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      Novel three dimensional cultures provide insights into thyroid cancer behavior

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          Abstract

          Thyroid cancer has the fastest growing incidence of any cancer in the United States, as measured by the number of new cases per year. Despite advances in tissue culture techniques, a robust model for thyroid cancer spheroid culture has yet to be developed. Using eight established thyroid cancer cell lines, we created an efficient and cost-effective 3D culture system that can enhance our understanding of in vivo treatment response. We found that all eight cell lines readily form spheroids in culture with unique morphology, size, and cytoskeletal organization. In addition, we developed a high throughput workflow that allows for drug screening of spheroids. Using this approach, we found that spheroids from K1 and TPC1 cells demonstrate significant differences in their sensitivities to dabrafenib treatment, that closely model expected patient drug response. In addition, K1 spheroids have increased sensitivity to dabrafenib when compared to monolayer K1 cultures. Utilizing traditional 2D cultures of these cell lines we evaluated the mechanisms of this drug response, showing dramatic and acute changes in their actin cytoskeleton as well as inhibition of migratory behavior in response to dabrafenib treatment. Our study is the first to describe the development of a robust spheroid system from established cultured thyroid cancer cell lines and adaptation to a high throughput format. We show that combining 3D culture with traditional 2D methods provides a complementary and powerful approach to uncover drug sensitivity and mechanisms of inhibition in thyroid cancer.

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          Author and article information

          Journal
          9436481
          21439
          Endocr Relat Cancer
          Endocr. Relat. Cancer
          Endocrine-related cancer
          1351-0088
          1479-6821
          25 April 2020
          February 2020
          01 February 2021
          : 27
          : 2
          : 111-121
          Affiliations
          [1. ]Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN
          [2. ]Department of Pharmacology, Vanderbilt University, Nashville, TN
          [3. ]Department of Cell and Developmental Biology, Vanderbilt University, Nashville, TN
          [4. ]Department of Biochemistry, Vanderbilt University, Nashville, TN
          [5. ]University School of Nashville, 2000 Edgehill Avenue, Nashville, TN 37212
          Author notes
          Correspondence: Vivian Weiss, M.D. Ph.D., Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, 1161 21 st Ave. S., MCN C-3321, Nashville, TN 37232, Phone: 615-875-3002, Vivian.l.weiss@ 123456vanderbilt.edu
          Article
          PMC7295136 PMC7295136 7295136 nihpa1586858
          10.1530/ERC-19-0374
          7295136
          31804972
          6eeb9afb-f793-4a2f-a97f-d633bd8d63cd
          History
          Categories
          Article

          invasion,thyroid carcinoma,β-catenin,Spheroid,actin
          invasion, thyroid carcinoma, β-catenin, Spheroid, actin

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