Literature DB >> 18376305

Real-time high-resolution compound imaging allows percutaneous initiation and surveillance in an orthotopic murine pancreatic cancer model.

Carsten Ziske1, Klaus Tiemann, Tanja Schmidt, Srinivas Nagaraj, Angela Märten, Volker Schmitz, Ricarda Clarenbach, Tilman Sauerbruch, Ingo G H Schmidt-Wolf.   

Abstract

OBJECTIVES: Orthotopic tumor models are regarded as being suitable for preclinical research on pancreatic cancer. The anatomic localization of the tumor in the retroperitoneum, however, provides little possibility for monitoring tumor growth.
METHODS: To assess time-related changes in orthotopic tumor volume, we applied transabdominal high-resolution compound imaging to the murine pancreas. A 15-MHz ultrasound probe was used to determine the feasibility of real-time transabdominal high-resolution ultrasonography to initiate tumor growth by inoculation of pancreatic tumor cells into the pancreas and monitor tumor growth, as well as use as a tool for assessing response to chemotherapy.
RESULTS: High-resolution ultrasound allows for precise tumor inoculation in the pancreas. Sonographic-evaluated tumor weight was found to be closely related to actual tumor weight (R = 0.97) measured during necropsy.
CONCLUSIONS: High-resolution real-time compound imaging substitutes killing of mice during longitudinal studies and can be used for minimizing animal consumption because each mouse can be followed in an experimental group rather than having to resort to euthanasia for tissue harvesting.

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Year:  2008        PMID: 18376305     DOI: 10.1097/MPA.0b013e3181586cd9

Source DB:  PubMed          Journal:  Pancreas        ISSN: 0885-3177            Impact factor:   3.327


  6 in total

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5.  Use of Transabdominal Ultrasound for the detection of intra-peritoneal tumor engraftment and growth in mouse xenografts of epithelial ovarian cancer.

Authors:  Laura M Chambers; Emily Esakov; Chad Braley; Mariam AlHilli; Chad Michener; Ofer Reizes
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6.  Over-expression of miR-106b promotes cell migration and metastasis in hepatocellular carcinoma by activating epithelial-mesenchymal transition process.

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  6 in total

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