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Fig. 7 | Journal of Translational Medicine

Fig. 7

From: Irradiation-responsive PRDM10-DT modulates the angiogenic response in human NSCLC cells in an SP1-dependent manner via the miR-663a/TGF-β1 axis

Fig. 7

Mechanistic model of X-ray irradiation-induced tumor angiogenesis through PRDM10-DT/miR-663a/TGF-β1 axis that activated by SP1 in lung adenocarcinoma cells. Radiation activates SP1 binding to PRDM10-DT promoter region and enhances the transcription of PRDM10-DT. Up-regulated PRDM10-DT competitively binds miR-663a and then promotes TGF-β1 and VEGF expression and facilitates tumor angiogenesis

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