TY - JOUR
T1 - Serum levels of insulin-like growth factor I, II, and binding protein 3, transforming growth factor β-1, soluble Fas ligand and superoxide dismutase activity in stomach cancer cases and their controls in the JACC study
AU - Yatsuya, Hiroshi
AU - Toyoshima, Hideaki
AU - Tamakoshi, Koji
AU - Tamakoshi, Akiko
AU - Kondo, Takaaki
AU - Hayakawa, Norihiko
AU - Sakata, Kiyomi
AU - Kikuchi, Shogo
AU - Hoshiyama, Yoshiharu
AU - Fujino, Yoshihisa
AU - Mizoue, Tetsuya
AU - Tokui, Noritaka
AU - Yoshimura, Takesumi
AU - Mori, Mitsuru
AU - Motohashi, Yutaka
AU - Tsuji, Ichiro
AU - Nakamura, Yosikazu
AU - Iso, Hiroyasu
AU - Mikami, Haruo
AU - Inaba, Yutaka
AU - Suzuki, Hiroshi
AU - Shimizu, Hiroyuki
AU - Wakai, Kenji
AU - Tokudome, Shinkan
AU - Ito, Yoshinori
AU - Hashimoto, Shuji
AU - Koizumi, Akio
AU - Kawamura, Takashi
AU - Watanabe, Yoshiyuki
AU - Miki, Tsuneharu
AU - Date, Chigusa
AU - Nose, Takayuki
AU - Shibata, Akira
AU - Okamoto, Naoyuki
AU - Shio, Hideo
AU - Ohno, Yoshiyuki
AU - Kitagawa, Tomoyuki
AU - Kuroki, Toshio
AU - Tajima, Kazuo
PY - 2005
Y1 - 2005
N2 - Background: The prognosis of stomach cancer with advanced stage remains poor. New biomarkers of the disease that may contribute to establish the potential screening strategy would be of value for the early detection of individuals at high risk of the disease. Methods: We conducted a prospective, nested case-control analysis among apparently healthy men and women who were followed for up to 8 years in the Japan Collaborative Cohort (JACC) Study, to evaluate serum levels of insulin-like growth factor I, II, and binding protein 3 (IFG-I, IGF-II, and IGFBP-3), transforming growth factor β-1 (TGF β 1), soluble fas (sFas) and superoxide dismutase activity (SOD) in 210 stomach cancer cases diagnosed in the JACC Study in relation to those levels in their 410 controls. Results: Among 6 serum biomarkers tested for case-control differences, only sFas level in female stomach cancer cases was significantly higher than that of controls (2.22 pg/ml vs. 2.04 pg/mL, respectively; P = 0.013 by two-way analysis of covariance controlling for matching variable). Conclusion: None of the biomarkers consistently predicted future risk of stomach cancer in both men and women in the present analysis. Serum sFas level in women, however, should be studied much more thoroughly whether it provides meaningful refinement of risk stratification, or it elucidate the mechanisms of tumorigenesis in women.
AB - Background: The prognosis of stomach cancer with advanced stage remains poor. New biomarkers of the disease that may contribute to establish the potential screening strategy would be of value for the early detection of individuals at high risk of the disease. Methods: We conducted a prospective, nested case-control analysis among apparently healthy men and women who were followed for up to 8 years in the Japan Collaborative Cohort (JACC) Study, to evaluate serum levels of insulin-like growth factor I, II, and binding protein 3 (IFG-I, IGF-II, and IGFBP-3), transforming growth factor β-1 (TGF β 1), soluble fas (sFas) and superoxide dismutase activity (SOD) in 210 stomach cancer cases diagnosed in the JACC Study in relation to those levels in their 410 controls. Results: Among 6 serum biomarkers tested for case-control differences, only sFas level in female stomach cancer cases was significantly higher than that of controls (2.22 pg/ml vs. 2.04 pg/mL, respectively; P = 0.013 by two-way analysis of covariance controlling for matching variable). Conclusion: None of the biomarkers consistently predicted future risk of stomach cancer in both men and women in the present analysis. Serum sFas level in women, however, should be studied much more thoroughly whether it provides meaningful refinement of risk stratification, or it elucidate the mechanisms of tumorigenesis in women.
UR - http://www.scopus.com/inward/record.url?scp=26244436238&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=26244436238&partnerID=8YFLogxK
U2 - 10.2188/jea.15.S120
DO - 10.2188/jea.15.S120
M3 - Article
C2 - 16127223
AN - SCOPUS:26244436238
SN - 0917-5040
VL - 15
SP - S120-S125
JO - Journal of epidemiology
JF - Journal of epidemiology
IS - SUPPL. 2
ER -