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Systematic analysis on expression quantitative trait loci identifies a novel regulatory variant in ring finger and WD repeat domain 3 associated with prognosis of pancreatic cancer

BACKGROUND: Pancreatic adenocarcinoma (PAAD) is an extremely lethal malignancy. Identification of the functional genes and genetic variants related to PAAD prognosis is important and challenging. Previously identified prognostic genes from several expression profile analyses were inconsistent. The r...

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Autores principales: Zhu, Ying, Peng, Xiating, Wang, Xiaoyang, Ying, Pingting, Wang, Haoxue, Li, Bin, Li, Yue, Zhang, Ming, Cai, Yimin, Lu, Zequn, Niu, Siyuan, Yang, Nan, Zhong, Rong, Tian, Jianbo, Chang, Jiang, Miao, Xiaoping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433068/
https://www.ncbi.nlm.nih.gov/pubmed/35830250
http://dx.doi.org/10.1097/CM9.0000000000002180
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author Zhu, Ying
Peng, Xiating
Wang, Xiaoyang
Ying, Pingting
Wang, Haoxue
Li, Bin
Li, Yue
Zhang, Ming
Cai, Yimin
Lu, Zequn
Niu, Siyuan
Yang, Nan
Zhong, Rong
Tian, Jianbo
Chang, Jiang
Miao, Xiaoping
author_facet Zhu, Ying
Peng, Xiating
Wang, Xiaoyang
Ying, Pingting
Wang, Haoxue
Li, Bin
Li, Yue
Zhang, Ming
Cai, Yimin
Lu, Zequn
Niu, Siyuan
Yang, Nan
Zhong, Rong
Tian, Jianbo
Chang, Jiang
Miao, Xiaoping
author_sort Zhu, Ying
collection PubMed
description BACKGROUND: Pancreatic adenocarcinoma (PAAD) is an extremely lethal malignancy. Identification of the functional genes and genetic variants related to PAAD prognosis is important and challenging. Previously identified prognostic genes from several expression profile analyses were inconsistent. The regulatory genetic variants that affect PAAD prognosis were largely unknown. METHODS: Firstly, a meta-analysis was performed with seven published datasets to systematically explore the candidate prognostic genes for PAAD. Next, to identify the regulatory variants for those candidate genes, expression quantitative trait loci analysis was implemented with PAAD data resources from The Cancer Genome Atlas. Then, a two-stage association study in a total of 893 PAAD patients was conducted to interrogate the regulatory variants and find the prognostic locus. Finally, a series of biochemical experiments and phenotype assays were carried out to demonstrate the biological function of variation and genes in PAAD progression process. RESULTS: A total of 128 genes were identified associated with the PAAD prognosis in the meta-analysis. Fourteen regulatory loci in 12 of the 128 genes were discovered, among which, only rs4887783, the functional variant in the promoter of Ring Finger and WD Repeat Domain 3 (RFWD3), presented significant association with PAAD prognosis in both stages of the population study. Dual-luciferase reporter and electrophoretic mobility shift assays demonstrated that rs4887783-G allele, which predicts the worse prognosis, enhanced the binding of transcript factor REST, thus elevating RFWD3 expression. Further phenotypic assays revealed that excess expression of RFWD3 promoted tumor cell migration without affecting their proliferation rate. RFWD3 was highly expressed in PAAD and might orchestrate the genes in the DNA repair process. CONCLUSIONS: RFWD3 and its regulatory variant are novel genetic factors for PAAD prognosis.
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spelling pubmed-94330682022-09-01 Systematic analysis on expression quantitative trait loci identifies a novel regulatory variant in ring finger and WD repeat domain 3 associated with prognosis of pancreatic cancer Zhu, Ying Peng, Xiating Wang, Xiaoyang Ying, Pingting Wang, Haoxue Li, Bin Li, Yue Zhang, Ming Cai, Yimin Lu, Zequn Niu, Siyuan Yang, Nan Zhong, Rong Tian, Jianbo Chang, Jiang Miao, Xiaoping Chin Med J (Engl) Original Articles BACKGROUND: Pancreatic adenocarcinoma (PAAD) is an extremely lethal malignancy. Identification of the functional genes and genetic variants related to PAAD prognosis is important and challenging. Previously identified prognostic genes from several expression profile analyses were inconsistent. The regulatory genetic variants that affect PAAD prognosis were largely unknown. METHODS: Firstly, a meta-analysis was performed with seven published datasets to systematically explore the candidate prognostic genes for PAAD. Next, to identify the regulatory variants for those candidate genes, expression quantitative trait loci analysis was implemented with PAAD data resources from The Cancer Genome Atlas. Then, a two-stage association study in a total of 893 PAAD patients was conducted to interrogate the regulatory variants and find the prognostic locus. Finally, a series of biochemical experiments and phenotype assays were carried out to demonstrate the biological function of variation and genes in PAAD progression process. RESULTS: A total of 128 genes were identified associated with the PAAD prognosis in the meta-analysis. Fourteen regulatory loci in 12 of the 128 genes were discovered, among which, only rs4887783, the functional variant in the promoter of Ring Finger and WD Repeat Domain 3 (RFWD3), presented significant association with PAAD prognosis in both stages of the population study. Dual-luciferase reporter and electrophoretic mobility shift assays demonstrated that rs4887783-G allele, which predicts the worse prognosis, enhanced the binding of transcript factor REST, thus elevating RFWD3 expression. Further phenotypic assays revealed that excess expression of RFWD3 promoted tumor cell migration without affecting their proliferation rate. RFWD3 was highly expressed in PAAD and might orchestrate the genes in the DNA repair process. CONCLUSIONS: RFWD3 and its regulatory variant are novel genetic factors for PAAD prognosis. Lippincott Williams & Wilkins 2022-06-05 2022-07-13 /pmc/articles/PMC9433068/ /pubmed/35830250 http://dx.doi.org/10.1097/CM9.0000000000002180 Text en Copyright © 2022 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Original Articles
Zhu, Ying
Peng, Xiating
Wang, Xiaoyang
Ying, Pingting
Wang, Haoxue
Li, Bin
Li, Yue
Zhang, Ming
Cai, Yimin
Lu, Zequn
Niu, Siyuan
Yang, Nan
Zhong, Rong
Tian, Jianbo
Chang, Jiang
Miao, Xiaoping
Systematic analysis on expression quantitative trait loci identifies a novel regulatory variant in ring finger and WD repeat domain 3 associated with prognosis of pancreatic cancer
title Systematic analysis on expression quantitative trait loci identifies a novel regulatory variant in ring finger and WD repeat domain 3 associated with prognosis of pancreatic cancer
title_full Systematic analysis on expression quantitative trait loci identifies a novel regulatory variant in ring finger and WD repeat domain 3 associated with prognosis of pancreatic cancer
title_fullStr Systematic analysis on expression quantitative trait loci identifies a novel regulatory variant in ring finger and WD repeat domain 3 associated with prognosis of pancreatic cancer
title_full_unstemmed Systematic analysis on expression quantitative trait loci identifies a novel regulatory variant in ring finger and WD repeat domain 3 associated with prognosis of pancreatic cancer
title_short Systematic analysis on expression quantitative trait loci identifies a novel regulatory variant in ring finger and WD repeat domain 3 associated with prognosis of pancreatic cancer
title_sort systematic analysis on expression quantitative trait loci identifies a novel regulatory variant in ring finger and wd repeat domain 3 associated with prognosis of pancreatic cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433068/
https://www.ncbi.nlm.nih.gov/pubmed/35830250
http://dx.doi.org/10.1097/CM9.0000000000002180
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