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NOBEL PRIZE 2026

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NIHNATIONAL CANCER INSTITUTER01

The role of multi-cellular aggregates vs. individual tumor cells in metastasis of high-grade serous ovarian cancer

Active
Institution
University of Wisconsin-Madison, WI
Principal investigator
Pamela K Kreeger
Funding
$510K
Duration
2020–2026
Open portfolio

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Abstract

Patients with high-grade serous ovarian cancer (HGSOC) are frequently diagnosed with extensive metastatic disease, resulting in a poor prognosis. In HGSOC, metastasis occurs primarily by transcoelomic spread, where tumor cells detach from the primary tumor, float through the peritoneal fluid, and attach to the mesothelial layer to form new metastases. Tumor cells in patient ascites exist as single cells or in multi-cellular aggregates similar in size to experimental spheroids. We hypothesize that single cell and aggregate-based metastasis are distinct processes in HGSOC transcoelomic spread. To test this hypothesis, we will utilize a combination of engineering-based approaches (in vitro culture systems, multivariate modeling, computational fluid dynamics) and biological methods (molecular and cellular assays, analysis of patient samples, xenograft models). This proposal leverages a diverse, collaborative team that includes experts in engineering, biology, and the clinical presentation of HGSOC. Completion of the proposed studies will result in an improved understanding of mechanisms regulating transcoelomic spread and identification of potential targets for future work to control metastatic spread.

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R01NATIONAL CANCER INSTITUTETumor Progression and Metastasis Study Section[TPM]metastasisovarian cancertumor cellsserousspreadhgsocaggregateshigh-grade

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