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dc.contributor.authorChen, KTen_US
dc.contributor.authorLin, JDen_US
dc.contributor.authorChao, TCen_US
dc.contributor.authorHsueh, Cen_US
dc.contributor.authorChang, CAen_US
dc.contributor.authorWeng, HFen_US
dc.contributor.authorChan, ECen_US
dc.date.accessioned2014-12-08T15:44:24Z-
dc.date.available2014-12-08T15:44:24Z-
dc.date.issued2001-01-01en_US
dc.identifier.issn1050-7256en_US
dc.identifier.urihttp://hdl.handle.net/11536/29994-
dc.description.abstractPatients with follicular thyroid carcinoma have a higher incidence of metastasis than papillary thyroid carcinoma when thyroid cancer is diagnosed. The cDNA expression array technology is utilized herein to profile differentially expressed genes from metastatic human follicular thyroid carcinoma and reveal new tumor markers as well as target genes for therapeutic intervention. Tissue samples were obtained during surgical resection of the thyroid follicular carcinoma and metastatic tissue in the brain of the same patient. Two identical Atlas human cDNA expression arrays were hybridized with P-32-labeled cDNA probes derived from RNA of either primary thyroid cancer or metastatic tissue. Parallel analysis of the hybridized signals allowed us to identify the alteration of gene expression in the metastasis process. Eighteen genes significantly overexpressed and 40 genes significantly underexpressed were identified in the metastatic thyroid cancer. Genes that displayed an altered expression were associated with the processes of cell cycle regulation, apoptosis, DNA damage response, angiogenesis, cell adhesion and mobility, invasion, and immune response. An expression profile of genes that are associated with metastasis process of follicular thyroid cancer was also discussed. Further investigation is required to understand the precise relationship between the altered expression of these genes and the metastasis process of follicular thyroid cancer.en_US
dc.language.isoen_USen_US
dc.titleIdentifying differentially expressed genes associated with metastasis of follicular thyroid cancer by cDNA expression arrayen_US
dc.typeArticleen_US
dc.identifier.journalTHYROIDen_US
dc.citation.volume11en_US
dc.citation.issue1en_US
dc.citation.spage41en_US
dc.citation.epage46en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000166894300007-
dc.citation.woscount33-
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