Growth inhibitory potential of effective microorganism fermentation extract (EM-X) on cancer cells.

  • Chung Hin Chui
  • , Gregory Yin Ming Cheng
  • , Bin Ke
  • , Fung Yi Lau
  • , Raymond Siu Ming Wong
  • , Stanton Hon Lung Kok
  • , Sarwat Fatima
  • , Filly Cheung
  • , Chor Hing Cheng
  • , Albert Sun Chi Chan
  • , Cheuk On Tang

Research output: Journal article publicationJournal articleAcademic researchpeer-review

24 Citations (Scopus)

Abstract

The effective microorganism (EM-X) fermentation extract is derived from rice bran and seaweed extract. It has been shown to possess anti-oxidation activity both in vitro and in vivo. To our knowledge, the possible in vitro anti-cancer potential of EM-X has not been demonstrated. Here we showed that the double concentrate of EM-X (EM-X2) at concentrations of 20-30% by volume, had growth inhibitory activity on MDA-MB231 breast cancer cell line and K-562 chronic myelogenous leukaemia cell lines by [3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2-H-tetrazolium, inner salt] (MTS) assay. No characteristic features of apoptosis could be observed morphologically. Colony formation assay illustrated that both MDA-MB231 breast cancer and K-562 CML cells lost part of their regeneration potential after treatment with EM-X2 at 30% concentration by volume for 24 h. At these concentrations, only slight growth inhibitory effect was observed in 293 human kidney fibroblast cells and in three non-malignant bone marrows. Intracellular nitro blue tetrazolium (NBT) reduction assay showed that both MDA-MB231 breast cancer and K-562 CML cells had about 30% reduction of intracellular NBT after incubation with 30% of EM-X2. Increased activity of superoxide dismutase (SOD) could be detected from both MDA-MB231 and K-562 cell lines after incubating with 30% of EM-X2. Taken together, our data suggested that EM-X could inhibit growth and reduce the regeneration potential of cancer cells, possibly through its antioxidation activity.
Original languageEnglish
Pages (from-to)925-929
Number of pages5
JournalInternational Journal of Molecular Medicine
Volume14
Issue number5
Publication statusPublished - 1 Nov 2004

ASJC Scopus subject areas

  • Genetics

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