{"title":"Specific association of <i>MTHFD1</i> expressions with small cell lung cancer development and chemoradiotherapy outcome.","authors":"Yujia Hao, Ruichun Lu, Ying Guo, Pengtao Bao","doi":"10.15537/smj.2024.45.8.20230990","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>To identify biomarkers that can discriminated small cell lung cancer (SCLC) from non-SCLC (NSCLC), and explore their association with the prognosis of SCLC under chemoradiotherapy.</p><p><strong>Methods: </strong>The GSE40275 dataset was used to identify potential targets in SCLC. There were 196 patients of lung cancer (LC) in cohort 1 of this study. <i>MTHFD1</i> levels in tissues were determined by immunohistochemistry assay in cohort 1. Lung cancer patients who were all underwent local chemoradiotherapy (CRT) were included in cohort 2, and the association of <i>MTHFD1</i> levels with CRT treatment outcome were determined in cohort 2. Cell experiments were used to determine the function of <i>MTHFD1</i> on the radio-sensitivity of SCLC and NSCLC cells.</p><p><strong>Results: </strong>The <i>MTHFD1</i> levels in LC tissues were increased, and could discriminate SCLC from both lung squamous cell carcinoma (LUSC) and lung adenocarcinoma (LUAD). Small cell lung cancer patients with <i>MTHFD1</i> high phenotype had a poorer prognosis after CRT treatment, whereas no significant correlation was found between <i>MTHFD1</i> levels and prognosis in LUSC and LUAD group. Cell experiments demonstrated that overexpression of <i>MTHFD1</i> increases radio-resistance in both SCLC and NSCLC in vitro.</p><p><strong>Conclusion: </strong><i>MTHFD1</i> expressions might be a novel specifically prognostic biomarker for SCLC and the CRT treatment outcome.</p>","PeriodicalId":21453,"journal":{"name":"Saudi Medical Journal","volume":"45 8","pages":"783-790"},"PeriodicalIF":1.7000,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11288495/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Saudi Medical Journal","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.15537/smj.2024.45.8.20230990","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives: To identify biomarkers that can discriminated small cell lung cancer (SCLC) from non-SCLC (NSCLC), and explore their association with the prognosis of SCLC under chemoradiotherapy.
Methods: The GSE40275 dataset was used to identify potential targets in SCLC. There were 196 patients of lung cancer (LC) in cohort 1 of this study. MTHFD1 levels in tissues were determined by immunohistochemistry assay in cohort 1. Lung cancer patients who were all underwent local chemoradiotherapy (CRT) were included in cohort 2, and the association of MTHFD1 levels with CRT treatment outcome were determined in cohort 2. Cell experiments were used to determine the function of MTHFD1 on the radio-sensitivity of SCLC and NSCLC cells.
Results: The MTHFD1 levels in LC tissues were increased, and could discriminate SCLC from both lung squamous cell carcinoma (LUSC) and lung adenocarcinoma (LUAD). Small cell lung cancer patients with MTHFD1 high phenotype had a poorer prognosis after CRT treatment, whereas no significant correlation was found between MTHFD1 levels and prognosis in LUSC and LUAD group. Cell experiments demonstrated that overexpression of MTHFD1 increases radio-resistance in both SCLC and NSCLC in vitro.
Conclusion: MTHFD1 expressions might be a novel specifically prognostic biomarker for SCLC and the CRT treatment outcome.
期刊介绍:
The Saudi Medical Journal is a monthly peer-reviewed medical journal. It is an open access journal, with content released under a Creative Commons attribution-noncommercial license.
The journal publishes original research articles, review articles, Systematic Reviews, Case Reports, Brief Communication, Brief Report, Clinical Note, Clinical Image, Editorials, Book Reviews, Correspondence, and Student Corner.