Nucl Med Mol Imaging.  2010 Sep;44(3):165-169.

Early Metabolic Flare in Squamous Cell Carcinoma after Chemotherapy is a Marker of Treatment Sensitivity In Vitro

Affiliations
  • 1Department of Oncology, Lund University and Lund University Hospital, 221 85 Lund, Sweden. maria.bjurberg@med.lu.se
  • 2Vaccine Research Institute of San Diego, San Diego, CA, USA.
  • 3Clinical Sciences, Department of Oncology, Lund University, Lund, Sweden.
  • 4Department of Otorhinolaryngology and Head and Neck Surgery, Lund University Hospital, Lund, Sweden.
  • 5Department of Radiation Sciences, Umea University, Umea, Sweden.

Abstract

PURPOSE
Early metabolic response with a decrease in glucose demand after cytotoxic treatment has been reported to precede tumor volume shrinkage. However, preclinical studies report of a very early rise in metabolism, a flare, following treatment. To elucidate these observations, we performed an experimental study on early metabolic response with sequential analysis of metabolic changes.
METHODS
Three squamous cell carcinoma cell lines and one nontumorigenic cell line were exposed to cisplatin. The uptake of the fluorescent glucose analogue 2-NBDG was examined at days 1-6 using fluorescence microscopy. The relation between 2-NBDG-uptake and cell survival was evaluated.
RESULTS
The tumor cells exhibited a high uptake of 2-NBDG, whereas the uptake in the nonmalignant cells was low. The more cisplatin sensitive cell lines exhibited a more pronounced metabolic flare than the less sensitive cell line.
CONCLUSION
A metabolic flare was a very early sign of treatment response and potentially it could be used as an early marker of treatment sensitivity.

Keyword

FDG-PET; NBDG; Flare; Fluorescence; Chemotherapy; Squamous cell carcinoma

MeSH Terms

4-Chloro-7-nitrobenzofurazan
Carcinoma, Squamous Cell
Cell Line
Cell Survival
Cisplatin
Deoxyglucose
Fluorescence
Glucosamine
Glucose
Microscopy, Fluorescence
Tumor Burden
4-Chloro-7-nitrobenzofurazan
Cisplatin
Deoxyglucose
Glucosamine
Glucose
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