Expression quantitative trait loci in ABC transporters are associated with survival in 5-FU treated colorectal cancer patients.


Journal

Mutagenesis
ISSN: 1464-3804
Titre abrégé: Mutagenesis
Pays: England
ID NLM: 8707812

Informations de publication

Date de publication:
11 07 2020
Historique:
received: 20 09 2019
accepted: 05 12 2019
pubmed: 11 1 2020
medline: 9 2 2021
entrez: 11 1 2020
Statut: ppublish

Résumé

The chemotherapeutic efficacy in colorectal cancer (CRC) is limited due to the inter-individual variability in drug response and the development of tumour resistance. ATP-binding cassette (ABC) transporters are crucial in the development of resistance by the efflux of anticancer agents from cancer cells. In this study, we identified 14 single nucleotide polymorphisms (SNPs) in 11 ABC transporter genes acting as an expression of quantitative trait loci (eQTLs), i.e. whose variation influence the expression of many downstream genes. These SNPs were genotyped in a case-control study comprising 1098 cases and 1442 healthy controls and analysed in relation to CRC development risk and patient survival. Considering a strict correction for multiple tests, we did not observe any significant association between SNPs and CRC risk. The rs3819720 polymorphism in the ABCB3/TAP2 gene was statistically significantly associated with shorter overall survival (OS) in the codominant, and dominant models [GA vs. GG, hazard ratio (HR) = 1.48; P = 0.002; AA vs. GG, HR = 1.70; P = 0.004 and GA + AA vs. GG, HR = 1.52; P = 0.0006]. Additionally, GA carriers of the same SNP displayed worse OS after receiving 5-FU based chemotherapy. The variant allele of rs3819720 polymorphism statistically significantly affected the expression of 36 downstream genes. Screening for eQTL polymorphisms in relevant genes such as ABC transporters that can regulate the expression of several other genes may help to identify the genetic background involved in the individual response to the treatment of CRC patients.

Identifiants

pubmed: 31922572
pii: 5699895
doi: 10.1093/mutage/gez050
doi:

Substances chimiques

ATP-Binding Cassette Transporters 0
Fluorouracil U3P01618RT

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

273-281

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of the UK Environmental Mutagen Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Veronika Vymetalkova (V)

Department of Molecular Biology of Cancer, Institute of Experimental Medicine, Prague, Czech Republic.
Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Biomedical Centre, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.

Fabio Rosa (F)

IIGM Italian Institute for Genomic Medicine, Turin, Italy.

Simona Susova (S)

Biomedical Centre, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Toxicogenomics Unit, National Institute of Public Health, Prague, Czech Republic.

Petra Bendova (P)

Department of Molecular Biology of Cancer, Institute of Experimental Medicine, Prague, Czech Republic.
Biomedical Centre, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.

Miroslav Levy (M)

Department of Surgery, First Faculty of Medicine, Charles University and Thomayer Hospital, Prague, Czech Republic.

Tomas Buchler (T)

Department of Oncology, First Faculty of Medicine, Charles University and Thomayer Hospital, Prague, Czech Republic.

Jan Kral (J)

Institute for Clinical and Experimental Medicine, IKEM, Prague, Czech Republic.

Linda Bartu (L)

Department of Molecular Biology of Cancer, Institute of Experimental Medicine, Prague, Czech Republic.

Ludmila Vodickova (L)

Department of Molecular Biology of Cancer, Institute of Experimental Medicine, Prague, Czech Republic.
Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Biomedical Centre, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.

David J Hughes (DJ)

Cancer Biology and Therapeutics Group, UCD Conway Institute, School of Biomolecular and Biomedical Science, University College Dublin, Dublin, Ireland.

Pavel Soucek (P)

Biomedical Centre, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Toxicogenomics Unit, National Institute of Public Health, Prague, Czech Republic.

Alessio Naccarati (A)

Department of Molecular Biology of Cancer, Institute of Experimental Medicine, Prague, Czech Republic.
IIGM Italian Institute for Genomic Medicine, Turin, Italy.

Rajiv Kumar (R)

Division of Molecular Genetic Epidemiology.
Division of Functional Genome Analysis, German Cancer Research Centre, Heidelberg, Germany.

Pavel Vodicka (P)

Department of Molecular Biology of Cancer, Institute of Experimental Medicine, Prague, Czech Republic.
Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Biomedical Centre, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.

Barbara Pardini (B)

IIGM Italian Institute for Genomic Medicine, Turin, Italy.
Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Italy.

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Classifications MeSH