Telomere length variation: A potential new telomere biomarker for lung cancer risk

被引:19
|
作者
Sun, Bing [1 ]
Wang, Ying [1 ]
Kota, Krishna [1 ]
Shi, Yaru [1 ]
Motlak, Salaam [1 ]
Makambi, Kepher [1 ,2 ]
Loffredo, Christopher A. [1 ,2 ]
Shields, Peter G. [3 ]
Yang, Qin [4 ]
Harris, Curtis C. [5 ]
Zheng, Yun-Ling [1 ]
机构
[1] Georgetown Univ, Med Ctr, Lombardi Comprehens Canc Ctr, Canc Prevent & Control Program, Washington, DC 20057 USA
[2] Georgetown Univ, Med Ctr, Dept Biostat Bioinformat & Biomath, Washington, DC 20057 USA
[3] Ohio State Univ, Wexner Med Ctr, James Canc Hosp, Columbus, OH 43220 USA
[4] Washington Univ, Sch Med, Dept Radiat Oncol, Div Canc Biol, St Louis, MO USA
[5] NCI, Human Carcinogenesis Lab, Ctr Canc Res, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
Lung cancer; Telomere length variation; Telomere length; Blood-based biomarker; Risk prediction; Telomere dysfunction; HEMATOPOIETIC STEM-CELLS; OXIDATIVE STRESS; DYSKERATOSIS-CONGENITA; CHROMOSOME STABILITY; HUMAN FIBROBLASTS; DNA-DAMAGE; DYSFUNCTION; SENESCENCE; MICE; AGE;
D O I
10.1016/j.lungcan.2015.03.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: In this report the associations between telomere length variation (TLV), mean telomere length in blood lymphocytes and lung cancer risk were examined. Materials and methods: The study design is case-control. Cases (N = 191) were patients newly diagnosed with histologically confirmed non-small cell lung cancer. Controls (N = 207) were healthy individuals recruited from the same counties as cases and matched to cases on age and gender. Telomere fluorescent in situ hybridization was used to measure telomere features using short-term cultured blood lymphocytes. Logistic regression was used to estimate the strength of association between telomere features and lung cancer risk. Results: Telomere length variation across all chromosomal ends was significantly associated with lung cancer risk; adjusted odds ratios 4.67 [95% confidence interval (CI): 1.46-14.9] and 0.46 (95% CI: 025-0.84) for younger (age <= 60) and older (age >60) individuals, respectively. TLV and mean telomere length jointly affected lung cancer risk: when comparing individuals with short telomere length and high TLV to those with long telomere length and low TLV, adjusted odd ratios were 8.21 (95% Cl: 1.71-39.5) and 0.33 (95% CI: 0.15-0.72) for younger and older individuals, respectively. Conclusions: TLV in blood lymphocytes is significantly associated with lung cancer risk and the associations were modulated by age. TLV in combination with mean telomere length might be useful in identifying high risk population for lung cancer computerized tomography screening. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:297 / 303
页数:7
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