Apoptotic potential of the concentrated effective microorganism fermentation extract on human cancer cells
The effective microorganism fermentation extract (EM-X, the first generation) was claimed to possess strong anti-oxidation property. On the other hand, we have shown that the second generation of the effective microorganism fermentation extract (EM-X2) possessed growth inhibition on human cancer cel...
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Veröffentlicht in: | International journal of molecular medicine 2006-02, Vol.17 (2), p.279-284 |
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Sprache: | eng |
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Zusammenfassung: | The effective microorganism fermentation extract (EM-X, the first generation)
was claimed to possess strong anti-oxidation property. On the other hand, we have
shown that the second generation of the effective microorganism fermentation extract
(EM-X2) possessed growth inhibition on human cancer cells involving MDA-MB231
breast cancer and K-562 chronic myelogenous leukaemia cells. Elevation of super
oxide dismutase activity from EM-X2 treated cancer cell extract was observed.
However, the possible anti-cancer activity of the first generation of the EM-X
was not reported. Here we demonstrate that the concentrated form of the EM-X from
its original fluid also possess antiproliferation ability together with induction
of apoptosis on the human cancer cell lines including Hep3B hepatocellular carcinoma
(HCC) and KG1a acute myelogenous leukaemia (AML). Similar effect could also be
demonstrated on primary cultured bone marrow samples isolated from patients with
AML. Morphological inspection revealed that common apoptotic feature was found
on these concentrated EM-X treated cancer cells. Both the anchorage-dependent
clonogenicity assay on Hep3B HCC and methyl-cellulose colony formation assay on
KG1a cells and bone marrow cells from AML patients further revealed the ability
of the concentrated EM-X on reducing their colony formation ability. Incubating
KG1a with concentrated EM-X readily induced apoptosis as demonstrated by flow
cytometric analysis. Interestingly, few growth inhibition effect of the concentrated
EM-X was observed on both the SV40 transformed THLE-2 liver epithelial cells and
primary cultured non-malignant haematological disordered bone marrow. Collectively,
this concentrated EM-X is effective in inducing cell death and reducing the regeneration
potential of both Hep3B HCC and KG1a AML cells in vitro. |
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ISSN: | 1107-3756 1791-244X |
DOI: | 10.3892/ijmm.17.2.279 |