Correlation between the immune checkpoints and EMT genes proposes potential prognostic and therapeutic targets in ESCC

PD-1, PD-L1, CTLA-4, TIM-3, and LAG-3, crucial immune checkpoint molecules in the tumor microenvironment, identify as key targets for cancer immunotherapy. There is a correlation between immune cells and epithelial-mesenchymal transition (EMT)-related genes expression in varies human cancers. In thi...

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Veröffentlicht in:Journal of molecular histology 2021-06, Vol.52 (3), p.597-609
Hauptverfasser: Mahmoudian, Reihaneh Alsadat, Mozhgani, Sahar, Abbaszadegan, Mohammad Reza, Mokhlessi, Leila, Montazer, Mehdi, Gholamin, Mehran
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Sprache:eng
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Zusammenfassung:PD-1, PD-L1, CTLA-4, TIM-3, and LAG-3, crucial immune checkpoint molecules in the tumor microenvironment, identify as key targets for cancer immunotherapy. There is a correlation between immune cells and epithelial-mesenchymal transition (EMT)-related genes expression in varies human cancers. In this study, we aimed to investigate the probable association between expression of immune checkpoints and EMT in esophageal squamous cell carcinoma (ESCC) with clinical treats for providing the new therapeutic targets and prognostic value for the disease. Quantitative real-time PCR was used to investigate the gene expression profile of immune checkpoints ( PD-1 , PD-L1 , CTLA-4 , TIM-3 , and LAG-3 ) and EMT ( TWIST1 and MMP-13 ) genes based on the mRNA expression levels in 51 ESCC tissues. The upregulation of CTLA-4, PD-1, PD-L1, TIM-3 , LAG-3 , MMP-13 , and TWIST1 were observed in 31.37%, 29.41%, 21.56%, 39.21%, 25.49%, 60.78%, and 56.86% of ESCC cases at the mRNA level, respectively. Dysregulation of immune checkpoints was related to lymph node involvement, stage of tumor progression, and depth of tumor invasion ( P  
ISSN:1567-2379
1567-2387
DOI:10.1007/s10735-021-09971-3