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The Association of Telomere Length with Colorectal Cancer Differs by the Age of Cancer Onset
被引:26
作者:
Boardman, Lisa A.
[1
]
Litzelman, Kristin
[2
]
Seo, Songwon
[3
]
Johnson, Ruth A.
[4
]
Vanderboom, Russell J.
[5
]
Kimmel, Grace W.
[6
]
Cunningham, Julie M.
[4
]
Gangnon, Ronald E.
[7
]
Engelman, Corinne D.
[2
]
Riegert-Johnson, Douglas L.
[1
]
Potter, John
[8
]
Haile, Robert
[9
]
Buchanan, Daniel
[10
]
Jenkins, Mark A.
[11
]
Rider, David N.
[12
]
Thibodeau, Stephen N.
[4
]
Petersen, Gloria M.
[12
]
Skinner, Halcyon G.
[2
]
机构:
[1] Mayo Clin, Coll Med, Dept Gastroenterol & Hepatol, Rochester, MN 55905 USA
[2] Univ Wisconsin, Sch Med & Publ Hlth, Dept Populat Hlth Sci, Madison, WI USA
[3] Korea Inst Radiol & Med Sci, Natl Radiat Emergency Med Ctr, Seoul, South Korea
[4] Mayo Clin, Coll Med, Dept Lab Med & Pathol, Rochester, MN 55905 USA
[5] Mayo Clin, Ctr Canc, Rochester, MN 55905 USA
[6] Univ Michigan, Ann Arbor, MI 48109 USA
[7] Univ Wisconsin, Sch Med & Publ Hlth, Dept Biostat & Med Informat, Madison, WI USA
[8] Fred Hutchinson Canc Res Ctr, Canc Prevent Program, Div Publ Hlth Sci, Seattle, WA 98104 USA
[9] Stanford Canc Inst, Stanford Sch Med, Dept Oncol, Stanford, CA USA
[10] Clive Berghofer Canc Res Ctr, Queensland Inst Med Res, Brisbane, Qld, Australia
[11] Univ Melbourne, Melbourne Sch Populat Hlth, Melbourne, Vic, Australia
[12] Mayo Clin, Coll Med, Dept Hlth Sci Res, Rochester, MN 55905 USA
基金:
美国国家卫生研究院;
关键词:
PREDISPOSITION FACTOR;
QUANTITATIVE PCR;
BLADDER-CANCER;
RISK;
CARCINOMA;
BLOOD;
WOMEN;
SUSCEPTIBILITY;
INSTABILITY;
DYSFUNCTION;
D O I:
10.1038/ctg.2014.3
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
OBJECTIVES: Telomeres are nucleoprotein structures that cap the end of chromosomes and shorten with sequential cell divisions in normal aging. Short telomeres are also implicated in the incidence of many cancers, but the evidence is not conclusive for colorectal cancer (CRC). Therefore, the aim of this study was to assess the association of CRC and telomere length. METHODS: In this case-control study, we measured relative telomere length from peripheral blood leukocytes (PBLs) DNA with quantitative PCR in 598 CRC patients and 2,212 healthy controls. RESULTS: Multivariate analysis indicated that telomere length was associated with risk for CRC, and this association varied in an age-related manner; younger individuals (<= 50 years of age) with longer telomeres (80-99 percentiles) had a 2-6 times higher risk of CRC, while older individuals (>50 years of age) with shortened telomeres (1-10 percentiles) had 2-12 times the risk for CRC. The risk for CRC varies with extremes in telomere length in an age-associated manner. CONCLUSIONS: Younger individuals with longer telomeres or older individuals with shorter telomeres are at higher risk for CRC. These findings indicate that the association of PBL telomere length varies according to the age of cancer onset and that CRC is likely associated with at minimum two different mechanisms of telomere dynamics.
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