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http://purl.uniprot.org/citations/9393974http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/9393974http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/9393974http://www.w3.org/2000/01/rdf-schema#comment"Using differential display, we identified an mRNA that is markedly down-regulated in cell line 6A/SB1, derived from a fibrosarcoma formed in an athymic mouse following injection of carcinogen-transformed MSU-1.1 cells. The nontumorigenic parental cell strain, MSU-1.1, expresses high levels of this mRNA. Sequencing of the corresponding cDNA fragment revealed that it corresponded to an expressed sequence tag, which ultimately led to its identification as the fibulin-1D gene. Fibulin-1 is a cysteine-rich, calcium-binding extracellular matrix and plasma protein, which has four isoforms, A-D, derived from alternative splicing. Northern and Western blotting analysis of 16 cell lines established from tumors formed in athymic mice by MSU-1.1-derived cell strains independently transformed in culture showed that 44% exhibited low level or lack of expression of fibulin-1D mRNA and protein. In a similar analysis of 15 malignant cell lines derived from patients, 80% showed low level or no expression. To study the role of fibulin-1D in transformation, we transfected 6A/SB1 cells and a human fibrosarcoma-derived cell line (SHAC) with a fibulin-1D cDNA expression construct. Transfectants displaying high levels of fibulin-1D were isolated and characterized. Elevated expression of fibulin-1D led to reduced ability to form colonies in soft agar and reduced invasive potential as tested in a matrigel in vitro invasion assay. Furthermore, expression of fibulin-1D resulted in a markedly extended latency in tumor formation in athymic mice. These results indicate that low expression of fibulin-1D plays a role in tumor formation and invasion."xsd:string
http://purl.uniprot.org/citations/9393974http://purl.org/dc/terms/identifier"doi:10.1038/sj.onc.1201385"xsd:string
http://purl.uniprot.org/citations/9393974http://purl.org/dc/terms/identifier"doi:10.1038/sj.onc.1201385"xsd:string
http://purl.uniprot.org/citations/9393974http://purl.uniprot.org/core/author"Argraves W.S."xsd:string
http://purl.uniprot.org/citations/9393974http://purl.uniprot.org/core/author"Argraves W.S."xsd:string
http://purl.uniprot.org/citations/9393974http://purl.uniprot.org/core/author"Tran H."xsd:string
http://purl.uniprot.org/citations/9393974http://purl.uniprot.org/core/author"Tran H."xsd:string
http://purl.uniprot.org/citations/9393974http://purl.uniprot.org/core/author"Qing J."xsd:string
http://purl.uniprot.org/citations/9393974http://purl.uniprot.org/core/author"Qing J."xsd:string
http://purl.uniprot.org/citations/9393974http://purl.uniprot.org/core/author"Dunstan R.W."xsd:string
http://purl.uniprot.org/citations/9393974http://purl.uniprot.org/core/author"Dunstan R.W."xsd:string
http://purl.uniprot.org/citations/9393974http://purl.uniprot.org/core/author"Maher V.M."xsd:string
http://purl.uniprot.org/citations/9393974http://purl.uniprot.org/core/author"Maher V.M."xsd:string
http://purl.uniprot.org/citations/9393974http://purl.uniprot.org/core/author"McCormick J.J."xsd:string
http://purl.uniprot.org/citations/9393974http://purl.uniprot.org/core/author"McCormick J.J."xsd:string
http://purl.uniprot.org/citations/9393974http://purl.uniprot.org/core/date"1997"xsd:gYear
http://purl.uniprot.org/citations/9393974http://purl.uniprot.org/core/date"1997"xsd:gYear
http://purl.uniprot.org/citations/9393974http://purl.uniprot.org/core/name"Oncogene"xsd:string
http://purl.uniprot.org/citations/9393974http://purl.uniprot.org/core/name"Oncogene"xsd:string
http://purl.uniprot.org/citations/9393974http://purl.uniprot.org/core/pages"2159-2168"xsd:string
http://purl.uniprot.org/citations/9393974http://purl.uniprot.org/core/pages"2159-2168"xsd:string
http://purl.uniprot.org/citations/9393974http://purl.uniprot.org/core/title"Suppression of anchorage-independent growth and matrigel invasion and delayed tumor formation by elevated expression of fibulin-1D in human fibrosarcoma-derived cell lines."xsd:string
http://purl.uniprot.org/citations/9393974http://purl.uniprot.org/core/title"Suppression of anchorage-independent growth and matrigel invasion and delayed tumor formation by elevated expression of fibulin-1D in human fibrosarcoma-derived cell lines."xsd:string