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Evaluation of gene expression of PLEKHS1, AADAC, and CDKN3 as novel genomic markers in gastric carcinoma

Gastric cancer (GC) is considered lethal aggressive cancer. In Egypt, GC has a low incidence but unfortunately, it is mostly diagnosed at an advanced stage with a poor prognosis. Assessment of novel markers that can be used in the early detection of GC is an urgent need. The present study was perfor...

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Autores principales: Abdel-Tawab, Marwa Sayed, Fouad, Hanan, Othman, Asmaa M., Eid, Ragaey A., Mohammed, Marwa Abdeltawab, Hassan, Ahmed, Reyad, Hoda Ramadan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9022821/
https://www.ncbi.nlm.nih.gov/pubmed/35446856
http://dx.doi.org/10.1371/journal.pone.0265184
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author Abdel-Tawab, Marwa Sayed
Fouad, Hanan
Othman, Asmaa M.
Eid, Ragaey A.
Mohammed, Marwa Abdeltawab
Hassan, Ahmed
Reyad, Hoda Ramadan
author_facet Abdel-Tawab, Marwa Sayed
Fouad, Hanan
Othman, Asmaa M.
Eid, Ragaey A.
Mohammed, Marwa Abdeltawab
Hassan, Ahmed
Reyad, Hoda Ramadan
author_sort Abdel-Tawab, Marwa Sayed
collection PubMed
description Gastric cancer (GC) is considered lethal aggressive cancer. In Egypt, GC has a low incidence but unfortunately, it is mostly diagnosed at an advanced stage with a poor prognosis. Assessment of novel markers that can be used in the early detection of GC is an urgent need. The present study was performed to assess the association of the Pleckstrin homology domain-containing S1 (PLEKHS1)، arylacetamide deacetylase (AADAC, and Cyclin-dependent kinase inhibitor 3 (CDKN3) genes with GC and to correlate their gene expression levels with tumor stage, grade, and other clinicopathological features. The current work was performed on forty gastric tissue samples; twenty in Group 1 with GC tissues at different stages, and grades and twenty in Group 2 (control group) with non-tumorous tissue. PLEKHS1, AADAC, and CDKN3 gene expression were assessed by RT-qPCR. AADAC, CDKN3 genes were significantly (p<0.001) upregulated, while PLEKHS1 gene was significantly (p<0.001) downregulated in the GC group than the control group. AADAC gene expression exhibited a high significant (p<0.001) positive correlation with the tumor grades and the tumor stages. A high significant negative correlation between AADAC, and CDKN3 gene expression (r = -.760, p<0.001) was found. The three studied parameters showed high significant sensitivity and specificity in the prediction of the presence of GC. PLEKHS1, AADAC, and CDKN3 gene expressions were suggested to be used as diagnostic and predictive biomarkers of GC, additionally, AADAC may be used as a prognostic marker in these patients for further future confirming studies.
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spelling pubmed-90228212022-04-22 Evaluation of gene expression of PLEKHS1, AADAC, and CDKN3 as novel genomic markers in gastric carcinoma Abdel-Tawab, Marwa Sayed Fouad, Hanan Othman, Asmaa M. Eid, Ragaey A. Mohammed, Marwa Abdeltawab Hassan, Ahmed Reyad, Hoda Ramadan PLoS One Research Article Gastric cancer (GC) is considered lethal aggressive cancer. In Egypt, GC has a low incidence but unfortunately, it is mostly diagnosed at an advanced stage with a poor prognosis. Assessment of novel markers that can be used in the early detection of GC is an urgent need. The present study was performed to assess the association of the Pleckstrin homology domain-containing S1 (PLEKHS1)، arylacetamide deacetylase (AADAC, and Cyclin-dependent kinase inhibitor 3 (CDKN3) genes with GC and to correlate their gene expression levels with tumor stage, grade, and other clinicopathological features. The current work was performed on forty gastric tissue samples; twenty in Group 1 with GC tissues at different stages, and grades and twenty in Group 2 (control group) with non-tumorous tissue. PLEKHS1, AADAC, and CDKN3 gene expression were assessed by RT-qPCR. AADAC, CDKN3 genes were significantly (p<0.001) upregulated, while PLEKHS1 gene was significantly (p<0.001) downregulated in the GC group than the control group. AADAC gene expression exhibited a high significant (p<0.001) positive correlation with the tumor grades and the tumor stages. A high significant negative correlation between AADAC, and CDKN3 gene expression (r = -.760, p<0.001) was found. The three studied parameters showed high significant sensitivity and specificity in the prediction of the presence of GC. PLEKHS1, AADAC, and CDKN3 gene expressions were suggested to be used as diagnostic and predictive biomarkers of GC, additionally, AADAC may be used as a prognostic marker in these patients for further future confirming studies. Public Library of Science 2022-04-21 /pmc/articles/PMC9022821/ /pubmed/35446856 http://dx.doi.org/10.1371/journal.pone.0265184 Text en © 2022 Abdel-Tawab et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Abdel-Tawab, Marwa Sayed
Fouad, Hanan
Othman, Asmaa M.
Eid, Ragaey A.
Mohammed, Marwa Abdeltawab
Hassan, Ahmed
Reyad, Hoda Ramadan
Evaluation of gene expression of PLEKHS1, AADAC, and CDKN3 as novel genomic markers in gastric carcinoma
title Evaluation of gene expression of PLEKHS1, AADAC, and CDKN3 as novel genomic markers in gastric carcinoma
title_full Evaluation of gene expression of PLEKHS1, AADAC, and CDKN3 as novel genomic markers in gastric carcinoma
title_fullStr Evaluation of gene expression of PLEKHS1, AADAC, and CDKN3 as novel genomic markers in gastric carcinoma
title_full_unstemmed Evaluation of gene expression of PLEKHS1, AADAC, and CDKN3 as novel genomic markers in gastric carcinoma
title_short Evaluation of gene expression of PLEKHS1, AADAC, and CDKN3 as novel genomic markers in gastric carcinoma
title_sort evaluation of gene expression of plekhs1, aadac, and cdkn3 as novel genomic markers in gastric carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9022821/
https://www.ncbi.nlm.nih.gov/pubmed/35446856
http://dx.doi.org/10.1371/journal.pone.0265184
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