Abstract |
Tannic acid (TA) has been associated with anticancer functions in multiple tumor types both in vitro and in vivo. However, its effect on ovarian carcinoma cells has not been investigated, and its underlying anticancer mechanism(s) remain unclear. In this study, the effects of TA alone and in combination with cisplatin were evaluated using ovarian carcinoma cell lines. Combined treatment with TA and cisplatin was found to induce apoptosis and increase DNA damage in the cisplatin-resistant (SKOV-3 CDDP/R) and cisplatin-sensitive (SKOV-3) human ovarian carcinoma cell lines, respectively. TA was also found to enhance the toxicity of cisplatin in ovarian carcinoma cells associated with the inhibition of poly(ADP-ribose) glycohydrolase (PARG) expression, increase the accumulation of poly(ADP-ribose) (pADPr), following the release of apoptosis-inducing factor, and the activation of caspase-3. In conclusion, as a PARG inhibitor, TA showed anticancer activity and increased the sensitivity of SKOV-3 cells and SKOV-3 CDDP/R cell lines to cisplatin.
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Authors | Yanyan Sun, Tianhua Zhang, Beidi Wang, Hulun Li, Peiling Li |
Journal | Anti-cancer drugs
(Anticancer Drugs)
Vol. 23
Issue 9
Pg. 979-90
(Oct 2012)
ISSN: 1473-5741 [Electronic] England |
PMID | 22785358
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antineoplastic Agents
- Tannins
- Glycoside Hydrolases
- poly ADP-ribose glycohydrolase
- Cisplatin
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Topics |
- Antineoplastic Agents
(pharmacology)
- Apoptosis
(drug effects)
- Cell Culture Techniques
- Cell Line, Tumor
- Cell Survival
(drug effects)
- Cisplatin
(pharmacology)
- DNA Damage
- Drug Resistance, Neoplasm
(drug effects)
- Drug Synergism
- Female
- Flow Cytometry
- Glycoside Hydrolases
(antagonists & inhibitors)
- Humans
- Microscopy, Fluorescence
- Ovarian Neoplasms
(enzymology, pathology)
- Tannins
(pharmacology)
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