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student research day - Case Western Reserve University School of ...

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Nicholas O. Schroeder<br />

3,4-Methylenedioxy-ß-nitrostyrene (MNS) and the reduction <strong>of</strong> colony<br />

formation in osteosarcoma cells and osteoblasts.<br />

Nicholas O. Schroeder, Ashley N. Rettew and Edward M. Greenfield<br />

Orthopaedics Department<br />

<strong>Case</strong> Medical Center<br />

MNS, a known inhibitor <strong>of</strong> platelet aggregation, has been shown previously to be an inhibitor <strong>of</strong> tyrosine kinases src and<br />

syk and is being studied as a potential chemotherapeutic agent for osteosarcoma. Our lab has previously shown that MNS<br />

inhibits motility and colony formation in vitro in two families <strong>of</strong> genetically-related human osteosarcoma cell lines: nontumorigenic/non-metastatic<br />

parental cell lines (TE85 and SAOS-2), a tumorigenic but non-metastatic cell line (MNNG),<br />

and highly tumorigenic/metastatic cell lines (143B and LM7). For this study, we examined the ability <strong>of</strong> MNS to inhibit<br />

colony formation and disrupt preformed colonies grown on collagen gels to mimic the microenvironment <strong>of</strong> the lung, the<br />

most common site for lethal micrometastases in osteosarcoma patients. MNS was shown to inhibit colony formation and<br />

quickly induce apoptosis in all five cell lines. Biochemical assays were also performed by an outside party to study the<br />

ability <strong>of</strong> MNS to inhibit a number <strong>of</strong> tyrosine kinases believed to be involved in osteosarcoma, including src and syk.<br />

Interestingly, MNS did not inhibit any tyrosine kinases, suggesting that it acts via a different mechanism<br />

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