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Circulating tumor cells drive metastasis and chemoresistance

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In the Woodfield lab at Texas Children's Hospital/Baylor College of Medicine, we are dedicated to deciphering how tumor cells invade into blood vessels, survive in systemic circulation, extravasate at distant organ sites, seed new malignant growths, and resist standard therapies.

Metastasis is the leading cause of cancer-related death. Patients with metastatic disease have much worse outcomes compared to those with localized disease.

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Metastasis marked by Beta-catenin (brown) in the mouse lung of one of our PDX models of hepatoblastoma.

Many of the same pathways that drive metastasis also play important roles in chemoresistance. Thus, cells that resist standard chemotherapies are predisposed to be able to metastasize. Conversely, cancer cells that metastasize are more likely to be chemoresistant.

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Patient-derived cell line developed in our lab from a chemoresistant hepatoblastoma tumor.

In the Woodfield lab, our goal is to understand how cancer cells metastasize so that we can design better therapeutic strategies that specifically target disseminated disease. All of our work focuses on pediatric liver cancer as a disease model for solid tumor metastasis.

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Tumor grown in the liver of a mouse from the human HepT1 cell line.

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