Acta Pharmaceutica, Vol. 69 No. 3, 2019.
Short communication, Note
https://doi.org/10.2478/acph-2019-0021
Inhibitory effect of taspine derivative TAD1822-7 on tumor cell growth and angiogenesis via suppression of EphrinB2 and related signaling pathways
RUI LIU
; School of Pharmacy, Xi'an Jiaotong University, 710061 Xi'an, Shaanxi, China
RUNZE YU
; School of Pharmacy, Xi'an Jiaotong University, 710061 Xi'an, Shaanxi, China
YUXIN CUI
; School of Pharmacy, Xi'an Jiaotong University, 710061 Xi'an, Shaanxi, China
MENGYING FAN
; School of Pharmacy, Xi'an Jiaotong University, 710061 Xi'an, Shaanxi, China
BO WANG
; School of Pharmacy, Xi'an Jiaotong University, 710061 Xi'an, Shaanxi, China
YANMIN ZHANG
; School of Pharmacy, Xi'an Jiaotong University, 710061 Xi'an, Shaanxi, China
Abstract
The aim of this study was to investigate the inhibitory effect of TAD1822-7, a synthesized taspine derivative, on cancer through its effects on tumor cell growth and angiogenesis via suppression of EphrinB2. The obtained data showed that TAD1822-7 decreased Bel-7402 cell viability and colony formation ability and suppressed cell migration. TAD1822-7 effectively inhibited blood vessel formation in an aortic ring assay to examine angiogenesis. Moreover, it also downregulated the expression of VEGFR2, VEGFR3, CD34, PLCγ, Akt, MMP2, MMP9, and CXCR4, and suppressed the expression of EphrinB2 and its PDZ protein, PICK1, in Bel-7402 cells. These results indicate that TAD1822-7 is a potential anti-angiogenic agent that can inhibit the viability and migration of Bel-7402 cells via suppression of EphrinB2 and the related signaling pathways.
Keywords
TAD1822-7; EphrinB2; Bel-7402 cells; proliferation; migration; anti-angiogenesis
Hrčak ID:
216138
URI
Publication date:
30.9.2019.
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