1α,25(OH)2D3 Analog, MART-10, Inhibits Neuroendocrine Tumor Cell Metastasis After VEGF-A Stimulation

被引:8
作者
Chiang, Kun-Chun [1 ,2 ]
Yeh, Chun-Nan [5 ]
Pang, Jong-Hwei S. [6 ]
Hsu, Jun-Te [5 ]
Yeh, Ta-Sen [5 ]
Chen, Li-Wei [3 ]
Kuo, Sheng-Fong [4 ]
Takano, Masashi [8 ]
Chen, Tai C. [9 ]
Kittaka, Atsushi [8 ]
Hsieh, Po-Jen [3 ]
Juang, Horng-Heng [7 ]
机构
[1] Chang Gung Univ, Chang Gung Mem Hosp, Dept Gen Surg, Keelung, Taiwan
[2] Chang Gung Univ, Chang Gung Mem Hosp, Zebrafish Ctr, Keelung, Taiwan
[3] Chang Gung Univ, Dept Gastroenterol, Chang Gung Mem Hosp, Keelung, Taiwan
[4] Chang Gung Univ, Chang Gung Mem Hosp, Dept Endocrinol & Metab, Keelung, Taiwan
[5] Chang Gung Univ, Chang Gung Mem Hosp, Dept Gen Surg, Taoyuan, Taiwan
[6] Chang Gung Univ, Grad Inst Clin Med Sci, Taoyuan, Taiwan
[7] Chang Gung Univ, Dept Anat, Coll Med, Taoyuan, Taiwan
[8] Teikyo Univ, Fac Pharmaceut Sci, Sagamihara, Kanagawa, Japan
[9] Boston Univ, Sch Med, Endocrine Lab, Boston, MA 02118 USA
关键词
PanNET; MART-10; vitamin D; EMT; 1; alpha; 25(OH)(2)D-3; metastasis; VEGF-A; ENDOTHELIAL GROWTH-FACTOR; VITAMIN-D ANALOG; HUMAN PANCREATIC-CANCER; PHASE-II; IN-VITRO; EXPRESSION; DISEASE; SNAIL; NEUROPILIN-1; PROGRESSION;
D O I
10.21873/anticanres.12072
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aims: Pancreatic neuroendocrine tumors (PanNETs) are usually diagnosed in an advanced stage. Most patients with PanNETs die of metastasis. Vascular endothelial growth factor-A (VEGF-A) is a strong stimulator of angiogenesis and tumor metastasis. We aimed to investigate the effect of MART-10 [19-nor-2 alpha-(3-hydroxypropyl)-1 alpha, 25(OH)(2)D-3], a 1 alpha, 25-dihydroxy-vitamin D3 (1 alpha,25(OH)(2)D-3) analog, on PanNET cell metastasis after VEGF-A stimulation. Materials and Methods: Migration and invasion assays, western blot, and immunofluorescent staining were applied in this study. Results: VEGF-A increased PanNET cell migration and invasion, which was attenuated by 1 alpha,25(OH)(2)D-3 and MART-10. VEGF-A treatment stimulated epithelial-mesenchymal transition (EMT) of PanNET cells. During this process, expression of snail family transcriptional repressor 1 and 2, and fibronectin was up-regulated. 1 alpha,25(OH)(2)D-3 and MART-10 counteracted VEGF-A-induced EMT. In addition, expression of neuropilin 1, a key protein in VEGF-A signaling, was down-regulated by 1 alpha,25(OH)(2)D-3 and MART-10. Furthermore, synthesis of F-actin was increased by VEGF-A and reduced by 1 alpha,25(OH)(2)D-3 and MART-10. Conclusion: Our data indicate that MART-10 could be deemed a promising drug for PanNET treatment.
引用
收藏
页码:6215 / 6221
页数:7
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