Title : Prevention of Prostate Cancer with Oleanane Synthetic Triterpenoid CDDO-Me in the TRAMP Mouse Model of Prostate Cancer.

Pub. Date : 2011

PMID : 21961053






4 Functional Relationships(s)
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1 CDDO-Me inhibited the growth of murine TRAMPC-1 prostate cancer cells by inducing apoptosis through the inhibition of antiapoptotic p-Akt, p-mTOR and NF-kappaB. bardoxolone methyl thymoma viral proto-oncogene 1 Mus musculus
2 Treatment with CDDO-Me inhibited the expression of prosurvival p-Akt and NF-kappaB in the prostate and knocking-down Akt in TRAMPC-1 tumor cells sensitized them to CDDO-Me. bardoxolone methyl thymoma viral proto-oncogene 1 Mus musculus
3 Treatment with CDDO-Me inhibited the expression of prosurvival p-Akt and NF-kappaB in the prostate and knocking-down Akt in TRAMPC-1 tumor cells sensitized them to CDDO-Me. bardoxolone methyl thymoma viral proto-oncogene 1 Mus musculus
4 These findings indicated that Akt is a target for apoptoxicity in TRAMPC-1 cells in vitro and potentially a target of CDDO-Me for inhibition of prostate cancer in vivo. bardoxolone methyl thymoma viral proto-oncogene 1 Mus musculus