Telomere dysfunction: a potential cancer predisposition factor. J Natl Cancer Inst 2003;95:1211–1218

Background: Genetic instability associated with telomere dysfunction (i.e., short telomeres) is an early event in tumori-genesis. We investigated the association between telomere length and cancer risk in four ongoing case–control studies. Methods: All studies had equal numbers of case patients and matched control subjects (92 for head and neck cancer, 135 for bladder cancer, 54 for lung cancer, and 32 for renal cell carcinoma). Telomere length was measured in peripheral blood lymphocytes from study participants. Genetic insta-bility was assessed with the comet assay. Patient and disease characteristics were collected and analyzed for associations with risk for these cancers. All statistical tests were two-sided. Results: Telomeres were statistically significantly shorter in patients with head and neck cancer (6.5 kilobases [kb]) than in control subjects (7.4 kb) (difference = 0.9 kb, 95 % confidence interval [CI] = 0.5 to 1.2 kb; P<.001). Nine percent of patients with head and neck cancer were in the longest quartile of telomere length, whereas 59 % were in the shortest quartile. Similar patterns were observed for lung, renal cell, and bladder cancer. When subjects were catego-rized into telomere length quartiles defined by the distribu-tion in control subjects, the following inverse relationship between telomere length and cancer risk was observed: ad-justed odds ratios [ORs] for decreasing quartiles = 0.84 (95 % CI = 0.36 to 1.97), 1.77 (95 % CI = 0.72 to 4.36), and 5.11 (95 % CI = 1.90 to 13.77). In stratified analysis, we found a suggestive greater-than-additive interaction between smoking status and telomere length: for ever smokers with short telomeres, OR = 25.05 (95 % CI = 6.91 to 90.73); for never smokers with short telomeres, OR = 6.18 (95 % CI = 1.72 to 22.13); and for ever smokers with long telomeres, OR = 6.49 (95 % CI = 1.54 to 27.38). Telomere length was sta-tistically significantly and inversely associated with baseline and mutagen-induced genetic instability. Conclusion: Short telomeres appear to be associated with increased risks for human bladder, head and neck, lung, and renal cell cancers