Combretastatin A-4 and doxorubicin combination treatment is effective in a preclinical model of human medullary thyroid carcinoma.

  • Authors:
    • B D Nelkin
    • D W Ball
  • View Affiliations

  • Published online on: January 1, 2001     https://doi.org/10.3892/or.8.1.157
  • Pages: 157-217
Metrics: Total Views: 0 (Spandidos Publications: | PMC Statistics: )
Total PDF Downloads: 0 (Spandidos Publications: | PMC Statistics: )


Abstract

Medullary thyroid carcinoma (MTC), both in patients and in preclinical models, is resistant to chemotherapy. In this study, we show that the anti-neovascular agent combretastatin A-4 phosphate prodrug (CA4P) in combination with doxorubicin was effective in curtailing tumor growth in a preclinical model of human MTC. This combination of combretastatin and doxorubicin extended the doubling time of established MTC tumors in nude mice to 29 days, compared to 12 days in untreated controls. This suggests that a combination of combretastatin and a cytotoxic chemotherapeutic agent may be an effective treatment for MTC.

Related Articles

Journal Cover

January-February 2001
Volume 8 Issue 1

Print ISSN: 1021-335X
Online ISSN:1791-2431

Sign up for eToc alerts

Recommend to Library

Copy and paste a formatted citation
x
Spandidos Publications style
Nelkin B and Ball D: Combretastatin A-4 and doxorubicin combination treatment is effective in a preclinical model of human medullary thyroid carcinoma.. Oncol Rep 8: 157-217, 2001.
APA
Nelkin, B., & Ball, D. (2001). Combretastatin A-4 and doxorubicin combination treatment is effective in a preclinical model of human medullary thyroid carcinoma.. Oncology Reports, 8, 157-217. https://doi.org/10.3892/or.8.1.157
MLA
Nelkin, B., Ball, D."Combretastatin A-4 and doxorubicin combination treatment is effective in a preclinical model of human medullary thyroid carcinoma.". Oncology Reports 8.1 (2001): 157-217.
Chicago
Nelkin, B., Ball, D."Combretastatin A-4 and doxorubicin combination treatment is effective in a preclinical model of human medullary thyroid carcinoma.". Oncology Reports 8, no. 1 (2001): 157-217. https://doi.org/10.3892/or.8.1.157