GWAS-identified telomere length associated genetic variants predict risk of recurrence of HPV-positive oropharyngeal cancer after definitive radiotherapy

被引:1
|
作者
Sun, Peng [1 ,2 ]
Wei, Peng [3 ]
Liu, Hongliang [4 ]
Wu, Jia [5 ]
Gross, Neil D. [1 ]
Sikora, Andrew G. [1 ]
Wei, Qingyi [4 ]
Shete, Sanjay [5 ]
Zafereo, Mark E.
Liu, Jisheng [2 ]
Li, Guojun [1 ,6 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Head & Neck Surg, 1515 Holcombe Blvd,Unit 1445, Houston, TX 77030 USA
[2] Soochow Univ, Dept Otolaryngol, Affiliated Hosp 1, Suzhou 215006, Peoples R China
[3] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[4] Duke Univ, Sch Med, Dept Med, Durham, NC 27710 USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Imaging Phys, Houston, TX 77030 USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Epidemiol, Houston, TX 77030 USA
来源
EBIOMEDICINE | 2023年 / 94卷
关键词
Telomere length; Recurrence; Genetic variant; Polymorphism; Biomarkers; Human papillomavirus; Oropharyngeal cancer; GENOME-WIDE ASSOCIATION; SQUAMOUS-CELL CARCINOMA; TERT PROMOTER; NECK-CANCER; HEAD; CHEMOTHERAPY; RADIATION; BREAST; LOCI; AGE;
D O I
10.1016/j.ebiom.2023.104722
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Lymphocyte telomere length (LTL)-related genetic variants may modulate LTL and affect recurrence of squamous cell carcinoma of the oropharynx (SCCOP).Methods A total of 1013 patients with incident SCCOP were recruited and genotyped for 16 genome-wide association study (GWAS)-identified TL-related polymorphisms. Of these patients, 489 had tumour HPV16 status determination. Univariate and multivariate analyses were performed to evaluate associations.Findings Of the 16 TL-related polymorphisms, four were significantly associated with LTL: rs1920116, rs3027234, rs6772228, and rs11125529, and the patients with putatively favourable genotypes had approximately 1.5-3 times the likelihood of shorter LTL compared with patients with the corresponding risk genotypes. Moreover, patients with one to four favourable genotypes of the four combined polymorphisms had approximately 3-11 times the likelihood of shorter LTL compared with patients with no favourable genotype. The four LTL-related polymorphisms were significantly associated with approximately 40% reduced risk (for favourable genotypes) or doubled risk (for risk genotypes) of recurrence, and similar but more pronounced associations were observed in patients with tumour HPV16-positive SCCOP. Similarly, patients with one to four risk genotypes had significantly approximately 2.5-4 times increased recurrence risk compared with patients with no risk genotype, and similar but more pronounced associations were observed in patients with tumour HPV16-positive SCCOP.Interpretation Four LTL-related polymorphisms individually or jointly modify LTL and risk of recurrence of SCCOP, particularly HPV-positive SCCOP. These LTL-related polymorphisms could have potential to further stratify patients with HPV-positive SCCOP for individualized treatment and better survival.
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页数:14
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