Our objective was to determine whether changes in PME and PCr/Pi can be used to predict lack of tumor response to chemotherapy in a murine model of human osteosarcoma. Cisplatin sensitive and resistant human osteosarcoma cell lines were implanted into a total of 22 nude mice. 3\*P MR spectroscopy wa
P-31 changes as a measure of therapy response in resistant and sensitive osteosarcomas implanted into nude mice
โ Scribed by J.R. Ballinger; H. Kang; C.A. Sweeney; J.D. Scott; B.P. Croker; K.N. Scott
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 734 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0730-725X
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โฆ Synopsis
Objective: To determine if changes in PCr/Pi and PME can be used to predict lack of tumor response to chemotherapy in a murine model of a chemotherapy-resistant human osteosarcoma. Material and Methods: Cisplatinresistant sublhtes were grown from high-grade cisplatin-sensitive human osteosarcoma. Surface coil localized 31P NMR spectroscopy of implanted cisplatin-resistant and sensitive osteosarcoma tumors in nude mice was performed. Results: A cisplatin-resistant subline of a sensitive human osteosarcoma was developed that was five times more resistant to cisplatin than the parent cell line. Our NMR data shows a statistically significant difference in the change in the PCr/Pi ratio after treatment between sensitive and resistant osteosarcomas at the 01 = 0.05 level. Changes in PME were seen in the sensitive tumors but were not statistically significant. Conclusions: Changes in PCr/Pi predict lack of tumor treatment response in human osteosarcoma implanted into nude mice with a specificity of 70% and a sensitivity of 54%. Monitoring of PCr/Pi in human osteosarcoma patients may allow detection of response to chemotherapy before conventional imaging techniques.
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