![Honors Theses and Capstones](../../assets/md5images/fe07a130f47f5b7a3139a0207be3f0bf.png)
Honors Theses and Capstones
Date of Award
Spring 2020
Project Type
Senior Honors Thesis
College or School
COLSA
Department
Department of Molecular, Cellular, and Biomedical Sciences
Program or Major
Biomedical Sciences
Degree Name
Bachelor of Science
First Advisor
Sarah Walker
Abstract
Ovarian cancer remains a deadly disease for countless women. Recent evidence demonstrates that ovarian cancer cell clusters, spheroids, are important in promoting ovarian recurrence and metastasis. Often these spheroids are resistant to therapy. Therefore, we were interested in identifying drugs that could target ovarian cancer spheroids. Analysis of gene expression identified the STAT3 signaling pathway as a pathway enriched in 3D growing ovarian cancer cells. STAT3 is a transcription factor that is activated by tyrosine phosphorylation in about 70% of high grade serous ovarian cancers. Using shRNA targeting STAT3 and the upstream signaling molecule, GP130, we found that reduction of both STAT3 and its upstream signaling molecule GP130 reduced the growth of spheroids. This suggested that targeting STAT3 or an upstream signaling molecule might be a viable treatment option. Atovaquone, used normally for the treatment of malaria or the prevention of pneumocystic pneumonia, inhibits STAT3 activation by inhibiting the expression of GP130 on the cell surface. Therefore, showing that atovaquone has potential in decreasing viability in ovarian cancer cells.
Recommended Citation
Neil, Kayli E., "Atovaquone Targets STAT3 in Ovarian Cancer Spheroids" (2020). Honors Theses and Capstones. 503.
https://scholars.unh.edu/honors/503