Positron emission tomography imaging of DMBA/TPA mouse skin multi-step tumorigenesis

Ishikawa, Tomo-o; Kumar, Indracanti Prem; Machado, Hidevaldo B.; Wong, Koon-Pong; Kusewitt, Donna; Huang, Sung-Cheng; Fischer, Susan M.; Herschman, Harvey R.

doi:10.1016/j.molonc.2010.01.005

« Previous Next »Molecular Oncology
Volume 4, Issue 2 , Pages 119-125, April 2010

Positron emission tomography imaging of DMBA/TPA mouse skin multi-step tumorigenesis

Tomo-o Ishikawa
- Department of Molecular and Medical Pharmacology, David Geffen School of Medicine, UCLA, Los Angeles, CA 90095, USA
Indracanti Prem Kumar
- Department of Molecular and Medical Pharmacology, David Geffen School of Medicine, UCLA, Los Angeles, CA 90095, USA
Hidevaldo B. Machado
- Department of Molecular and Medical Pharmacology, David Geffen School of Medicine, UCLA, Los Angeles, CA 90095, USA
Koon-Pong Wong
- Department of Molecular and Medical Pharmacology, David Geffen School of Medicine, UCLA, Los Angeles, CA 90095, USA
Donna Kusewitt
- The University of Texas MD Anderson Cancer Center, Smithville, TX 78957, USA
Sung-Cheng Huang
- Department of Molecular and Medical Pharmacology, David Geffen School of Medicine, UCLA, Los Angeles, CA 90095, USA
Susan M. Fischer
- The University of Texas MD Anderson Cancer Center, Smithville, TX 78957, USA
Harvey R. Herschman
- Department of Molecular and Medical Pharmacology, David Geffen School of Medicine, UCLA, Los Angeles, CA 90095, USA
- Department of Biological Chemistry, David Geffen School of Medicine, UCLA, Los Angeles, CA 90095, USA
- Corresponding author at: 341 Boyer Hall, UCLA, 611 Charles E. Young Drive East, Los Angeles, CA 90095, USA. Tel.: +1 310 825 8735; fax: +1 310 825 1447.

Received 15 January 2010; received in revised form 23 January 2010; accepted 24 January 2010. published online 11 February 2010.

Abstract

Many tumor cells have elevated rates of glucose uptake that can be measured quantitatively, noninvasively and repeatedly by positron emission tomography (PET) with 2-deoxy-2-[¹⁸F]-fluoro-D-glucose (¹⁸F-FDG). Clinical imaging with ¹⁸F-FDG PET has been used for detection and staging of primary and metastatic tumors. High-resolution microPET scanning and murine cancer models make it possible to analyze longitudinally glucose metabolism during the appearance, development and progression of individual experimental tumors. In this study, we used ¹⁸F-FDG microPET and micro computerized tomography (microCT) to investigate glucose uptake in the DMBA/TPA chemically-induced multistage mouse skin carcinogenesis model. ¹⁸F-FDG uptake is significantly higher in all papillomas than in surrounding skin. Elevated ¹⁸F-FDG uptake is observed when tumors can be identified morphologically, but not before. Although ¹⁸F-FDG uptake is high in all fully invasive, malignant skin squamous cell carcinomas, uptake in papillomas and microinvasive malignant squamous cell carcinomas is variable and does not exhibit any correlation with tumor stage.

Keywords: Glucose metabolism, PET, Skin cancer, Molecular imaging, Fluorodeoxyglucose