Literature DB >> 2647289

Suppression of tumorigenicity in human cell hybrids derived from cell lines expressing different activated ras oncogenes.

A G Geiser1, M J Anderson, E J Stanbridge.   

Abstract

Four different human tissue-derived cell lines, each previously shown to express either a Ha-, Ki-, or N-ras-activated oncogene, were fused in four different paired combinations. The three combinations that involved the tumor line HT1080 (activated N-ras oncogene) were found to be tumorigenic in nude mice, but to different degrees. However, the fusion of the tumor lines EJ and SW480 (activated Ha-ras and Ki-ras, respectively) resulted in hybrid cells suppressed for tumorigenicity. The EJ x SW480 hybrids were found to harbor and express both of the activated ras oncogenes. The results suggest that tumorigenic suppression can occur in the presence of two transforming oncogenes of the ras family and that tumorigenicity associated with ras oncogene activation involves additional mechanisms that may differ among tumor cells.

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Year:  1989        PMID: 2647289

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  5 in total

1.  Suppression of the progression phenotype in somatic cell hybrids occurs in the absence of altered adenovirus type 5 gene expression.

Authors:  G J Duigou; L E Babiss; D S Iman; J W Shay; P B Fisher
Journal:  Mol Cell Biol       Date:  1990-05       Impact factor: 4.272

2.  Progression of colorectal cancer is associated with multiple tumor suppressor gene defects but inhibition of tumorigenicity is accomplished by correction of any single defect via chromosome transfer.

Authors:  M C Goyette; K Cho; C L Fasching; D B Levy; K W Kinzler; C Paraskeva; B Vogelstein; E J Stanbridge
Journal:  Mol Cell Biol       Date:  1992-03       Impact factor: 4.272

3.  Identification of the HeLa tumor-associated antigen, p75/150, as intestinal alkaline phosphatase and evidence for its transcriptional regulation.

Authors:  K M Latham; E J Stanbridge
Journal:  Proc Natl Acad Sci U S A       Date:  1990-02       Impact factor: 11.205

4.  Role of non-genomic androgen signalling in suppressing proliferation of fibroblasts and fibrosarcoma cells.

Authors:  G Castoria; P Giovannelli; M Di Donato; A Ciociola; R Hayashi; F Bernal; E Appella; F Auricchio; A Migliaccio
Journal:  Cell Death Dis       Date:  2014-12-04       Impact factor: 8.469

5.  Novel Suppressive Effects of Ketotifen on Migration and Invasion of MDA-MB-231 and HT-1080 Cancer Cells.

Authors:  Hyun Ji Kim; Mi Kyung Park; Soo Youl Kim; Chang Hoon Lee
Journal:  Biomol Ther (Seoul)       Date:  2014-11-30       Impact factor: 4.634

  5 in total

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