The Effects of 2′,4′-Dihydroxy-6′-methoxy-3′,5′- dimethylchalcone from <em>Cleistocalyx operculatus</em> Buds on Human Pancreatic Cancer Cell Lines
Huynh Nhu Tuan,
Bui Hoang Minh,
Phuong Thao Tran,
Jeong Hyung Lee,
Ha Van Oanh,
Quynh Mai Thi Ngo,
Yen Nhi Nguyen,
Pham Thi Kim Lien,
Manh Hung Tran
Affiliations
Huynh Nhu Tuan
Hanoi University of Pharmacy, 13 Le Thanh Tong Street, Hoan Kiem District, Hanoi 100100, Vietnam
Bui Hoang Minh
Faculty of Pharmacy, Nguyen Tat Thanh University, 300C Nguyen Tat Thanh Street, District 4, Hochiminh City 72820, Vietnam
Phuong Thao Tran
Department of Biochemistry, College of Natural Sciences, Kangwon National University, Chuncheon, Gangwon-Do 24414, Korea
Jeong Hyung Lee
Department of Biochemistry, College of Natural Sciences, Kangwon National University, Chuncheon, Gangwon-Do 24414, Korea
Ha Van Oanh
Hanoi University of Pharmacy, 13 Le Thanh Tong Street, Hoan Kiem District, Hanoi 100100, Vietnam
Quynh Mai Thi Ngo
College of Pharmacy, Hai Phong University of Medicine and Pharmacy, 72A Nguyen Binh Khiem, Hai Phong 180000, Vietnam
Yen Nhi Nguyen
Faculty of Biology and Biotechnology, University of Science, Vietnam National University Hochiminh City, 227 Nguyen Van Cu, District 5, Hochiminh City 748000, Vietnam
Pham Thi Kim Lien
Biomedical Sciences Department, Institute for Research & Executive Education (VNUK), The University of Danang, 158A Le Loi, Hai Chau District, Danang City 551000, Vietnam
Manh Hung Tran
Biomedical Sciences Department, Institute for Research & Executive Education (VNUK), The University of Danang, 158A Le Loi, Hai Chau District, Danang City 551000, Vietnam
2′,4′-Dihydroxy-6’-methoxy-3′,5′-dimethylchalcone (DMC), a principal natural chalcone of Cleistocalyx operculatus buds, suppresses the growth of many types of cancer cells. However, the effects of this compound on pancreatic cancer cells have not been evaluated. In our experiments, we explored the effects of this chalcone on two human pancreatic cancer cell lines. A cell proliferation assay revealed that DMC exhibited concentration-dependent cytotoxicity against PANC-1 and MIA PACA2 cells, with IC50 values of 10.5 ± 0.8 and 12.2 ± 0.9 µM, respectively. Treatment of DMC led to the apoptosis of PANC-1 by caspase-3 activation as revealed by annexin-V/propidium iodide double-staining. Western blotting indicated that DMC induced proteolytic activation of caspase-3 and -9, degradation of caspase-3 substrate proteins (including poly[ADP-ribose] polymerase [PARP]), augmented bak protein level, while attenuating the expression of bcl-2 in PANC-1 cells. Taken together, our results provide experimental evidence to support that DMC may serve as a useful chemotherapeutic agent for control of human pancreatic cancer cells.