Phytochemical Profiling and In Vitro Mechanistic Evaluation of Dichloromethane Extract from Phyllanthus emblica Fruit for Cancer Chemoprevention
Sirinya Taya, Chonikarn Singai, Rawiwan Wongpoomchai and Orawan Khantamat* Author for corresponding; e-mail address: orawan.kh@cmu.ac.th
Volume: Vol.52 No.6 (November 2025)
Research Article
DOI: https://doi.org/10.12982/CMJS.2025.102
Received: 1 June 2025, Revised: 29 September 2025, Accepted: 12 November 2025, Published: 27 November 2025
Citation: Taya S., Singai C., Wongpoomchai R. and Khantamat O., Phytochemical profiling and in vitro mechanistic evaluation of dichloromethane extract from Phyllanthus emblica fruit for cancer chemoprevention. Chiang Mai Journal of Science, 2025; 52(6): e2025102. DOI 10.12982/CMJS.2025.102.
Graphical Abstract
Abstract
Phyllanthus emblica, a traditional Thai medicinal plant, was investigated for its chemopreventive potential through comprehensive phytochemical profiling and mechanistic evaluation of its dichloromethane extract (DCME) and silica gel column fractions (D1, D2, D3). Advanced LC-MS/MS analysis, coupled with HPLC, identified phenolic acids, flavonoids, and other bioactive compounds as major constituents, with D2 demonstrating selective enrichment in phenolic content and superior antioxidant capacity. DCME and D2 exhibited selective cytotoxicity against hepatocellular carcinoma HepG2 cells and colorectal cancer SW480 cells, while maintaining minimal toxicity to normal human fibroblasts MRC5 cells. Both extracts displayed significant antimutagenic activity against aflatoxin B1 and MeIQ-induced mutations in Salmonella typhimurium strains. Uniquely, fraction D1 induced NADPH:quinone oxidoreductase (NQO) activity, suggesting enhanced phase II detoxification pathway activation. DCME demonstrated superior overall bioactivity compared to individual fractions, likely attributable to synergistic interactions among its diverse phytochemical profile. These preliminary findings suggest the potential of P. emblica, particularly DCME and D2, as natural chemopreventive agents and provide mechanistic insights that warrant further in vivo validation and therapeutic exploration.