TY - JOUR ID - 253283 TI - GPX2 and BMP4 as Significant Molecular Alterations in The Lung Adenocarcinoma Progression: Integrated Bioinformatics Analysis JO - Cell Journal (Yakhteh) JA - CELLJ LA - en SN - 2228-5806 AU - Derakhshan Nazari, Mohammad Hossein AU - Askari Dastjerdi, Rana AU - Ghaedi Talkhouncheh, Parnian AU - Bereimipour, Ahmad AU - Mollasalehi, Hamidreza AU - Mahshad, Amir Ali AU - Razi, Ali AU - Nazari, Mohammad Hossein AU - Ebrahimi Sadrabadi, Amin AU - Taleahmad, Sara AD - Department of Microbiology and Microbial Biotechnology, Faculty of Life Science and Biotechnology, Shahid Beheshti University, Tehran, Iran AD - Department of Cell and Molecular Biology, Faculty of Life Science and Biotechnology, Shahid Beheshti University, Tehran, Iran AD - Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran AD - Biophysics Department, Science Faculty, York University, Toronto, Canada AD - V. Zelman Institute for Medicine and Psychology, Novosibirsk State University, Novosibirsk, Russia Y1 - 2022 PY - 2022 VL - 24 IS - 6 SP - 302 EP - 308 KW - glutathione peroxidase KW - In silico KW - Microarray KW - NSCLC KW - TGF-β Signaling DO - 10.22074/cellj.2022.7930 N2 - Objective: Non-small cell lung adenocarcinoma (NSCLC) is the most common type of lung cancer, which is considered as the most lethal and prevalent cancer worldwide. Recently, molecular changes have been implicated to play a significant role in the cancer progression. Despite of numerous studies, the molecular mechanism of NSCLC pathogenesis in each sub-stage remains unclear. Studying these molecular alterations gives us a chance to design successful therapeutic plans which is aimed in this research.Materials and Methods: In this bioinformatics study, we compared the expression profile of 7 minor stages of NSCLCadenocarcinoma, including GSE41271, GSE42127, and GSE75037, to clarify the relation of molecular alterations and tumorigenesis. At first, 99 common differentially expressed genes (DEG) were obtained. Then, functional enrichment analysis and protein-protein interaction (PPI) network construction were performed to uncover the association of significant cellular and molecular changes. Finally, gene expression profile interactive analysis (GEPIA) was employed to validate the results by RNA-seq expression data.Results: Primary analysis showed that BMP4 was downregulated through the tumor progression to the stage IB andGPX2 was upregulated in the course of final tumor development to the stage IV and distant metastasis. Functional enrichment analysis indicated that BMP4 in the TGF-β signaling pathway and GPX2 in the glutathione metabolism pathway may be the key genes for NSCLC adenocarcinoma progression. GEPIA analysis revealed a correlation between BMP4 downregulation and GPX2 upregulation and lung adenocarcinoma (LUAD) progression and lower survival chances in LUAD patients which confirm microarray data.Conclusion: Taken together, we suggested GPX2 as an oncogene by inhibiting apoptosis, promoting EMT and increasing glucose uptake in the final stages and BMP4 as a tumor suppressor via inducing apoptosis and arresting cell cycle in the early stages through lung adenocarcinoma (ADC) development to make them candidate genes to further cancer therapy investigations. UR - https://www.celljournal.org/article_253283.html L1 - https://www.celljournal.org/article_253283_d7f7e1adb03c0f7aeb1ef8aede725c30.pdf ER -