Aberrant DNA Methylation of FTH-1 and SHOX2 Contributes to Lung Cancer Progression

Background: Lung cancer is the most lethal malignancy in the world due to its poor prognosis. DNA methylation change has been identified as a valuable target for cancer, diagnosis, and prognosis. Ferritin heavy chain 1 (FTH-1) and SHOX homeobox 2 (SHOX2) DNA methylation were investigated in non-smal...

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Main Authors: Salar Tahmasbi, Armin Sadeghi, Habib Zarredar, Milad Asadi, Shahryar Hashemzadeh, Venus Zafari, Hamed Sabbagh-Jadid, Mortaza Raeisi
Format: Article
Language:English
Published: Shiraz University of Medical Sciences 2025-01-01
Series:Middle East Journal of Cancer
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Online Access:https://mejc.sums.ac.ir/article_50081_b04483ac33a6446c19c90f7f48a91f53.pdf
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author Salar Tahmasbi
Armin Sadeghi
Habib Zarredar
Milad Asadi
Shahryar Hashemzadeh
Venus Zafari
Hamed Sabbagh-Jadid
Mortaza Raeisi
author_facet Salar Tahmasbi
Armin Sadeghi
Habib Zarredar
Milad Asadi
Shahryar Hashemzadeh
Venus Zafari
Hamed Sabbagh-Jadid
Mortaza Raeisi
author_sort Salar Tahmasbi
collection DOAJ
description Background: Lung cancer is the most lethal malignancy in the world due to its poor prognosis. DNA methylation change has been identified as a valuable target for cancer, diagnosis, and prognosis. Ferritin heavy chain 1 (FTH-1) and SHOX homeobox 2 (SHOX2) DNA methylation were investigated in non-small cell lung cancer (NSCLC) as novel epigenetic biomarkers.Method: In this case-control study, we initially evaluated the diagnostic value of FTH-1 and SHOX2 DNA methylation, and the Cancer Genome Atlas (TCGA) data on the methylation profile of NSCLC was analyzed. Whole DNA was extracted and bisulfite modification was performed. Then, the methylation status of FTH-1 and SHOX2 was evaluated using quantitative methylation specific polymerase chain reaction (PCR) (qMSP). We used GraphPad Prism version 6.00 program for statistical analysis. Mann-Whitney U test (TCGA-LUNG), paired t-test (internal samples) and receiver operating characteristic (ROC) curve analysis were used to evaluate the statistical differences of DNA methylation between NSCLC tissues samples and adjacent normal specimens (P < 0.05, mean ± SD).Results: TCGA and q-MSP results showed significant FTH-1 hypomethylation and SHOX2 hypermethylation in NSCLC tissues in comparison with margin specimens. Also, FTH-1 and SHOX2 methylation levels were significantly associated with the clinical stage of malignancy. Furthermore, The ROC curve analysis revealed that the area under the curve values for FTH-1 and SHOX2 were determined to be 0.751 and 0.8676, respectively. This indicates the importance of FTH-1 and SHOX2 as diagnostic biomarkers for NSCLC.Conclusion: This study indicates that FTH-1 and SHOX2 methylation could be promising targets for liquid biopsy application of lung cancer.
