Journal of Internal Medicine Concepts & Practice ›› 2021, Vol. 16 ›› Issue (02): 103-107.doi: 10.16138/j.1673-6087.2021.02.008

• Original article • Previous Articles     Next Articles

The magnitude and clinical implication of SERPINA1 and FHIT methylation in non-small cell lung cancer based on analysis of TCGA database

WANG Jiahui, LI Ning, SUN Xianwen, LIN Yingni, DING Yongjie, SONG Hejie, LI Qingyun()   

  1. Department of Respiratory and Critical Care Medicine, Institute of Respiratory Disease, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China
  • Received:2020-06-10 Online:2021-04-25 Published:2022-07-26
  • Contact: LI Qingyun E-mail:liqingyun68@homtail.com

Abstract:

Objective To investigate the significance of serine protease inhibitor A1 (SERPINA1) and fragile histidine triad(FHIT) methylation in non-small cell lung cancer(NSCLC) patients based on analysis of TCGA database. Methods The information of SERPINA1/FHIT gene expression, methylation information and associated clinical manifestations were retrieved from TCGA database and analyzed both online and offline. The link between the magnitude of SERPINA1 and FHIT methylation and parameters, such as age, gender, histological-type, smoking history and TNM stage, was probed. Results The expression level of SERPINA1 was higher in tumor tissues other than adjacent non-tumor lung tissues in both lung adenocarcinoma (LUAD) and lung squamous-cell cancer (LUSC) (P<0.05). Hypomethylation of SERPINA1 was mostly observed in LUAD tissue of male patients or individuals with metastasis(P<0.05). The methylation of SERPINA1 and FHIT methylation was not affected by smoking history, nor was it associated with TNM stage or overall survival. Conclusions SERPINA1 and FHIT methylation might play a role in lung cancer. Hypomethylation in SERPINA1 is related with metastasis of LUAD.

Key words: Non-small cell lung cancer, Epigenetic, Methylation, Serine protease inhibitor A1, Fragile histidine triad, Cigarette smoking

CLC Number: