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mRNA Expression of SLC5A5 and SLC2A Family Genes in Papillary Thyroid Cancer: An Analysis of The Cancer Genome Atlas

PURPOSE: The present study investigated the dynamics and prognostic role of messenger RNA (mRNA) expression responsible for (18)F-fluorodeoxyglucose (FDG) uptake in FDG positron emission tomography (PET) and radioactive iodine ((131)I) uptake in whole-body radioactive iodine scans (WBS) in papillary...

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Autores principales: Suh, Sunghwan, Kim, Yun Hak, Goh, Tae Sik, Jeong, Dae Cheon, Lee, Chi-Seung, Jang, Jeon Yeob, Cha, Wonjae, Han, Myoung-Eun, Kim, Seong-Jang, Kim, In Joo, Pak, Kyoungjune
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Yonsei University College of Medicine 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6037592/
https://www.ncbi.nlm.nih.gov/pubmed/29978611
http://dx.doi.org/10.3349/ymj.2018.59.6.746
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author Suh, Sunghwan
Kim, Yun Hak
Goh, Tae Sik
Jeong, Dae Cheon
Lee, Chi-Seung
Jang, Jeon Yeob
Cha, Wonjae
Han, Myoung-Eun
Kim, Seong-Jang
Kim, In Joo
Pak, Kyoungjune
author_facet Suh, Sunghwan
Kim, Yun Hak
Goh, Tae Sik
Jeong, Dae Cheon
Lee, Chi-Seung
Jang, Jeon Yeob
Cha, Wonjae
Han, Myoung-Eun
Kim, Seong-Jang
Kim, In Joo
Pak, Kyoungjune
author_sort Suh, Sunghwan
collection PubMed
description PURPOSE: The present study investigated the dynamics and prognostic role of messenger RNA (mRNA) expression responsible for (18)F-fluorodeoxyglucose (FDG) uptake in FDG positron emission tomography (PET) and radioactive iodine ((131)I) uptake in whole-body radioactive iodine scans (WBS) in papillary thyroid cancer (PTC) patients. MATERIALS AND METHODS: The primary and processed data were downloaded from the Genomic Data Commons Data Portal. Expression data for sodium/iodide symporter (solute carrier family 5 member 5, SLC5A5), hexokinase (HK1–3), glucose-6-phosphate dehydrogenase (G6PD), and glucose transporter (solute carrier family 2, SLC2A1–4) mRNA were collected. RESULTS: Expression of SLC5A5 mRNA were negatively correlated with SLC2A1 mRNA and positively correlated with SLC2A4 mRNA. In PTC with BRAF mutations, expressions of SLC2A1, SLC2A3, HK2, and HK3 mRNA were higher than those in PTC without BRAF mutations. Expression of SLC5A5, SLC2A4, HK1, and G6PD mRNA was lower in PTC without BRAF mutation. PTCs with higher expression of SLC5A5 mRNA had more favorable disease-free survival, but no association with overall survival. CONCLUSION: Expression of SLC5A5 mRNA was negatively correlated with SLC2A1 mRNA. This finding provides a molecular basis for the management of PTC with negative WBS using (18)F-FDG PET scans. In addition, higher expression of SLC5A5 mRNA was associated with less PTC recurrence, but not with deaths.
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spelling pubmed-60375922018-08-01 mRNA Expression of SLC5A5 and SLC2A Family Genes in Papillary Thyroid Cancer: An Analysis of The Cancer Genome Atlas Suh, Sunghwan Kim, Yun Hak Goh, Tae Sik Jeong, Dae Cheon Lee, Chi-Seung Jang, Jeon Yeob Cha, Wonjae Han, Myoung-Eun Kim, Seong-Jang Kim, In Joo Pak, Kyoungjune Yonsei Med J Original Article PURPOSE: The present study investigated the dynamics and prognostic role of messenger RNA (mRNA) expression responsible for (18)F-fluorodeoxyglucose (FDG) uptake in FDG positron emission tomography (PET) and radioactive iodine ((131)I) uptake in whole-body radioactive iodine scans (WBS) in papillary thyroid cancer (PTC) patients. MATERIALS AND METHODS: The primary and processed data were downloaded from the Genomic Data Commons Data Portal. Expression data for sodium/iodide symporter (solute carrier family 5 member 5, SLC5A5), hexokinase (HK1–3), glucose-6-phosphate dehydrogenase (G6PD), and glucose transporter (solute carrier family 2, SLC2A1–4) mRNA were collected. RESULTS: Expression of SLC5A5 mRNA were negatively correlated with SLC2A1 mRNA and positively correlated with SLC2A4 mRNA. In PTC with BRAF mutations, expressions of SLC2A1, SLC2A3, HK2, and HK3 mRNA were higher than those in PTC without BRAF mutations. Expression of SLC5A5, SLC2A4, HK1, and G6PD mRNA was lower in PTC without BRAF mutation. PTCs with higher expression of SLC5A5 mRNA had more favorable disease-free survival, but no association with overall survival. CONCLUSION: Expression of SLC5A5 mRNA was negatively correlated with SLC2A1 mRNA. This finding provides a molecular basis for the management of PTC with negative WBS using (18)F-FDG PET scans. In addition, higher expression of SLC5A5 mRNA was associated with less PTC recurrence, but not with deaths. Yonsei University College of Medicine 2018-08-01 2018-07-04 /pmc/articles/PMC6037592/ /pubmed/29978611 http://dx.doi.org/10.3349/ymj.2018.59.6.746 Text en © Copyright: Yonsei University College of Medicine 2018 http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Suh, Sunghwan
Kim, Yun Hak
Goh, Tae Sik
Jeong, Dae Cheon
Lee, Chi-Seung
Jang, Jeon Yeob
Cha, Wonjae
Han, Myoung-Eun
Kim, Seong-Jang
Kim, In Joo
Pak, Kyoungjune
mRNA Expression of SLC5A5 and SLC2A Family Genes in Papillary Thyroid Cancer: An Analysis of The Cancer Genome Atlas
title mRNA Expression of SLC5A5 and SLC2A Family Genes in Papillary Thyroid Cancer: An Analysis of The Cancer Genome Atlas
title_full mRNA Expression of SLC5A5 and SLC2A Family Genes in Papillary Thyroid Cancer: An Analysis of The Cancer Genome Atlas
title_fullStr mRNA Expression of SLC5A5 and SLC2A Family Genes in Papillary Thyroid Cancer: An Analysis of The Cancer Genome Atlas
title_full_unstemmed mRNA Expression of SLC5A5 and SLC2A Family Genes in Papillary Thyroid Cancer: An Analysis of The Cancer Genome Atlas
title_short mRNA Expression of SLC5A5 and SLC2A Family Genes in Papillary Thyroid Cancer: An Analysis of The Cancer Genome Atlas
title_sort mrna expression of slc5a5 and slc2a family genes in papillary thyroid cancer: an analysis of the cancer genome atlas
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6037592/
https://www.ncbi.nlm.nih.gov/pubmed/29978611
http://dx.doi.org/10.3349/ymj.2018.59.6.746
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