1 / 1

Name(s): Sajith Wickramasekara and Andrew Guo

Name(s): Sajith Wickramasekara and Andrew Guo High School(s): North Carolina School of Science and Mathematics Mentor: Dr. Craig B. Bennett Project Title: A Functional Genomic Framework for Chemotherapeutic Drug Improvement and Identification.

flower
Télécharger la présentation

Name(s): Sajith Wickramasekara and Andrew Guo

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Name(s): Sajith Wickramasekara and Andrew Guo High School(s): North Carolina School of Science and Mathematics Mentor: Dr. Craig B. Bennett Project Title: A Functional Genomic Framework for Chemotherapeutic Drug Improvement and Identification Chemotherapeutic drugs function by inducing cytotoxicity in rapidly dividing cells through mitotic impairment or forced apoptosis. It is common for non-cancerous cells to be affected by these drugs, resulting in detrimental side effects. To mediate these undesired responses, we proposed a genomic framework using the eukaryotic yeast Saccharomyces cerevisiae deletion collection to identify genes that confer resistance to DNA damaging agents including chemotherapeutic drugs. Based on the genomic conservation of yeast with humans, we determined human orthologs to our yeast targets and verified their roles in mediating cellular response to DNA damage. Our initial genome-wide screen in diploid yeast identified 376 genes that conferred resistance to the widely used G1/S phase chemotherapeutic drug, doxorubicin. A similar haploid yeast screen identified five-fold fewer targets, which, due to a lack of recombination ability in G1 haploids, suggests the presence of a G1/S specific DNA repair network in diploid yeast. To further test our framework we screened the G1 toxin zymocin and identified significant genetic overlap with the genes that mediate doxorubicin resistance, indicating zymocin’s potential as a chemotherapeutic agent. Successful development of our framework has direct application in sensitizing tumors, identifying novel treatments, and building a foundation for personalized medicine.

More Related