Culture-Based High Throughput Screen Detects Potent Anti-Ovarian Cancer Drugs

To incorporate the tumor microenvironment into the drug screening process, investigators at the University of Chicago (IL, USA) coated the wells of 384- and 1,536-well microtiter plates with a multilayered cellular mixture containing primary human fibroblasts, mesothelial cells, and extracellular matrix. Cultures of fluorescently labeled ovarian cancer cells from three different lines (HeyA8, SKOV3ip1, and Tyk-nu) were added to the wells and then exposed to a library of small-molecule compounds. The numbers of adhering and invasive ovarian cancer cells were counted, and the inhibitory potential of each compound evaluated.

Results published in the February 5, 2015, online edition of the journal Nature Communications revealed that in the initial screen of 2,420 compounds there were 17 compounds that inhibited cell adhesion and invasion by at least 75%. Six of these compounds were active in a dose-response relationship in all three ovarian cancer cell lines, and four compounds significantly inhibited key ovarian cancer cell functions in the early steps of metastasis at low doses. One of the compounds, beta-escin, which is isolated from the seeds of the Chinese horse chestnut, was found to inhibit tumor growth and metastasis by 97%.

"Visualizing how cancer cells interact with a tumor microenvironment that accurately reflects the complex biology of ovarian cancer should help us understand the mechanisms underlying metastatic progression as well as identify new therapeutics that can inhibit this process," said senior author Dr. Ernst Lengyel, professor of obstetrics and gynecology at the University of Chicago. "We think this novel screening system has the potential to uncover new, more effective medications that could be targeted more specifically at a patient's cancer."

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