Expression of Angiogenic Regulators, VEGF and Leptin, Is Regulated by the EGF/PI3K/STAT3 Pathway in Colorectal Cancer Cells

被引:40
作者
Cascio, Sandra [1 ]
Ferla, Rita [1 ,2 ]
D'Andrea, Aleco [1 ]
Gerbino, Aldo [3 ]
Bazan, Viviana [1 ]
Surmacz, Eva [2 ]
Russo, Antonio [1 ]
机构
[1] Univ Palermo, Dept Surg & Oncol Sci, Sect Med Oncol, I-90127 Palermo, Italy
[2] Temple Univ, Sbarro Inst Canc Res & Mol Med, Philadelphia, PA 19122 USA
[3] Univ Palermo, Dept Expt Med, Inst Pathol, Histol & Embriol Sect, I-90127 Palermo, Italy
关键词
ENDOTHELIAL GROWTH-FACTOR; HUMAN GLIOBLASTOMA CELLS; TUMOR ANGIOGENESIS; FACTOR RECEPTOR; SIGNAL TRANSDUCERS; COLON-CANCER; HYPOXIA; STAT3; ACTIVATION; PROMOTES;
D O I
10.1002/jcp.21843
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Both leptin and vascular endothelial growth factor (VEGF) are growth and angiogenic cytokines that are upregulated in different types of cancer and have been implicated in neoplastic progression. Here we investigated the molecular mechanism by which leptin and VEGF expression are regulated in colon cancer by epidermal growth factor (EGF). In colon cancer cell line HT-29, EGF induced the binding of signal transducer and activator transcription 3 (STAT3) to STAT3 consensus motifs within the VEGF and leptin promoters and stimulated leptin and VEGF mRNA and protein synthesis. All these EGF effects were significantly blocked when HT-29 cells were treated with an inhibitor of the phosphoinositide 3-kinase (PI3K) pathway, LY294002, or with small interfering RNA (siRNA) targeting STAT3. Thus, our study identified the EGF/PI3K/STAT3 signaling as an essential pathway regulating VEGF and leptin expression in EGF-responsive colon cancer cells. This suggests that STAT3 pathways might constitute attractive pharmaceutical targets in colon cancer patients where anti-EGF receptor drugs are ineffective. J. Cell. Physiol. 221: 189-194, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:189 / 194
页数:6
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