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多瘤病毒中T抗原基因与人c-myc癌基因在大鼠甲状腺上皮分化细胞系中的合作:体外进展模型

Cooperation between the polyomavirus middle-T-antigen gene and the human c-myc oncogene in a rat thyroid epithelial differentiated cell line: model of in vitro progression.

作者信息

Berlingieri M T, Portella G, Grieco M, Santoro M, Fusco A

机构信息

Dipartimento di Biologia e Patologia Cellulare e Molecolare, II Facoltà di Medicina e Chirurgia, Università di Napoli, Italy.

出版信息

Mol Cell Biol. 1988 May;8(5):2261-6. doi: 10.1128/mcb.8.5.2261-2266.1988.

DOI:10.1128/mcb.8.5.2261-2266.1988
PMID:2838744
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC363414/
Abstract

Two rat thyroid epithelial differentiated cell lines, PC Cl 3 and PC myc, were infected with the polyoma murine leukemia virus (PyMLV) carrying the Middle-T-antigen gene of polyomavirus. After infection, both cell lines acquired the typical markers of neoplastic transformation; however, the PC myc cells showed a greater malignant phenotype. Furthermore, the thyroid differentiated functions were completely suppressed in PC myc cells transformed by PyMLV, whereas they were, at least partially, retained in PC Cl 3 cells transformed by PyMLV, and in particular, thyroglobulin synthesis and secretion were not affected at all. Since no differences in the expression of the middle-T-antigen gene were observed in the two PyMLV-transformed cell lines, the different properties shown by these two infected cell lines must be ascribed to the expression of the c-myc oncogene.

摘要

两种大鼠甲状腺上皮分化细胞系,PC Cl 3和PC myc,被携带多瘤病毒中间T抗原基因的多瘤小鼠白血病病毒(PyMLV)感染。感染后,两种细胞系都获得了肿瘤转化的典型标志物;然而,PC myc细胞表现出更大的恶性表型。此外,PyMLV转化的PC myc细胞中甲状腺分化功能被完全抑制,而在PyMLV转化的PC Cl 3细胞中,该功能至少部分得以保留,特别是甲状腺球蛋白的合成和分泌完全不受影响。由于在两种PyMLV转化的细胞系中未观察到中间T抗原基因表达的差异,这两种感染细胞系所表现出的不同特性必定归因于c-myc癌基因的表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d25/363414/95dff6076071/molcellb00065-0415-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d25/363414/faee17fb013b/molcellb00065-0412-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d25/363414/3d29e6982ff1/molcellb00065-0414-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d25/363414/5c747117d442/molcellb00065-0415-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d25/363414/0989a7f08cd5/molcellb00065-0415-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d25/363414/95dff6076071/molcellb00065-0415-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d25/363414/faee17fb013b/molcellb00065-0412-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d25/363414/3d29e6982ff1/molcellb00065-0414-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d25/363414/5c747117d442/molcellb00065-0415-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d25/363414/0989a7f08cd5/molcellb00065-0415-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d25/363414/95dff6076071/molcellb00065-0415-c.jpg

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