TY - JOUR
T1 - Association of the transforming growth factor β1 promoter polymorphism, C-509T, with smoking status and survival in advanced non-small cell lung cancer
AU - Togashi, Yosuke
AU - Masago, Katsuhiro
AU - Fujita, Shiro
AU - Kim, Young Hak
AU - Sakamori, Yuichi
AU - Hatachi, Yukimasa
AU - Fukuhara, Akiko
AU - Nagai, Hiroki
AU - Mio, Tadashi
AU - Mishima, Michiaki
PY - 2011/2
Y1 - 2011/2
N2 - Transforming growth factor β (TGF-β) signaling can inhibit tumor growth in developing tumors. However, it promotes tumor invasiveness and metastasis in late-stage tumors. A number of TGF-β gene polymorphisms have been identified that can affect the survival of patients with advanced non-small cell lung cancer (NSCLC). In this study, we investigated the association of the TGF-β1 polymorphism, C-509T, with survival in patients with advanced NSCLC. Japanese patients who were treated for unresectable advanced NSCLC between April 2003 and March 2008 at Kyoto University Hospital, were enrolled in this study. Analyses of genotype associations with survival outcomes were performed using statistical tests. The median survival of patients with the TT genotype was shorter, although not significantly, than that of patients with either the CT or CC genotype. Based on both univariable and multivariable analyses, the TGF-β1 polymorphism, C-509T, was not associated with prognosis. In patients with a smoking status of <40 pack-years, the median survival was significantly shorter with the TT genotype than with the CT or CC genotype. Based on univariable analysis, stage IV cancer and the TT genotype had a significant prognostic effect on survival. Based on multivariable analysis, the TT genotype was a significantly independent prognostic factor for survival. There was no association between the TGF-β1 polymorphism, C-509T, and survival in patients with advanced NSCLC. In patients with a smoking status of <40 pack-years, however, the TGF-β1 polymorphism, C-509T, was significantly associated with the prognosis of advanced NSCLC, and the TT genotype was an independent prognostic factor for poor survival.
AB - Transforming growth factor β (TGF-β) signaling can inhibit tumor growth in developing tumors. However, it promotes tumor invasiveness and metastasis in late-stage tumors. A number of TGF-β gene polymorphisms have been identified that can affect the survival of patients with advanced non-small cell lung cancer (NSCLC). In this study, we investigated the association of the TGF-β1 polymorphism, C-509T, with survival in patients with advanced NSCLC. Japanese patients who were treated for unresectable advanced NSCLC between April 2003 and March 2008 at Kyoto University Hospital, were enrolled in this study. Analyses of genotype associations with survival outcomes were performed using statistical tests. The median survival of patients with the TT genotype was shorter, although not significantly, than that of patients with either the CT or CC genotype. Based on both univariable and multivariable analyses, the TGF-β1 polymorphism, C-509T, was not associated with prognosis. In patients with a smoking status of <40 pack-years, the median survival was significantly shorter with the TT genotype than with the CT or CC genotype. Based on univariable analysis, stage IV cancer and the TT genotype had a significant prognostic effect on survival. Based on multivariable analysis, the TT genotype was a significantly independent prognostic factor for survival. There was no association between the TGF-β1 polymorphism, C-509T, and survival in patients with advanced NSCLC. In patients with a smoking status of <40 pack-years, however, the TGF-β1 polymorphism, C-509T, was significantly associated with the prognosis of advanced NSCLC, and the TT genotype was an independent prognostic factor for poor survival.
KW - Cigarette smoking
KW - Non-small cell lung cancer
KW - Single nucleotide polymorphism
KW - Survival
KW - Transforming growth factor β1
UR - http://www.scopus.com/inward/record.url?scp=78651370431&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=78651370431&partnerID=8YFLogxK
U2 - 10.3892/or.2010.1098
DO - 10.3892/or.2010.1098
M3 - Article
C2 - 21165571
AN - SCOPUS:78651370431
SN - 1021-335X
VL - 25
SP - 377
EP - 382
JO - Oncology reports
JF - Oncology reports
IS - 2
ER -