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Anti-tumor effects of shikonin derivatives on human medullary thyroid carcinoma cells.
Hasenoehrl, Carina; Schwach, Gert; Ghaffari-Tabrizi-Wizsy, Nassim; Fuchs, Robert; Kretschmer, Nadine; Bauer, Rudolf; Pfragner, Roswitha.
Afiliação
  • Hasenoehrl C; Institute of Pathophysiology and ImmunologyCenter of Molecular Medicine, Medical University of Graz, Graz, Austria.
  • Schwach G; Institute of Pathophysiology and ImmunologyCenter of Molecular Medicine, Medical University of Graz, Graz, Austria.
  • Ghaffari-Tabrizi-Wizsy N; Institute of Pathophysiology and ImmunologyCenter of Molecular Medicine, Medical University of Graz, Graz, Austria.
  • Fuchs R; SFL Chicken CAM LabInstitute of Pathophysiology and Immunology, Medical University of Graz, Graz, Austria.
  • Kretschmer N; Institute of Pathophysiology and ImmunologyCenter of Molecular Medicine, Medical University of Graz, Graz, Austria.
  • Bauer R; Department of PharmacognosyInstitute of Pharmaceutical Sciences, University of Graz, Graz, Austria.
  • Pfragner R; Department of PharmacognosyInstitute of Pharmaceutical Sciences, University of Graz, Graz, Austria.
Endocr Connect ; 6(2): 53-62, 2017 Feb.
Article em En | MEDLINE | ID: mdl-28069896
ABSTRACT
New treatment options are needed for medullary thyroid carcinoma (MTC), a highly metastasizing neuroendocrine tumor that is resistant to standard radiotherapy and chemotherapy. We show that the following shikonin derivatives inhibit cell proliferation and cell viability of the MTC cell line TT acetylshikonin, ß,ß-dimethylacrylshikonin, shikonin and a petroleum ether extract of the roots of Onosma paniculata containing several shikonin derivatives. The unsubstituted shikonin derivative was found to be the most effective compound with an IC50 of 1.1 µM. The cell viability of normal human skin fibroblasts, however, was not affected by the tested substances, indicating that shikonin derivatives might be selectively toxic for cancer cells. We further report that migration and invasion of TT cells were inhibited at non-toxic concentrations. Finally, shikonin was tested in vivo using the chick chorioallantoic membrane assay, where it significantly reduced tumor growth by inhibiting cell proliferation and inducing apoptosis. In summary, our results suggest that shikonin derivatives have the potential for the treatment of medullary thyroid carcinomas.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Endocr Connect Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Áustria

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Endocr Connect Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Áustria