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Cell Biol Educ 4(3): 221-234 2005
DOI: 10.1187/cbe.04-10-0053
© 2005 American Society for Cell Biology
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ARTICLES

Students Investigating the Antiproliferative Effects of Synthesized Drugs on Mouse Mammary Tumor Cells

Rasha Hammamieh*, Margery Anderson*, Katharine Carr{dagger},§, Christine N. Tran{ddagger},§, Debra L. Yourick*, and Marti Jett*

* Walter Reed Army Institute of Research, Division of Pathology, 503 Robert Grant Avenue, Silver Spring, MD 20910;{dagger} Emory University, 201 Dowman Road, Atlanta, GA 30322; {ddagger} Cornell University, Department of Biomolecular and Chemical Engineering, Ithaca, NY 14850

Address correspondence to: Rasha Hammamieh (rasha.hammamieh{at}na.amedd.army.mil).

The potential for personalized cancer management has long intrigued experienced researchers as well as the naïve student intern. Personalized cancer treatments based on a tumor's genetic profile are now feasible and can reveal both the cells' susceptibility and resistance to chemotherapeutic agents. In a weeklong laboratory investigation that mirrors current cancer research, undergraduate and advanced high school students determine the efficacy of common pharmacological agents through in vitro testing. Using mouse mammary tumor cell cultures treated with "unknown" drugs historically recommended for breast cancer treatment, students are introduced to common molecular biology techniques from in vitro cell culture to fluorescence microscopy. Student understanding is assessed through laboratory reports and the successful identification of the unknown drug. The sequence of doing the experiment, applying logic, and constructing a hypothesis gives the students time to discover the rationale behind the cellular drug resistance assay. The breast cancer experiment has been field tested during the past 5 yr with more than 200 precollege/undergraduate interns through the Gains in the Education of Mathematics and Science program hosted by the Walter Reed Army Institute of Research.

Key Words: undergraduate • secondary • mouse tumor cells • breast cancer • personalized cancer management • genomic profiling • cellular drug resistance assay







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