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The ryanodine receptor mutational characteristics and its indication for cancer prognosis
Ca(2+) signaling is altered substantially in many cancers. The ryanodine receptors (RYRs) are among the key ion channels in Ca(2+) signaling. This study aimed to establish the mutational profile of RYR in cancers and investigate the correlation between RYR alterations and cancer phenotypes. The soma...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9515073/ https://www.ncbi.nlm.nih.gov/pubmed/36167878 http://dx.doi.org/10.1038/s41598-022-19905-y |
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author | Wang, Fenglin Yu, Jingbo Lin, Ping Sigalas, Charalampos Zhang, Shibo Gong, Yuan Sitsapesan, Rebecca Song, Lele |
author_facet | Wang, Fenglin Yu, Jingbo Lin, Ping Sigalas, Charalampos Zhang, Shibo Gong, Yuan Sitsapesan, Rebecca Song, Lele |
author_sort | Wang, Fenglin |
collection | PubMed |
description | Ca(2+) signaling is altered substantially in many cancers. The ryanodine receptors (RYRs) are among the key ion channels in Ca(2+) signaling. This study aimed to establish the mutational profile of RYR in cancers and investigate the correlation between RYR alterations and cancer phenotypes. The somatic mutation and clinical data of 11,000 cancer patients across 33 cancer types was downloaded from The Cancer Genome Atlas (TCGA) database. Subsequent data processing was performed with corresponding packages of the R software. Mutational profile was analyzed and its correlation with tumor mutational burden (TMB), patient prognosis, age and smoking status was analyzed and compared. All three RYR isoforms exhibited random mutational distribution without hotspot mutations when all cancers were analyzed together. The number of mutations in RYR2 (2388 mutations) far overweight that of RYR1 (1439 mutations) and RYR3 (1573 mutations). Linear correlation was observed between cumulative TMB and cumulative number of mutations for all RYR isoforms. Patients with RYR mutations exhibited significantly higher TMB than those without RYR mutations for most cancer types. Strong correlation was also revealed in the average number of mutations per person between pairs of RYR isoforms. No stratification of patient overall survival (OS) by mutational status was found for all three RYR isoforms when all cancers were analyzed together, however, significant stratification of OS by RYR mutations was revealed in several individual cancers, most strikingly in LUAD (P = 0.0067, RYR1), BLCA (P = 0.00071, RYR2), LUSC (P = 0.036, RYR2) and KIRC (P = 0.0042, RYR3). Furthermore, RYR mutations were correlated with higher age, higher smoking history grading and higher number of pack years. Characteristic mutation profile of RYRs in cancers has been revealed for the first time. RYR mutations were correlated with TMB, age, smoking status and capable of stratifying the prognosis of patients in several cancer types. |
format | Online Article Text |
id | pubmed-9515073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95150732022-09-29 The ryanodine receptor mutational characteristics and its indication for cancer prognosis Wang, Fenglin Yu, Jingbo Lin, Ping Sigalas, Charalampos Zhang, Shibo Gong, Yuan Sitsapesan, Rebecca Song, Lele Sci Rep Article Ca(2+) signaling is altered substantially in many cancers. The ryanodine receptors (RYRs) are among the key ion channels in Ca(2+) signaling. This study aimed to establish the mutational profile of RYR in cancers and investigate the correlation between RYR alterations and cancer phenotypes. The somatic mutation and clinical data of 11,000 cancer patients across 33 cancer types was downloaded from The Cancer Genome Atlas (TCGA) database. Subsequent data processing was performed with corresponding packages of the R software. Mutational profile was analyzed and its correlation with tumor mutational burden (TMB), patient prognosis, age and smoking status was analyzed and compared. All three RYR isoforms exhibited random mutational distribution without hotspot mutations when all cancers were analyzed together. The number of mutations in RYR2 (2388 mutations) far overweight that of RYR1 (1439 mutations) and RYR3 (1573 mutations). Linear correlation was observed between cumulative TMB and cumulative number of mutations for all RYR isoforms. Patients with RYR mutations exhibited significantly higher TMB than those without RYR mutations for most cancer types. Strong correlation was also revealed in the average number of mutations per person between pairs of RYR isoforms. No stratification of patient overall survival (OS) by mutational status was found for all three RYR isoforms when all cancers were analyzed together, however, significant stratification of OS by RYR mutations was revealed in several individual cancers, most strikingly in LUAD (P = 0.0067, RYR1), BLCA (P = 0.00071, RYR2), LUSC (P = 0.036, RYR2) and KIRC (P = 0.0042, RYR3). Furthermore, RYR mutations were correlated with higher age, higher smoking history grading and higher number of pack years. Characteristic mutation profile of RYRs in cancers has been revealed for the first time. RYR mutations were correlated with TMB, age, smoking status and capable of stratifying the prognosis of patients in several cancer types. Nature Publishing Group UK 2022-09-27 /pmc/articles/PMC9515073/ /pubmed/36167878 http://dx.doi.org/10.1038/s41598-022-19905-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wang, Fenglin Yu, Jingbo Lin, Ping Sigalas, Charalampos Zhang, Shibo Gong, Yuan Sitsapesan, Rebecca Song, Lele The ryanodine receptor mutational characteristics and its indication for cancer prognosis |
title | The ryanodine receptor mutational characteristics and its indication for cancer prognosis |
title_full | The ryanodine receptor mutational characteristics and its indication for cancer prognosis |
title_fullStr | The ryanodine receptor mutational characteristics and its indication for cancer prognosis |
title_full_unstemmed | The ryanodine receptor mutational characteristics and its indication for cancer prognosis |
title_short | The ryanodine receptor mutational characteristics and its indication for cancer prognosis |
title_sort | ryanodine receptor mutational characteristics and its indication for cancer prognosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9515073/ https://www.ncbi.nlm.nih.gov/pubmed/36167878 http://dx.doi.org/10.1038/s41598-022-19905-y |
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