[Effect of lentiviral vector-mediated short hairpin RNA targeting survivin against endometriosis-like lesions in chick embryo chorioallantoic membrane].

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Lentiviral vector-mediated survivin shRNA significantly suppressed angiogenesis and endometriosis lesion formation in a chick embryo model, increasing cell apoptosis and necrosis.

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Abstract

OBJECTIVE: To investigate the inhibitory effect of lentiviral vector-mediated short hairpin RNA targeting survivin (LV-survivin shRNA) on angiogenesis and growth of endometriosis-like lesions in chick en embryo chorioallantoic membrane. METHODS: Eutopic endometrium from women with endometriosis was transplanted onto the non-vascular region of (CAM), where LV-survivin shRNA was delivered subsequently. The angiogenesis and the growth of endometriosis-like lesions in the CAM model were evaluated. RESULTS: The angiogenesis and formation of endometriosis-like lesions were significantly suppressed in the CAM model by treatment with LV-survivin shRNA in comparison with those in the untreated CAM models and models treated with empty LV or DMEM (P<0.001). LV-survivin shRNA also caused a significantly higher cell apoptotic rate in the endometriosis-like lesions than the other treatments (P<0.001) and induced necrosis in the lesions. CONCLUSION: LV-survivin shRNA can effectively inhibit angiogenesis induced by the eutopic endometrium and markedly suppress the formation of endometriosis-like lesions in the CAM model.

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Condition tags

endometriosis

MeSH descriptors

Chorioallantoic Membrane Endometriosis Inhibitor of Apoptosis Proteins Neovascularization, Pathologic RNA, Small Interfering Animals Chick Embryo Chorioallantoic Membrane Disease Models, Animal Endometriosis Female Genetic Vectors Humans Inhibitor of Apoptosis Proteins Lentivirus Lentivirus Neovascularization, Pathologic RNA Interference RNA, Small Interfering Survivin

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europepmc
last seen: 2026-08-08T06:08:32.324769+00:00
openalex
last seen: 2026-06-10T17:14:06.276822+00:00
pubmed
last seen: 2026-05-13T22:16:04.919516+00:00
License: CC0 · commercial use OK