Caspase 3 in dying tumor cells mediates post-irradiation angiogenesis.

Journal Article (Journal Article)

Cytotoxic radiotherapy unfavorably induces tumor cells to generate various proangiogenic substances, promoting post-irradiation angiogenesis (PIA), which is one of major causes of radiotherapy failure. Though several studies have reported some mechanisms behind PIA, they have not yet described the beginning proangiogenic motivator buried in the irradiated microenvironment. In this work, we revealed that dying tumor cells induced by irradiation prompted PIA via a caspase 3 dependent mechanism. Proteolytic inactivation of caspase 3 in dying tumor cells by transducing a dominant-negative version weakened proangiogenic effects in vitro and in vivo. In addition, inhibition of caspase 3 activity suppressed tumor angiogenesis and tumorigenesis in xenograft mouse model. Importantly, we identified vascular endothelial growth factor (VEGF)-A as a downstream proangiogenic factor regulated by caspase 3 possibly through Akt signaling. Collectively, these findings indicated that besides acting as a key executioner in apoptosis, caspase 3 in dying tumor cells may play a central role in driving proangiogenic response after irradiation. Thus, radiotherapy in combination with caspase 3 inhibitors may be a novel promising therapeutic strategy to reduce tumor recurrence due to restrained PIA.

Full Text

Duke Authors

Cited Authors

  • Feng, X; Tian, L; Zhang, Z; Yu, Y; Cheng, J; Gong, Y; Li, C-Y; Huang, Q

Published Date

  • October 20, 2015

Published In

Volume / Issue

  • 6 / 32

Start / End Page

  • 32353 - 32367

PubMed ID

  • 26431328

Pubmed Central ID

  • PMC4741698

Electronic International Standard Serial Number (EISSN)

  • 1949-2553

Digital Object Identifier (DOI)

  • 10.18632/oncotarget.5898


  • eng

Conference Location

  • United States