Tuesday,
April 30th
McCormick
& Schmicks
11:30
am check-in, 12 noon lunch & talk
RSVP
here. $30. Students & researchers, no cost.
Van
Vo is a PhD candidate at UNLV. Her research involves developing cisplatin
analogues for the treatment of cancer
The
In Vitro Cytotoxic Effects of Cisplatin Analogues in Cancer and Normal Cells by
Van Vo, Ontida Tanthmanatham, Haesook Han, Pradip K. Bhowmik and Bryan L.
Spangelo, UNLV Department of Chemistry
About
50% of cancer chemotherapeutic regimens consist of platinum-based drugs.
Cisplatin (CDDP) was the first platinum(II) complex approved for clinical
treatment by the U.S. Food and Drug Administration (FDA) in 1978. Along with
cisplatin, two other platinum(II) complexes, carboplatin and oxaliplatin, are
now approved for use worldwide.
Although
commonly prescribed, clinical application of platinum drugs is limited due to
narrow spectra of activity, cellular resistance, and toxic side effects. As a
consequence of
these
drawbacks, the search for improved drugs continues with the goal of discovering
compounds with greater efficacy and reduced toxicity.
Cisplatin
is not routinely used for the treatment of breast cancer since many breast
cancers are resistant to cisplatin treatment; however, it has been reported
that some breast
cancers
are sensitive to cisplatin. In an effort to develop improved platinum drugs for
the treatment of breast cancers, new platinum-complexes have been synthesized.
In vitro studies in various human breast
cancer cells demonstrated that these compounds are much more potent than
cisplatin. One of the synthesized complexes was also tested in a normal human
breast cell line and was found to be more toxic to the normal cells compared to
cancer cells. However, when this compound was tested in vivo in a mouse model,
the animals survived after administration of the compound at a dose of 12.5
mg/kg/day for three days. Further studies are required to assess the potential
translation of these compounds into clinical use.
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