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Impact of LINC00673 genetic variants on uterine cervical cancer clinicopathologic characteristics

To date, no study delineates the relationships among the genetic variants of long intergenic noncoding RNA 673 (LINC00673) and uterine cervical carcinogenesis as well as clinicopathological parameters and 5 years survival of cervical cancer patients in Taiwan. Therefore, the involvement of LINC00673...

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Autores principales: Sun, Yi-Hung, Chen, Liang-Jou, Wang, Chun-Hao, Lee, Chung-Yuan, Hsiao, Yi-Hsuan, Yang, Shun-Fa, Wang, Po-Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10475370/
https://www.ncbi.nlm.nih.gov/pubmed/37670967
http://dx.doi.org/10.7150/jca.86678
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author Sun, Yi-Hung
Chen, Liang-Jou
Wang, Chun-Hao
Lee, Chung-Yuan
Hsiao, Yi-Hsuan
Yang, Shun-Fa
Wang, Po-Hui
author_facet Sun, Yi-Hung
Chen, Liang-Jou
Wang, Chun-Hao
Lee, Chung-Yuan
Hsiao, Yi-Hsuan
Yang, Shun-Fa
Wang, Po-Hui
author_sort Sun, Yi-Hung
collection PubMed
description To date, no study delineates the relationships among the genetic variants of long intergenic noncoding RNA 673 (LINC00673) and uterine cervical carcinogenesis as well as clinicopathological parameters and 5 years survival of cervical cancer patients in Taiwan. Therefore, the involvement of LINC00673 polymorphisms in cervical cancer was investigated. Genotypic frequencies of three LINC00673 polymorphisms rs6501551, rs9914618 and rs11655237 were determined in 199 patients including 115 patients with invasive cancer, 84 with precancerous lesions, and 274 control females using real-time polymerase chain reaction. It revealed that LINC00673 polymorphisms were not found significantly related to development of cervical cancer. Cervical cancer patients with genotypes AG/GG in LINC00673 rs6501551 had more risk to have tumor diameter larger than 4 cm as compared to those with genotype AA (p=0.043). Cervical cancer patients with genotype GG in rs6501551 had worse 5 years survival as compared to those with genotypes AA/AG in multivariate analysis (hazard ratio: 4.70; p=0.097). However, only two patients exhibiting GG were noted, and one had mortality, another had no mortality. In conclusion, larger sample size needs to verify the associations of LINC00673 genetic variants with clinicopathological parameters and patient survival of cervical cancer for Taiwanese females.
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spelling pubmed-104753702023-09-05 Impact of LINC00673 genetic variants on uterine cervical cancer clinicopathologic characteristics Sun, Yi-Hung Chen, Liang-Jou Wang, Chun-Hao Lee, Chung-Yuan Hsiao, Yi-Hsuan Yang, Shun-Fa Wang, Po-Hui J Cancer Research Paper To date, no study delineates the relationships among the genetic variants of long intergenic noncoding RNA 673 (LINC00673) and uterine cervical carcinogenesis as well as clinicopathological parameters and 5 years survival of cervical cancer patients in Taiwan. Therefore, the involvement of LINC00673 polymorphisms in cervical cancer was investigated. Genotypic frequencies of three LINC00673 polymorphisms rs6501551, rs9914618 and rs11655237 were determined in 199 patients including 115 patients with invasive cancer, 84 with precancerous lesions, and 274 control females using real-time polymerase chain reaction. It revealed that LINC00673 polymorphisms were not found significantly related to development of cervical cancer. Cervical cancer patients with genotypes AG/GG in LINC00673 rs6501551 had more risk to have tumor diameter larger than 4 cm as compared to those with genotype AA (p=0.043). Cervical cancer patients with genotype GG in rs6501551 had worse 5 years survival as compared to those with genotypes AA/AG in multivariate analysis (hazard ratio: 4.70; p=0.097). However, only two patients exhibiting GG were noted, and one had mortality, another had no mortality. In conclusion, larger sample size needs to verify the associations of LINC00673 genetic variants with clinicopathological parameters and patient survival of cervical cancer for Taiwanese females. Ivyspring International Publisher 2023-08-15 /pmc/articles/PMC10475370/ /pubmed/37670967 http://dx.doi.org/10.7150/jca.86678 Text en © The author(s) 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/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Sun, Yi-Hung
Chen, Liang-Jou
Wang, Chun-Hao
Lee, Chung-Yuan
Hsiao, Yi-Hsuan
Yang, Shun-Fa
Wang, Po-Hui
Impact of LINC00673 genetic variants on uterine cervical cancer clinicopathologic characteristics
title Impact of LINC00673 genetic variants on uterine cervical cancer clinicopathologic characteristics
title_full Impact of LINC00673 genetic variants on uterine cervical cancer clinicopathologic characteristics
title_fullStr Impact of LINC00673 genetic variants on uterine cervical cancer clinicopathologic characteristics
title_full_unstemmed Impact of LINC00673 genetic variants on uterine cervical cancer clinicopathologic characteristics
title_short Impact of LINC00673 genetic variants on uterine cervical cancer clinicopathologic characteristics
title_sort impact of linc00673 genetic variants on uterine cervical cancer clinicopathologic characteristics
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10475370/
https://www.ncbi.nlm.nih.gov/pubmed/37670967
http://dx.doi.org/10.7150/jca.86678
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