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A genetic variant in miR‐100 is a protective factor of childhood acute lymphoblastic leukemia
BACKGROUND: In the past decade, miR‐100, miR‐146a, and miR‐210 were reported to be dysregulated in childhood acute lymphoblastic leukemia (ALL). However, effects of genetic variants in these three microRNAs have not been investigated in Chinese population. METHODS: In this study, we conducted a case...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536980/ https://www.ncbi.nlm.nih.gov/pubmed/30848099 http://dx.doi.org/10.1002/cam4.2082 |
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author | Xue, Yao Yang, Xiaoyun Hu, Shaoyan Kang, Meiyun Chen, Jing Fang, Yongjun |
author_facet | Xue, Yao Yang, Xiaoyun Hu, Shaoyan Kang, Meiyun Chen, Jing Fang, Yongjun |
author_sort | Xue, Yao |
collection | PubMed |
description | BACKGROUND: In the past decade, miR‐100, miR‐146a, and miR‐210 were reported to be dysregulated in childhood acute lymphoblastic leukemia (ALL). However, effects of genetic variants in these three microRNAs have not been investigated in Chinese population. METHODS: In this study, we conducted a case‐control study to evaluate the relationship between genetic variants in miR‐100, miR‐146a, and miR‐210 and the risk of childhood ALL in Chinese population. Subsequently, plasma expression level of miR‐100 was also detected. RESULT: We found that subjects carrying mutant homozygous TT genotype of miR‐100 rs543412 had a statistically significantly decreased risk of childhood ALL (adjusted odds ratio [OR] = 0.73, 95% confidence interval [CI] = 0.55‐0.97, P = 0.029). This protective effect was also observed among subjects whose parents were ever drinkers (adjusted OR = 0.53, 95% CI = 0.29‐0.94), or whose living house were ever painted (adjusted OR = 0.57, 95% CI = 0.34‐0.94). Besides, rs543412 variant homozygous TT had a significantly protective role in patients with childhood B‐ALL. Finally, we found that expression level of miR‐100 in plasma of childhood ALL cases was significantly higher than that of noncancer controls. CONCLUSION: Our study suggested that there was significant association between the polymorphisms in miR‐100 (rs543412) and decreased susceptibility to childhood ALL. |
format | Online Article Text |
id | pubmed-6536980 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65369802019-06-03 A genetic variant in miR‐100 is a protective factor of childhood acute lymphoblastic leukemia Xue, Yao Yang, Xiaoyun Hu, Shaoyan Kang, Meiyun Chen, Jing Fang, Yongjun Cancer Med Cancer Prevention BACKGROUND: In the past decade, miR‐100, miR‐146a, and miR‐210 were reported to be dysregulated in childhood acute lymphoblastic leukemia (ALL). However, effects of genetic variants in these three microRNAs have not been investigated in Chinese population. METHODS: In this study, we conducted a case‐control study to evaluate the relationship between genetic variants in miR‐100, miR‐146a, and miR‐210 and the risk of childhood ALL in Chinese population. Subsequently, plasma expression level of miR‐100 was also detected. RESULT: We found that subjects carrying mutant homozygous TT genotype of miR‐100 rs543412 had a statistically significantly decreased risk of childhood ALL (adjusted odds ratio [OR] = 0.73, 95% confidence interval [CI] = 0.55‐0.97, P = 0.029). This protective effect was also observed among subjects whose parents were ever drinkers (adjusted OR = 0.53, 95% CI = 0.29‐0.94), or whose living house were ever painted (adjusted OR = 0.57, 95% CI = 0.34‐0.94). Besides, rs543412 variant homozygous TT had a significantly protective role in patients with childhood B‐ALL. Finally, we found that expression level of miR‐100 in plasma of childhood ALL cases was significantly higher than that of noncancer controls. CONCLUSION: Our study suggested that there was significant association between the polymorphisms in miR‐100 (rs543412) and decreased susceptibility to childhood ALL. John Wiley and Sons Inc. 2019-03-07 /pmc/articles/PMC6536980/ /pubmed/30848099 http://dx.doi.org/10.1002/cam4.2082 Text en © 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Cancer Prevention Xue, Yao Yang, Xiaoyun Hu, Shaoyan Kang, Meiyun Chen, Jing Fang, Yongjun A genetic variant in miR‐100 is a protective factor of childhood acute lymphoblastic leukemia |
title | A genetic variant in miR‐100 is a protective factor of childhood acute lymphoblastic leukemia |
title_full | A genetic variant in miR‐100 is a protective factor of childhood acute lymphoblastic leukemia |
title_fullStr | A genetic variant in miR‐100 is a protective factor of childhood acute lymphoblastic leukemia |
title_full_unstemmed | A genetic variant in miR‐100 is a protective factor of childhood acute lymphoblastic leukemia |
title_short | A genetic variant in miR‐100 is a protective factor of childhood acute lymphoblastic leukemia |
title_sort | genetic variant in mir‐100 is a protective factor of childhood acute lymphoblastic leukemia |
topic | Cancer Prevention |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536980/ https://www.ncbi.nlm.nih.gov/pubmed/30848099 http://dx.doi.org/10.1002/cam4.2082 |
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