2010 Fiscal Year Final Research Report
Genes associated with brain-tropic human melanoma cells and their function
Project/Area Number |
21791092
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
Dermatology
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Research Institution | Jichi Medical University |
Principal Investigator |
SATO Atsuko Jichi Medical University, 医学部, 助教 (50382916)
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Project Period (FY) |
2009 – 2010
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Keywords | メラノーマ / 転移 |
Research Abstract |
Metastasis formation is responsible for most cancer deaths. Brain metastases, most often with melanomas as with lung and breast carcinomas, induce a high morbidity and mortality. Our analysis of many human cancer cell lines using bio-luminescent imaging (BLI) technology, has demonstrated cancer cell-type dependent metastasis to specific organs of NOD/SCID mice. Herein we established brain-tropic melanoma cell lines (SK-MEL-28-luc-br2 and Mewo-luc-br2) after 3 cycles of sequential intra-cardiac (i.e.) inoculation into mice, and determined the kinetics of brain accumulation of melanoma cells after i.e. injection. While both the brain-tropic and the low-metastatic melanoma (SK-MEL-2-luc) cells were present to similar degrees in the brain 0.5-5 hrs after injection, brain-tropic melanoma cells showed a significant increase in tumor-derived photons at the late phase (after 15-20 days). Further a comprehensive transcriptome analysis showed a significant increase (3-6 fold) of TGF-beta receptor II in brain-tropic melanoma and breast carcinoma (MDA-MB-231-luc-brl) cells. The BLI-mediated in vivo imaging should promote identification of potential molecular markers for cancer metastasis.
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