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A TRANSGENIC MOUSE FOR RAPID AND SENSITIVE IN VIVO TUMOR
DETECTION AND EVALUATION (SF03-069)
The number of murine models for human cancer has grown
rapidly in recent years and there now exist mouse models for almost all
tumor types. Evaluating the effect of specific molecular alterations or
therapeutic interventions in these animal models requires the ability to
temporally and spatially assess the tumor burden. In many cases, however,
this entails sacrificing the animal thereby limiting ability to perform
follow up analysis, and necessitating the use of many more experimental
animals.
To address these problems, UCSF investigators have generated a general “tumor
reporter” transgenic mouse strain designed to selectively expresses
firefly luciferase in malignant tissue. The luciferase gene is engineered
behind a region of the E2F-1 promoter, that is tumor cell specific.
Detecting the resulting light emissions enables sensitive and quantitative
detection of both primary and secondary tumors. These mice are designed
to be crossed with tumor prone mice in order to allow an investigator
to follow changes in tumor volume, for example in screening and evaluating
tumor response to therapeutic interventions. This technology may accelerate
and streamline the use of oncogene-driven tumor models for drug discovery
and phenotyping novel target transgenics.
In preliminary experiments, our investigators have successfully crossed
EF2-luciferase mice to visualize tumors in a number of experimental
models including spontaneous mouse metastatic prostate cancer model
(TRAMP) and a chemical carcinogen derived skin tumor model.
ADVANTAGES:
- Allows quantitative temporal and spatial assessment/monitoring
of tumor progression.
- Allows examination of primary tumors in
an immune competent animal.
- Allow potential detection of metastatic
disease and its response to treatment.
- Can be used to evaluate/validate
anti-cancer agents in vivo.
- Cost effective: animals do not need
to be sacrificed.
References: Hann, B. and Balmain, A. Building ‘validated’ mouse
models of human cancer. Curr. Op. Cell
Biol. (2001) 13(6):778.
If you would like to receive further information about
this technology and potential licensing opportunities, please contact:
Sunita Rajdev, Ph.D.
Licensing Officer
Phone: (415) 353-4470
Fax: (415) 348-1579
Sunita.rajdev@ucsf.edu
Reference: OTM Case #SF03-069
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