Expression of the obesity hormone leptin and its receptor correlates with hypoxia-inducible factor-1α in human colorectal cancer

被引:40
|
作者
Koda, M.
Sulkowska, M.
Kanczuga-Koda, L.
Cascio, S.
Colucci, G.
Russo, A.
Surmacz, E.
Sulkowski, S.
机构
[1] Med Univ Bialystok, Dept Pathomorphol, PL-15269 Bialystok, Poland
[2] Temple Univ, Sbarro Inst Canc Res & Mol Med, Philadelphia, PA 19122 USA
[3] Univ Palermo, Dept Surg & Oncol, Sect Med Oncol, Palermo, Italy
[4] Natl Inst Oncol, Div Med Oncol, Bari, Italy
关键词
colorectal cancer; hypoxia-inducible factor-1 alpha; leptin; leptin receptor; obesity;
D O I
10.1093/annonc/mdm238
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The obesity hormone, leptin, has been found to play a role in development and proliferation of normal and malignant tissues. Leptin activity is mediated through the leptin receptor (ObR) that is often expressed in different human cancer cells. Previously, we found that the expression of leptin and ObR can be stimulated by hypoxia-mimetic agents. The aim of this study was to analyze the abundance of and relationships among leptin, ObR and hypoxia-inducible factor-1 alpha (HIF-1 alpha, transcriptional regulator) in human colorectal cancer. Materials and methods: We investigated the expression of leptin, ObR and HIF-1 alpha. in colorectal cancer specimens from 135 patients who underwent curative resection. Results: Immunoreactivity for leptin, ObR and HIF-1 alpha protein was observed in 69 of 135 (51.1%), 129 of 135 (95.5%) and 88 of 135 (65.2%) of colorectal cancers, respectively. Statistically significant positive correlations were noted between leptin and HIF-1 alpha (P = 0.005, r = 0.243), ObR and HIF-1 alpha (P < 0.001, r = 0.325) as well as leptin and ObR (P < 0.001, r = 0.426) in the group of all patients as well as in various subgroups depending on clinicopathological features. Conclusions: The results indicate that the leptin system is overexpressed in human colorectal cancer and this overexpression appears to be associated with the abundance of HIF-1 alpha.
引用
收藏
页码:116 / 119
页数:4
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