Hopea odorata extract inhibits hepatocellular carcinoma via induction of caspase-dependent apoptosis

• Main Authors: Nguyen ST, Huynh KL, Nguyen HL, Nguyen Thi Thanh M, Nguyen Trung N, Nguyen Xuan H, Ngoc KP, Truong Dinh K, Pham PV
• Format: Article
• Language: English
• Published: Dove Medical Press 2017-12-01
• Series: OncoTargets and Therapy
• Subjects: Apoptosis; caspase-3; HepG2; Hopea odorata; human fibroblast; methanol extract; selectivity index
• Online Access: https://www.dovepress.com/hopea-odorata-extract-inhibits-hepatocellular-carcinoma-via-induction--peer-reviewed-article-OTT

Sinh Truong Nguyen,1,2 Khanh Linh Huynh,1 Huyen Lam-Thi Nguyen,1,2 Mai Nguyen Thi Thanh,3 Nhan Nguyen Trung,3 Hai Nguyen Xuan,3 Kim Phan Ngoc,1 Kiet Truong Dinh,4 Phuc Van Pham1,2 1Stem Cell Institute, 2Laboratory of Cancer Research, 3Faculty of Chemistry, University of Science, Vietnam National University Ho Chi Minh City, 4Medical Genetic Institute, Ho Chi Minh City, Vietnam Introduction: Cancer is a disease with a global burden and is a major and increasing threat to public health. The demand for new modalities to treat and prevent cancer is high. Given the toxic side effects of standard treatments, such as chemotherapy, there is greater research interest in naturally derived compounds due to their selective toxicity to cancer cells. This study aimed to test the anticancer activity of a crude extract of Hopea odorata on hepatocellular carcinoma (HCC) HepG2 cell line. Methods: Methanol extracts of H. odorata were prepared from the bark of H. odorata plants (H. odorata extract). The in vitro cytotoxicity of H. odorata extracts on human HCC cell line HepG2 compared to normal human fibroblasts (HFs) was assessed by Alamar Blue assay. Caspase-3/7 was detected using a reagent that consists of DEVD peptide conjugated to a nucleic acid-binding dye. Apoptosis induction by the H. odorata plant extract on HepG2 was evaluated by Annexin V/7-AAD using flow cytometry. Disintegrated nuclei of plant-treated cells were observed under a fluorescent microscope using Hoechst and propidium iodide (PI) staining. In addition, using the Hoechst/PI staining technique, the ratio of dead to total cells was determined by distinguishing Hoechst and PI fluorescent signals.Results: We found that the IC50 value of H. odorata extract on HepG2 was 12.67±5 µg/mL and on HF was 44±3 µg/mL. The IC50 value of doxorubicin on HepG2 was 153.3±15 ng/mL and on HF was 6.3±0.6 ng/mL. The selectivity index (SI) of H. odorata extract for HepG2 cells was ~3.48, while the SI of doxorubicin for HepG2 cells was ~0.04. The ratio of dead to total cells increased in a dose-dependent manner for HepG2 cells when observed under a fluorescent microscope, while the ratio of dead to total cells barely changed for HF cells. The H. odorata extract inhibited HepG2 cells via the activation of caspase-3/7. At 250 µg/mL concentration of the H. odorata extract, 35% of HepG2 cells were induced into apoptosis, and the cells exhibited disintegrated nuclei under a fluorescent microscope.Conclusion: These findings demonstrate that the methanolic bark extracts of H. odorata plant induce apoptosis and selective cytotoxicity toward HepG2 but not HF. Therefore, purification of compounds from H. odorata bark extracts may be useful as anticancer agents, and thus, more studies are warranted to investigate the anticancer properties of H. odorata. Keywords: apoptosis, caspase-3, HepG2, Hopea odorata, human fibroblast, methanol extract, selectivity index