Skip to main content
Top
Published in: BMC Cancer 1/2021

Open Access 01-12-2021 | Lung Cancer | Research

Genetic polymorphisms and haplotypes of ERCC1 and ERCC2 associated with quality of life, depression, and anxiety status among patients with lung cancer

Authors: Yunxiang Tang, Ruike Zhang, Yinan Li, Shuyu Xu, Hao Wang, Jingzhou Xu, Lei Xiao, Yajing Wang, Jing Du, Yujia Huang, Tong Su

Published in: BMC Cancer | Issue 1/2021

Login to get access

Abstract

Background

Patients with lung cancer (LC) have a poor quality of life (QoL) and easily suffer from psychological diseases. Previous studies focused less on the relationship between genetic factors and QoL, depression, and anxiety status in LC patients. The current study is intended to explore the relationship between SNPs and haplotypes of ERCC1 and ERCC2 and the QoL, depression and anxiety status of patients with LC.

Methods

QoL, depression and anxiety status were assessed in 291 LC patients using the European Organization for Research and Treatment of Cancer (EORTC) Core Quality of Life Questionnaire (QLQ-C30), EORTC Quality of Life Questionnaire-Lung Cancer 13 (QLQ-LC13), SDS and SAS. Nine tag SNPs of ERCC1 and ERCC2 were detected using an improved multiplex ligation detection reaction (iMLDR) technique. Haplotype analysis was conducted using the software Haploview 4.2. The association between SNPs or haplotypes and QoL or depression or anxiety in LC patients was analyzed by regression analysis.

Results

ERCC1 rs11615 was associated with emotional functioning (P = 0.027), and ERCC1 rs3212986 was associated with anxiety scores (P = 0.018). ERCC1 rs762562-rs3212986 haplotype was associated with cognitive function (P = 0.029), somatic function (P = 0.014) and dysphagia (OR = 3.32, P = 0.044). Patients with ERCC1 rs3212986-rs11615 AG haplotype had worse cognitive function (adjusted Beta = − 5.42) and somatic function (adjusted Beta = − 6.55) and had severer symptoms of loss of appetite (adjusted OR = 1.67) and dysphagia (adjusted OR = 4.43) (All adjusted P < 0.05). ERCC2 rs13181-rs3916874-rs238416 haplotype was associated with emotional functioning (P = 0.035), pain at other sites (OR 1.88, P = 0.014), chest pain (OR 0.42, P = 0.02), dysphagia (OR 2.82, P = 0.048), and anxiety status (OR 0.23, P = 0.009).

Conclusion

After adjustment for environmental factors, SNPs and haplotypes of ERCC1 and ERCC2 were associated with different domains of QoL, depression and anxiety in LC patients.
Appendix
Available only for authorised users
Literature
11.
go back to reference Tan LM, Qiu CF, Zhu T, Jin YX, Li X, Yin JY, et al. Genetic polymorphisms and platinum-based chemotherapy treatment outcomes in patients with non-small cell lung Cancer: a genetic epidemiology study based meta-analysis. Sci Rep-Uk. 2017;7(1):5593. https://doi.org/10.1038/s41598-017-05642-0. Tan LM, Qiu CF, Zhu T, Jin YX, Li X, Yin JY, et al. Genetic polymorphisms and platinum-based chemotherapy treatment outcomes in patients with non-small cell lung Cancer: a genetic epidemiology study based meta-analysis. Sci Rep-Uk. 2017;7(1):5593. https://​doi.​org/​10.​1038/​s41598-017-05642-0.
16.
go back to reference Thomas G, Sinville R, Sutton S, Farquar H, Hammer RP, Soper SA, et al. Capillary and microelectrophoretic separations of ligase detection reaction products produced from low-abundant point mutations in genomic DNA. Electrophoresis. 2010;25(10–11):1668–77. Thomas G, Sinville R, Sutton S, Farquar H, Hammer RP, Soper SA, et al. Capillary and microelectrophoretic separations of ligase detection reaction products produced from low-abundant point mutations in genomic DNA. Electrophoresis. 2010;25(10–11):1668–77.
21.
go back to reference Peter F, Simon W, Desmond C. EORTC QLQ-C30 Reference Values; 2008. Peter F, Simon W, Desmond C. EORTC QLQ-C30 Reference Values; 2008.
26.
go back to reference Grenda A, Bach J, Krawczyk P, Nico M, Milanowski J. P2.01–44 promoter polymorphisms of TOP2A and ERCC1 genes as predictive factors for chemotherapy in non-small cell lung cancer patients. J Thorac Oncol. 2019;14(10):S656.CrossRef Grenda A, Bach J, Krawczyk P, Nico M, Milanowski J. P2.01–44 promoter polymorphisms of TOP2A and ERCC1 genes as predictive factors for chemotherapy in non-small cell lung cancer patients. J Thorac Oncol. 2019;14(10):S656.CrossRef
27.
28.
go back to reference Dong Y, Xiao-Hui L, Wei D, Xin-Jian X, Xi-Yan W. Contribution of DNA repair xeroderma pigmentosum group D genotypes to pancreatic cancer risk in the Chinese Han population. Genet Mol Biol. 2017;41(1):18–26.CrossRef Dong Y, Xiao-Hui L, Wei D, Xin-Jian X, Xi-Yan W. Contribution of DNA repair xeroderma pigmentosum group D genotypes to pancreatic cancer risk in the Chinese Han population. Genet Mol Biol. 2017;41(1):18–26.CrossRef
34.
go back to reference Schillani G, Martinis E, Capozzo MA, Era D, Giraldi T. Psychological response to cancer: role of 5-HTTLPR genetic polymorphism of serotonin transporter. Anticancer Res. 2010;30(9):3823–6.PubMed Schillani G, Martinis E, Capozzo MA, Era D, Giraldi T. Psychological response to cancer: role of 5-HTTLPR genetic polymorphism of serotonin transporter. Anticancer Res. 2010;30(9):3823–6.PubMed
Metadata
Title
Genetic polymorphisms and haplotypes of ERCC1 and ERCC2 associated with quality of life, depression, and anxiety status among patients with lung cancer
Authors
Yunxiang Tang
Ruike Zhang
Yinan Li
Shuyu Xu
Hao Wang
Jingzhou Xu
Lei Xiao
Yajing Wang
Jing Du
Yujia Huang
Tong Su
Publication date
01-12-2021
Publisher
BioMed Central
Published in
BMC Cancer / Issue 1/2021
Electronic ISSN: 1471-2407
DOI
https://doi.org/10.1186/s12885-021-08570-5

Other articles of this Issue 1/2021

BMC Cancer 1/2021 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine