Title : Enhancement of the effects of gemcitabine against pancreatic cancer by oridonin via the mitochondrial caspase-dependent signaling pathway.

Pub. Date : 2014 Dec

PMID : 25242370






5 Functional Relationships(s)
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1 Western blot and quantitative polymerase chain reaction analyses demonstrated that the expression levels of the anti-apoptotic gene Bcl-2 and the Bcl-2/Bax ratio in the oridonin and the oridonin plus gemcitabine groups were significantly downregulated as compared with the gemcitabine treatment and control groups. gemcitabine BCL2 associated X, apoptosis regulator Homo sapiens
2 The results suggested that oridonin improved the anti-tumor effects of gemcitabine through the enhancement of gemcitabine-induced apoptosis.This mechanism may be through the downregulation of Bcl-2 expression and the upregulation of Bax expression, resulting in the reduction of the Bcl-2/Bax ratio. gemcitabine BCL2 associated X, apoptosis regulator Homo sapiens
3 The results suggested that oridonin improved the anti-tumor effects of gemcitabine through the enhancement of gemcitabine-induced apoptosis.This mechanism may be through the downregulation of Bcl-2 expression and the upregulation of Bax expression, resulting in the reduction of the Bcl-2/Bax ratio. gemcitabine BCL2 associated X, apoptosis regulator Homo sapiens
4 The results suggested that oridonin improved the anti-tumor effects of gemcitabine through the enhancement of gemcitabine-induced apoptosis.This mechanism may be through the downregulation of Bcl-2 expression and the upregulation of Bax expression, resulting in the reduction of the Bcl-2/Bax ratio. gemcitabine BCL2 associated X, apoptosis regulator Homo sapiens
5 The results suggested that oridonin improved the anti-tumor effects of gemcitabine through the enhancement of gemcitabine-induced apoptosis.This mechanism may be through the downregulation of Bcl-2 expression and the upregulation of Bax expression, resulting in the reduction of the Bcl-2/Bax ratio. gemcitabine BCL2 associated X, apoptosis regulator Homo sapiens