Identification of Protein Kinase Inhibitory Activities Fromstreptomyces Strain H7372 for Potential Use As Anti-Canceragent
Aberrations in the phospbatidylinositol3-kinase (PI3K)IAkt pathway have been found in a wide spectrum of human cancers. Activation of Akt and inactivation of the downstream substrates such as GSK-3P, BAD and Forkhead family (FKHR) proteins are relevant to promote cell survival, proliferation and...
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| Main Author: | |
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| Format: | Thesis |
| Language: | English |
| Published: |
2007
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| Subjects: | |
| Online Access: | http://psasir.upm.edu.my/id/eprint/6438/1/FPSK%28M%29_2007_18.pdf |
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| Summary: | Aberrations in the phospbatidylinositol3-kinase (PI3K)IAkt pathway have been found in
a wide spectrum of human cancers. Activation of Akt and inactivation of the
downstream substrates such as GSK-3P, BAD and Forkhead family (FKHR) proteins are
relevant to promote cell survival, proliferation and growth. Another related pathway
linked with PI3K/Akt is the Ras/Raf/MEK/ERK, which is known to promote cancer as a
result of ras-transformation. The discovery of new drugs targeted at specific molecules
of these pathways is a 'hot' field in cancer research. Blocking the constitutively active
PI3WAkt pathway provides a new strategy for cancer therapy. Thus, inhibitors of this
signaling pathway would be potential anti-cancer agents. The Streptomyces strain H7372
isolated h m mangrove soils in Sabah was found to inhibit the Ras/Raf-1 protein
interaction in the yeast two-hybrid screening system. The present study was undertaken
to determine the cytotoxic effect of H7372 hctionated extract on a breast cancer cell
line, MCF-7 and a non-tumorigenic epithelial cell line, MCF-1OA and quantitatively
measure kinase inhibition, apoptosis induction and cell cycle disruption. The crude
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extracts of H7372 were fractionated into eight Eractions using reverse phase HPLC.
Fraction 5 was found to be the most cytotoxic in an M'IT assay. The crude extract and
fraction 5 of H7372 were found to exert growth inhibition of MCF-7 at ICS0 of 15&nl
and 1.4 pglml, respectively. Western blot analyses showed that activated PI3K and Akt
(Thr308) but not Akt (Ser473) by stimulation of IGF-I were inhibited by the crude
extract and fraction 5 after 72 hours. Interestingly, phosphorylation of Raf-1 (Ser259)
and ERKl were also inhibited by fraction 5, indicated that there is a cross-talk between
PI3WAkl and MAPK pathways. By using the flow cytometry technique, we found that
fraction 5 inhibited the proliferation of MCF-7 cell line by causing them to arrest in the
GI phase of the cell cycle. The induction of growth arrest by fraction 5 was associated
with accumulation of cells in GI and decreasing cells in S and G2/M phases. The results
were supported by inihibition of cyclin Dl in MCF-7 cells. The apoptosis study showed
that fraction 5 but not crude extract was increased the percentage of cells in early
apoptotic stage at all concentrations. Furthermore, treatment of MCF-7 cells with
fraction 5 resulted in reduction in phosphorylation of GSK-3$ (Ser9), phospho-BAD
(Serll2) and phospho-FKHR (Ser256). These results could contribute the apoptosis in
MCF-7 cell line. Thus, we discovered that k t i o n 5 of H7372, a naturally occurring
microbe, contains an inhibitor of cell proliferation, cell cycle progression and is able to
induce apoptosis via the PI3WAkl and MAPK pathways. |
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