the metastasis and malignant progression of NSCLC and could thus serve as a marker of poor prognosis in NSCLC.

摘要

背景 转移导致非小细胞肺癌(NSCLC)的高死亡率,更好地了解其转移机制将有助于开展有效的临床治疗。材料与方法 在本研究中,首先对GEO数据库和TCGA-LUAD进行生物信息学分析,以鉴定调控NSCLC恶性进展的关键节点基因。进一步的体外实验,包括伤口愈合试验、侵袭试验、蛋白质免疫印迹试验和荧光素酶报告试验,用于阐明TPX2在NSCLC中的功能和机制。结果 TCGA分析结果显示,TPX2与NSCLC的肿瘤转移、生长及临床分期显著正相关。此外,TPX2高表达显著提示生存率较低。体外实验结果还显示,TPX2上调显著促进NSCLC细胞迁移和侵袭,并可影响细胞可塑性。进一步结果表明,TPX2显著激活上皮-间质转化过程,并促进基质金属蛋白酶(MMP)2和MMP9的表达及活性。结论 本研究表明,TPX2促进NSCLC的转移和恶性进展,因此可作为NSCLC预后不良的标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f968/7427348/187d58e124ca/medscimonit-26-e925147-g001.jpg

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