Evaluation of TET Family Gene Expression and 5-Hydroxymethylcytosine as Potential Epigenetic Markers in Non-small Cell Lung Cancer

DNA methylation is the most studied epigenetic modification in cancer. Ten-eleven translocation enzymes (TET) catalyze the oxidation of 5-methylcytosine (5-mC) to 5-hydroxymethylcytosine (5-hmC) in the DNA. In the current research, we aimed to evaluate the role of 5-hmC and TET enzymes in non-small...

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Veröffentlicht in:In vivo (Athens) 2023-01, Vol.37 (1), p.445-453
Hauptverfasser: Alrehaili, Amani A, Gharib, Amal F, Alghamdi, Saleh Ali, Alhazmi, Ayman, Al-Shehri, Saad S, Hagag, Howaida M, Alsaeedi, Fouzeyyah Ali, Alhuthali, Hayaa M, Raafat, Nermin, Etewa, Rasha L, Elsawy, Wael H
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Sprache:eng
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Zusammenfassung:DNA methylation is the most studied epigenetic modification in cancer. Ten-eleven translocation enzymes (TET) catalyze the oxidation of 5-methylcytosine (5-mC) to 5-hydroxymethylcytosine (5-hmC) in the DNA. In the current research, we aimed to evaluate the role of 5-hmC and TET enzymes in non-small cell lung cancer (NSCLC) patients and their possible association with outcomes. ELISA was used to measure the 5-hmC levels in genomic DNA and qRT-PCR was used to evaluate TET1, TET2, and TET3 mRNAs expression levels in NSCLC tissues and their paired normal controls. The levels of 5-hmC were significantly lower in NSCLC tissues than in normal tissues, with a mean ±SD of 0.28±0.37 vs. 1.84±0.58, respectively (t=22.77, p
ISSN:0258-851X
1791-7549
DOI:10.21873/invivo.13098