The Inhibition Effect of 2-Methoxy-1,4- naphthoquinone on Human Hepatoma Cell Lines: A in vitro and in vivo Studies
Indian Journal of Pharmaceutical Education and Research
Huaguo Liang1School of Life Sciences and Biopharmaceutics, Guangdong Pharmaceutical University, Guangzhou, PR, CHINA., 2Guangzhou Key Laboratory of Construction and Application of New Drug Screening Model Systems, Guangdong Pharmaceutical University, Guangzhou, PR, CHINA.
Ying Wen1School of Life Sciences and Biopharmaceutics, Guangdong Pharmaceutical University, Guangzhou, PR, CHINA., 2Guangzhou Key Laboratory of Construction and Application of New Drug Screening Model Systems, Guangdong Pharmaceutical University, Guangzhou, PR, CHINA.
Wei Fang1School of Life Sciences and Biopharmaceutics, Guangdong Pharmaceutical University, Guangzhou, PR, CHINA.
Xiaoyan Cai1School of Life Sciences and Biopharmaceutics, Guangdong Pharmaceutical University, Guangzhou, PR, CHINA.
Xiangsheng Wang1School of Life Sciences and Biopharmaceutics, Guangdong Pharmaceutical University, Guangzhou, PR, CHINA.
Li Zou4School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, PR, CHINA.
Peng Wei1School of Life Sciences and Biopharmaceutics, Guangdong Pharmaceutical University, Guangzhou, PR, CHINA.
Baoyun Yang4School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, PR, CHINA.
Jiazheng Lu4School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, PR, CHINA.
Yongxia Yang3School of Medical Information Engineering, Guangdong Pharmaceutical University, Guangzhou, PR, CHINA.
Yongli Zhang1School of Life Sciences and Biopharmaceutics, Guangdong Pharmaceutical University, Guangzhou, PR, CHINA., 2Guangzhou Key Laboratory of Construction and Application of New Drug Screening Model Systems, Guangdong Pharmaceutical University, Guangzhou, PR, CHINA.
Background and Aim: To study the antitumor activity of 2-Methoxy-1,4-naphthoquinone (MNQ) against hepatocellular carcinoma (HCC) cells, in an attempt to fill the knowledge gap of anti-liver cancer with MNQ. Materials and Methods: Cell viability in the presence of MNQ was assessed by MTT and effect of MNQ on HepG2 cell cycle by flow cytometry. To analyze apoptosis and its molecular mechanisms, we used a combination of Hoechst 33342 staining, annexin V binding, Rhodamine 123 staining, Real-time quantitative PCR (qPCR), western blotting and confocal microscopy. On the other hand, in vivo tumor growth was measured by a xenograft tumor nude mice model. Finally, the hematoxylin and eosin staining were used to observe the pathological changes of tumor tissue. Results: The results indicate that MNQ induced apoptosis in HCC cell lines, as demonstrated by a significant increasing of mitochondrial membrane potential and G0/G1 cell cycle arrest in HepG2 cells. Furthermore, MNQ significantly up-regulated BAD and down-regulated the expression of anti-apoptotic factors NF-κB and Bcl-2 at protein and transcription levels. Finally, in vivo studies revealed that MNQ significantly inhibited tumor growth. Conclusion: MNQ suppress the proliferation and induces apoptosis of HCC cells through mitochondrial and Rel/NF-κB signal pathways.
