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ESTABLISHMENT OF COMPUTERIZED RAT LIVER EPITHELIAL CELL PROTEIN DATABASE

ESTABLISHMENT OF COMPUTERIZED RAT LIVER EPITHELIAL CELL PROTEIN DATABASE
计算机化大鼠肝上皮细胞蛋白数据库的建立
批准号:
3838481
负责人:
P J WIRTH
金额:
$0.0万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
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英文摘要
Our computerized database of rat liver epithelial (RLE) cellular polypeptides (Wirth et al., Electrophoresis 1991;12:931-54) has now been expanded to include the analysis of cellular polypeptide alterations during aflatoxin B1 (AFB1)-, spontaneously-, and oncogene (v-Ha-ras, v- raf, and v-myc/v-raf)-induced transformation of RLE cells. Two- dimensional mapping of 35-S-methionine labeled whole cell lysate, cell free in vitro translation products and 32-P-orthophosphate labeled polypeptides revealed subsets of polypeptides specific for each transfor- mation modality. A specific subcellular location for each of the major transformation sensitive proteins was made. Significant alterations in the expression of the extracellular matrix protein, fibronectin, as well as tropomyosin (TM)- and intermediate filament (IF)-related polypeptides (vimentin, alpha, beta-tubulin, the cytokeratins, and actin) were observed among the various transformant cell lines. Analysis of TM expression in four individual AFB1-, and four spontaneously-induced as well as each of the oncogene transformed cell lines, indicated that five major TM (TM 1-5) isoforms were variably expressed in the various cell lines, including one polypeptide tentatively identified as TM6. Whereas alterations in TM expression appeared to be transformation specific, alterations in the individual IF polypeptides were related more to the differentiation state of the individual cell lines rather than to the transformation phenotype. Our results to date extend our earlier efforts toward the establishment of a comprehensive computerized database of RLE cellular proteins and demonstrates how such a database may serve as a useful resource for studies concerning the regulation of growth and differentiation as well as transformation of RLE cells.
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ALTERED POLYPEPTIDE EXPRESSION DURING MAMMARY CARCINOGENESIS
ANALYSIS OF POLYPEPTIDE CHANGES DURING CELLULAR DIFFERENTIATION
GROWTH RELATED SIGNAL TRANSDUCTION PATHWAYS IN CARCINOGENESIS
EARLY EVENTS IN CHEMICALLY INDUCED RAT HEPATOCARCINOGENESIS
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