We previously reported that prenylated chalcone 2 (PC2), the O-prenyl derivative (2) of 2′-hydroxy-3,4,4′,5,6′-pentamethoxychalcone (1), induced cytotoxicity of tumor cells via disruption of p53-MDM2 interaction. However, the cellular changes through which PC2 exerts its cytotoxic activity and its antitumor potential, remain to be addressed. In the present work, we aimed to (i) characterize the effect of PC2 on mitotic progression and the underlying mechanism; and to (ii) explore this information to evaluate its ability to sensitize tumor cells to paclitaxel in a combination regimen. PC2 was able to arrest breast adenocarcinoma MCF-7 and non-small cell lung cancer NCI-H460 cells in mitosis. All mitosis-arrested cells showed collapsed mitoti...
Resistance to some cancer chemotherapeutic drugs has been identifed. One strategy to overcome that p...
© 2016 by the authors; licensee MDPI, Basel, Switzerland. Hepatocellular carcinoma (HCC) is one of t...
In the present study, we investigated the in vitro antitumor functions of a synthetic chalcone deriv...
We previously reported that prenylated chalcone 2 (PC2), the O-prenyl derivative (2) of 2′-hydroxy-3...
We previously reported that prenylated chalcone 2 (PC2), the O-prenyl derivative (2) of 2'-hydroxy-3...
We previously reported that prenylated chalcone 2 (PC2), the O-prenyl derivative (2) of 2′-hydroxy-3...
Aim Chalcones are naturally occurring compounds with recognized anticancer activity. It was recently...
The p53 protein is one of the most important tumor suppressors that are frequently inactivated in ca...
Naturally-occurring chalcones and synthetic chalcone analogues have been demonstrated to have many b...
[[abstract]]Combination of selecting agents that act on different cellular mechanisms is a common st...
[[abstract]]Paclitaxel is a potential cancer chemotherapeutic agent for ovary, breast, and head and ...
The taxanes are effective microtubule-stabilizing chemotherapy drugs that inhibit mitosis, induce ap...
Chalcones are valuable structures for drug discovery due to their broad bioactivity spectrum. In thi...
International audienceChalcones are naturally occurring compounds with diverse pharmacological activ...
Naturally-occurring chalcones and synthetic chalcone analogues have been demonstrated to have many b...
Resistance to some cancer chemotherapeutic drugs has been identifed. One strategy to overcome that p...
© 2016 by the authors; licensee MDPI, Basel, Switzerland. Hepatocellular carcinoma (HCC) is one of t...
In the present study, we investigated the in vitro antitumor functions of a synthetic chalcone deriv...
We previously reported that prenylated chalcone 2 (PC2), the O-prenyl derivative (2) of 2′-hydroxy-3...
We previously reported that prenylated chalcone 2 (PC2), the O-prenyl derivative (2) of 2'-hydroxy-3...
We previously reported that prenylated chalcone 2 (PC2), the O-prenyl derivative (2) of 2′-hydroxy-3...
Aim Chalcones are naturally occurring compounds with recognized anticancer activity. It was recently...
The p53 protein is one of the most important tumor suppressors that are frequently inactivated in ca...
Naturally-occurring chalcones and synthetic chalcone analogues have been demonstrated to have many b...
[[abstract]]Combination of selecting agents that act on different cellular mechanisms is a common st...
[[abstract]]Paclitaxel is a potential cancer chemotherapeutic agent for ovary, breast, and head and ...
The taxanes are effective microtubule-stabilizing chemotherapy drugs that inhibit mitosis, induce ap...
Chalcones are valuable structures for drug discovery due to their broad bioactivity spectrum. In thi...
International audienceChalcones are naturally occurring compounds with diverse pharmacological activ...
Naturally-occurring chalcones and synthetic chalcone analogues have been demonstrated to have many b...
Resistance to some cancer chemotherapeutic drugs has been identifed. One strategy to overcome that p...
© 2016 by the authors; licensee MDPI, Basel, Switzerland. Hepatocellular carcinoma (HCC) is one of t...
In the present study, we investigated the in vitro antitumor functions of a synthetic chalcone deriv...