Early detection of tumor response by FLT/microPET Imaging in a C26 murine colon carcinoma solid tumor animal model.

Fluorine-18 fluorodeoxyglucose ((18)F-FDG) positron emission tomography (PET) imaging demonstrated the change of glucose consumption of tumor cells, but problems with specificity and difficulties in early detection of tumor response to chemotherapy have led to the development of new PET tracers. Flu...

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Publicado en:Journal of Biomedicine & Biotechnology pp. 535902 - 535903
Autores principales: Lee, Wan-Chi, Chang, Chih-Hsien, Ho, Chung-Li, Chen, Liang-Cheng, Wu, Yu-Hsien, Chen, Jenn-Tzong, Wang, Ying-Ling, Lee, Te-Wei
Formato: research Journal Article
Publicado: Wiley-Blackwell 2011
Acceso en línea:Ver este registro en EBSCOhost
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      pub: Wiley-Blackwell
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        atl: Early detection of tumor response by FLT/microPET Imaging in a C26 murine colon carcinoma solid tumor animal model.
      aug:
        au:
          Lee, Wan-Chi
          Chang, Chih-Hsien
          Ho, Chung-Li
          Chen, Liang-Cheng
          Wu, Yu-Hsien
          Chen, Jenn-Tzong
          Wang, Ying-Ling
          Lee, Te-Wei
        affil: Isotope Application Division, Institute of Nuclear Energy Research, Taoyuan 32546, Taiwan.
      sug:
        subj:
          Colonic Neoplasms Drug Therapy
          Colonic Neoplasms Radiography
          Deoxyribonucleosides Diagnostic Use
          Tomography, Emission-Computed Methods
          Radiopharmaceuticals Diagnostic Use
          Animals
          Antibiotics, Antineoplastic Administration and Dosage
          Colonic Neoplasms Metabolism
          Deoxyribonucleosides Pharmacokinetics
          Doxorubicin Administration and Dosage
          Fludeoxyglucose F 18 Diagnostic Use
          Fludeoxyglucose F 18 Pharmacokinetics
          Male
          Mice
          Radiopharmaceuticals Pharmacokinetics
          Male
      ab: Fluorine-18 fluorodeoxyglucose ((18)F-FDG) positron emission tomography (PET) imaging demonstrated the change of glucose consumption of tumor cells, but problems with specificity and difficulties in early detection of tumor response to chemotherapy have led to the development of new PET tracers. Fluorine-18-fluorothymidine ((18)F-FLT) images cellular proliferation by entering the salvage pathway of DNA synthesis. In this study, we evaluate the early response of colon carcinoma to the chemotherapeutic drug, lipo-Dox, in C26 murine colorectal carcinoma-bearing mice by (18)F-FDG and (18)F-FLT. The male BALB/c mice were bilaterally inoculated with 1 x 10(5) and 1 x 10(6) C26 tumor cells per flank. Mice were intravenously treated with 10 mg/kg lipo-Dox at day 8 after (18)F-FDG and (18)F-FLT imaging. The biodistribution of (18)F-FDG and (18)F-FLT were followed by the microPET imaging at day 9. For the quantitative measurement of microPET imaging at day 9, (18)F-FLT was superior to (18)F-FDG for early detection of tumor response to Lipo-DOX at various tumor sizes (P < 0.05). The data of biodistribution showed similar results with those from the quantification of SUV (standard uptake value) by microPET imaging. The study indicates that (18)F-FLT/microPET is a useful imaging modality for early detection of chemotherapy in the colorectal mouse model.
      pubtype: Academic Journal
      doctype:
        research
        Journal Article
      ougenre: Article
    language: English
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