TY - JOUR
T1 - Pre-diagnosis insulin-like growth factor-I and risk of epithelial invasive ovarian cancer by histological subtypes
T2 - A collaborative re-analysis from the Ovarian Cancer Cohort Consortium
AU - Ose, Jennifer
AU - Schock, Helena
AU - Poole, Elizabeth M
AU - Lehtinen, Matti
AU - Visvanathan, Kala
AU - Helzlsouer, Kathy
AU - Buring, Julie E
AU - Lee, I-Min
AU - Tjønneland, Anne
AU - Boutron-Ruault, Marie-Christine
AU - Trichopoulou, Antonia
AU - Mattiello, Amalia
AU - Onland-Moret, N Charlotte
AU - Weiderpass, Elisabete
AU - Sánchez, María-José
AU - Idahl, Annika
AU - Travis, Ruth C
AU - Rinaldi, Sabina
AU - Merritt, Melissa A
AU - Wentzensen, Nicolas
AU - Tworoger, Shelley S
AU - Kaaks, Rudolf
AU - Fortner, Renée T
N1 - Publisher Copyright:
© 2017, Springer International Publishing Switzerland.
PY - 2017/5
Y1 - 2017/5
N2 - PURPOSE: Biologic evidence suggests that the Insulin-like growth factor (IGF)-family may be involved in the etiology of epithelial invasive ovarian cancer (EOC). However, prospective studies investigating the role of IGF-I in ovarian carcinogenesis have yielded conflicting results.METHODS: We pooled and harmonized data from 6 case-control studies nested within the Ovarian Cancer Cohort Consortium to investigate the association between pre-diagnosis IGF-I concentrations and subsequent risk of EOC. We evaluated IGF-I concentrations and risk of EOC overall and by tumor subtype (defined by histology, grade, stage) in 1,270 cases and 2,907 matched controls. Multivariable conditional logistic regression models were used to calculate odds ratios (OR) and 95% confidence intervals (CI).RESULTS: Doubling of IGF-I concentration was associated with significantly lower risk of overall EOC [ORlog2 = 0.82; CI 0.72-0.93]. We observed no heterogeneity by tumor characteristics (e.g., histology, p het = 0.62), menopausal status at blood collection (p het = 0.79), or age at diagnosis (p het = 0.60).CONCLUSIONS: These results suggest that IGF-I concentrations are inversely associated with EOC risk, independent of histological phenotype. Future prospective research should consider potential mechanisms for this association, including, considering other members of the IGF-family to better characterize the role of IGF-signaling in the etiology of EOC.
AB - PURPOSE: Biologic evidence suggests that the Insulin-like growth factor (IGF)-family may be involved in the etiology of epithelial invasive ovarian cancer (EOC). However, prospective studies investigating the role of IGF-I in ovarian carcinogenesis have yielded conflicting results.METHODS: We pooled and harmonized data from 6 case-control studies nested within the Ovarian Cancer Cohort Consortium to investigate the association between pre-diagnosis IGF-I concentrations and subsequent risk of EOC. We evaluated IGF-I concentrations and risk of EOC overall and by tumor subtype (defined by histology, grade, stage) in 1,270 cases and 2,907 matched controls. Multivariable conditional logistic regression models were used to calculate odds ratios (OR) and 95% confidence intervals (CI).RESULTS: Doubling of IGF-I concentration was associated with significantly lower risk of overall EOC [ORlog2 = 0.82; CI 0.72-0.93]. We observed no heterogeneity by tumor characteristics (e.g., histology, p het = 0.62), menopausal status at blood collection (p het = 0.79), or age at diagnosis (p het = 0.60).CONCLUSIONS: These results suggest that IGF-I concentrations are inversely associated with EOC risk, independent of histological phenotype. Future prospective research should consider potential mechanisms for this association, including, considering other members of the IGF-family to better characterize the role of IGF-signaling in the etiology of EOC.
KW - Developmental pathways
KW - Epithelial ovarian cancer
KW - Histological subtypes
KW - IGF-I
KW - Developmental pathways
UR - http://www.scopus.com/inward/record.url?scp=85012897957&partnerID=8YFLogxK
U2 - 10.1007/s10552-017-0852-8
DO - 10.1007/s10552-017-0852-8
M3 - Article
C2 - 28205047
SN - 0957-5243
VL - 28
SP - 429
EP - 435
JO - Cancer Causes & Control
JF - Cancer Causes & Control
IS - 5
ER -