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

Author:

Vymetalkova Veronika123ORCID,Rosa Fabio4,Susova Simona35,Bendova Petra13,Levy Miroslav6,Buchler Tomas7,Kral Jan8,Bartu Linda1,Vodickova Ludmila123,Hughes David J9,Soucek Pavel35,Naccarati Alessio14,Kumar Rajiv1011,Vodicka Pavel123,Pardini Barbara412

Affiliation:

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

2. Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University, Prague, Czech Republic

3. Biomedical Centre, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic

4. IIGM Italian Institute for Genomic Medicine, Turin, Italy

5. Toxicogenomics Unit, National Institute of Public Health, Prague, Czech Republic

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

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

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

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

10. Division of Molecular Genetic Epidemiology

11. Division of Functional Genome Analysis, German Cancer Research Centre, Heidelberg, Germany

12. Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Italy

Abstract

Abstract 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.

Funder

Grant Agency of the Ministry of Health of the Czech Republic

Grant Agency of the Czech Republic

Grant Agency of Charles University

European Cooperation in Science and Technology

Publisher

Oxford University Press (OUP)

Subject

Health, Toxicology and Mutagenesis,Genetics (clinical),Toxicology,Genetics

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