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Abstract
"The use of the type 2 diabetics drug
metformin has been correlated with enhanced progression-free survival in
ovarian cancer.
The literature has speculated that this enhancement
is due to the high concentration of metformin directly causing cancer
cell death. However, this explanation does not fit
with clinical data reporting that the women exposed to constant
micromolar
concentrations of metformin, as present in the
treatment of diabetes, respond better to chemotherapy. Herein, our aim
was
to examine whether micromolar concentrations of
metformin alone could bring about cancer cell death and whether
micromolar
metformin could increase the cytotoxic effect of
commonly used chemotherapies in A2780 and SKOV3 cell lines and primary
cultured
cancer cells isolated from the peritoneal fluid of
patients with advanced ovarian cancer. Our results in cell lines
demonstrate
that no significant loss of viability or change in
cell cycle was observed with micromolar metformin alone; however, we
observed
cytotoxicity with micromolar metformin in
combination with chemotherapy at concentrations where the chemotherapy
alone produced
no loss in viability. We demonstrate that previous
exposure and maintenance of metformin in conjunction with carboplatin
produces
a synergistic enhancement in cytotoxicity of A2780
and SKOV3 cells (55% and 43%, respectively). Furthermore, in 5 (44%) of
the 11 ovarian cancer primary cultures, micromolar
metformin improved the cytotoxic response to carboplatin but not
paclitaxel
or doxorubicin. In conclusion, we present data that
support the need for a clinical study to evaluate the adjuvant
maintenance
or prescription of currently approved doses of
metformin during the chemotherapeutic treatment of ovarian cancer."
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