TY - JOUR
T1 - Leukocyte Telomere Length and Pancreatic Cancer Risk
T2 - Updated Epidemiologic Review
AU - Antwi, Samuel O.
AU - Petersen, Gloria M.
N1 - Funding Information:
From the *Division of Epidemiology, Department of Health Sciences Research, Mayo Clinic, Jacksonville, FL; and †Division of Epidemiology, Department of Health Sciences Research, Mayo Clinic, Rochester, MN. Received for publication June 7, 2017; accepted December 15, 2017. Address correspondence to: Samuel O. Antwi, PhD, Mayo Clinic, 4500 San Pablo Road, S. Vincent Stabile Building, North, 756 N, Jacksonville, FL 32224 (e‐mail: antwi.samuel@mayo.edu). This research was supported by a National Cancer Institute Specialized Program of Research Excellence in Pancreatic Cancer grant (P50 CA102701) and another National Cancer Institute grant (R25 CA92049). The authors declare no conflict of interest. Copyright © 2018 Wolters Kluwer Health, Inc. All rights reserved. DOI: 10.1097/MPA.0000000000000995
Publisher Copyright:
© 2018 Wolters Kluwer Health, Inc. All rights reserved.
PY - 2018/3/1
Y1 - 2018/3/1
N2 - Many risk factors have been firmly established for pancreatic cancer (PC), but the molecular processes by which known risk factors influence susceptibility to PC are not clear. There has been a recent upsurge of interest in the role of telomere length (TL), the protective DNA sequence repeats at chromosome ends, in pancreatic carcinogenesis. Given this heightened interest, we performed an in-depth, focused, and up-to-date review of the epidemiological evidence linking leukocyte TL (LTL) with PC risk. We searched MEDLINE, Embase, and the Cochrane Library databases for all published studies on LTL and PC risk, up to May 2017. Five studies were identified for review: 4 nested case-control studies and 1 retrospective case-control study. Two studies found opposite associations between LTL and PC risk: 1 found a dose-response positive association and the other found a dose-response inverse association. Two studies also found a "U-shaped" association, whereas another reported a weak nonlinear relationship. We offer potential reasons for the conflicting findings including variation in study design, biospecimen characteristics, and differences in interlaboratory measurements of TL. Future studies should carefully control for risk factors of PC that are associated also with telomere attrition and investigate the role of genetic variation in TL maintenance.
AB - Many risk factors have been firmly established for pancreatic cancer (PC), but the molecular processes by which known risk factors influence susceptibility to PC are not clear. There has been a recent upsurge of interest in the role of telomere length (TL), the protective DNA sequence repeats at chromosome ends, in pancreatic carcinogenesis. Given this heightened interest, we performed an in-depth, focused, and up-to-date review of the epidemiological evidence linking leukocyte TL (LTL) with PC risk. We searched MEDLINE, Embase, and the Cochrane Library databases for all published studies on LTL and PC risk, up to May 2017. Five studies were identified for review: 4 nested case-control studies and 1 retrospective case-control study. Two studies found opposite associations between LTL and PC risk: 1 found a dose-response positive association and the other found a dose-response inverse association. Two studies also found a "U-shaped" association, whereas another reported a weak nonlinear relationship. We offer potential reasons for the conflicting findings including variation in study design, biospecimen characteristics, and differences in interlaboratory measurements of TL. Future studies should carefully control for risk factors of PC that are associated also with telomere attrition and investigate the role of genetic variation in TL maintenance.
KW - Pancreatic adenocarcinoma
KW - Pancreatic cancer
KW - Telomere genes
KW - Telomere length
KW - Telomeres
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U2 - 10.1097/MPA.0000000000000995
DO - 10.1097/MPA.0000000000000995
M3 - Review article
C2 - 29424808
AN - SCOPUS:85042532642
SN - 0885-3177
VL - 47
SP - 265
EP - 271
JO - Pancreas
JF - Pancreas
IS - 3
ER -