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논문 기본 정보

자료유형
학술저널
저자정보
Xia, Yi-Qun (Chemical Biology Research Center, College of Pharmaceutical Sciences, Wenzhou Medical University) Wei, Xiao-Yan (Chemical Biology Research Center, College of Pharmaceutical Sciences, Wenzhou Medical University) Li, Wu-Lan (Chemical Biology Research Center, College of Pharmaceutical Sciences, Wenzhou Medical University) Kanchana, Karvannan (Chemical Biology Research Center, College of Pharmaceutical Sciences, Wenzhou Medical University) Xu, Chao-Chao (Chemical Biology Research Center, College of Pharmaceutical Sciences, Wenzhou Medical University) Chen, Da-Hui (Chemical Biology Research Center, College of Pharmaceutical Sciences, Wenzhou Medical University) Chou, Pei-Hong (Chemical Biology Research Center, College of Pharmaceutical Sciences, Wenzhou Medical University) Jin, Rong (Department of Digestive Diseases, The First Affiliated Hospital of Wenzhou Medical University) Wu, Jian-Zhang (Chemical Biology Research Center, College of Pharmaceutical Sciences, Wenzhou Medical University) Liang, Guang (Chemical Biology Research Center, College of Pharmaceutical Sciences, Wenzhou Medical University)
저널정보
아시아태평양암예방학회 Asian Pacific journal of cancer prevention : APJCP Asian Pacific journal of cancer prevention : APJCP 제15권 제16호
발행연도
2014.1
수록면
6,893 - 6,898 (6page)

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Curcumin and its analogues have been reported to exert anti-cancer activity against a variety of tumors. Here, we reported A501, a new curcumin analogue. The effect of A501 on cell viability was detected by MTT assay, the result showed that A501 had a better inhibiting effect on the four non-small cell lung cancer (NSCLC) cells than that of curcumin. Moreover, Colony forming experiment showed A501 significant restrained cell proliferation. Flow cytometry displayed A501 can cause G2/M arrest and induce apoptosis. Western blotting showed that A501 decreased the expression of cyclinB1, cdc-2, bcl-2, while increased the expression of p53, cleaved caspase-3 and bax. In conclusion, curcumin analogues A501 played antitumor activity by inhibiting cell proliferation and inducing apoptosis of NSCLC cells. And it was likely to be a promising starting point for the development of curcumin-based anticancer drugs.

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