format Article
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institution Kabale University
issn 2008-6709
2008-6687
language English
publishDate 2025-01-01
publisher Shiraz University of Medical Sciences
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series Middle East Journal of Cancer
spelling doaj-art-175793b8243b4adb8b6e6ebf706202002025-01-13T05:34:02ZengShiraz University of Medical SciencesMiddle East Journal of Cancer2008-67092008-66872025-01-01161596710.30476/mejc.2024.100926.200850081Aberrant DNA Methylation of FTH-1 and SHOX2 Contributes to Lung Cancer ProgressionSalar Tahmasbi0Armin Sadeghi1Habib Zarredar2Milad Asadi3Shahryar Hashemzadeh4Venus Zafari5Hamed Sabbagh-Jadid6Mortaza Raeisi7Tuberculosis and Lung Disease Research Center, Tabriz University of Medical Sciences, Tabriz, IranTuberculosis and Lung Disease Research Center, Tabriz University of Medical Sciences, Tabriz, IranTuberculosis and Lung Disease Research Center, Tabriz University of Medical Sciences, Tabriz, IranDepartment of Basic Oncology, Health Institute, Ege University, Izmir, TurkeyTuberculosis and Lung Disease Research Center, Tabriz University of Medical Sciences, Tabriz, IranDepartment of Basic Oncology, Health Institute, Ege University, Izmir, TurkeyTuberculosis and Lung Disease Research Center, Tabriz University of Medical Sciences, Tabriz, IranHematology and Oncology Research Center, Tabriz University of Medical Sciences, Tabriz, IranBackground: Lung cancer is the most lethal malignancy in the world due to its poor prognosis. DNA methylation change has been identified as a valuable target for cancer, diagnosis, and prognosis. Ferritin heavy chain 1 (FTH-1) and SHOX homeobox 2 (SHOX2) DNA methylation were investigated in non-small cell lung cancer (NSCLC) as novel epigenetic biomarkers.Method: In this case-control study, we initially evaluated the diagnostic value of FTH-1 and SHOX2 DNA methylation, and the Cancer Genome Atlas (TCGA) data on the methylation profile of NSCLC was analyzed. Whole DNA was extracted and bisulfite modification was performed. Then, the methylation status of FTH-1 and SHOX2 was evaluated using quantitative methylation specific polymerase chain reaction (PCR) (qMSP). We used GraphPad Prism version 6.00 program for statistical analysis. Mann-Whitney U test (TCGA-LUNG), paired t-test (internal samples) and receiver operating characteristic (ROC) curve analysis were used to evaluate the statistical differences of DNA methylation between NSCLC tissues samples and adjacent normal specimens (P < 0.05, mean ± SD).Results: TCGA and q-MSP results showed significant FTH-1 hypomethylation and SHOX2 hypermethylation in NSCLC tissues in comparison with margin specimens. Also, FTH-1 and SHOX2 methylation levels were significantly associated with the clinical stage of malignancy. Furthermore, The ROC curve analysis revealed that the area under the curve values for FTH-1 and SHOX2 were determined to be 0.751 and 0.8676, respectively. This indicates the importance of FTH-1 and SHOX2 as diagnostic biomarkers for NSCLC.Conclusion: This study indicates that FTH-1 and SHOX2 methylation could be promising targets for liquid biopsy application of lung cancer.https://mejc.sums.ac.ir/article_50081_b04483ac33a6446c19c90f7f48a91f53.pdfdna methylationepigeneticcarcinomanon-small-cell lung
spellingShingle Salar Tahmasbi
Armin Sadeghi
Habib Zarredar
Milad Asadi
Shahryar Hashemzadeh
Venus Zafari
Hamed Sabbagh-Jadid
Mortaza Raeisi
Aberrant DNA Methylation of FTH-1 and SHOX2 Contributes to Lung Cancer Progression
Middle East Journal of Cancer
dna methylation
epigenetic
carcinoma
non-small-cell lung
title Aberrant DNA Methylation of FTH-1 and SHOX2 Contributes to Lung Cancer Progression
title_full Aberrant DNA Methylation of FTH-1 and SHOX2 Contributes to Lung Cancer Progression
title_fullStr Aberrant DNA Methylation of FTH-1 and SHOX2 Contributes to Lung Cancer Progression
title_full_unstemmed Aberrant DNA Methylation of FTH-1 and SHOX2 Contributes to Lung Cancer Progression
title_short Aberrant DNA Methylation of FTH-1 and SHOX2 Contributes to Lung Cancer Progression
title_sort aberrant dna methylation of fth 1 and shox2 contributes to lung cancer progression
topic dna methylation
epigenetic
carcinoma
non-small-cell lung
url https://mejc.sums.ac.ir/article_50081_b04483ac33a6446c19c90f7f48a91f53.pdf
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