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PMID: 2189108 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Lack of correlation between intercellular junctional communication, p21rasEJ expression, and spontaneous metastatic properties of rat mammary cells after transfection with c-H-rasEJ or neo genes.

Oncogene ·Vol. 5 ·No. 5 ·1990-05-00 ·Pages 747-53

Nicolson GL, Gallick GE, Dulski KM, Spohn WH, Lembo TM, Tainsky MA

Abstract

The loss of intercellular junctional communication between rat 13762NF mammary carcinoma cells and their spontaneous metastatic potentials from the mammary fat pad show a high degree of correlation. We examined a stable, benign, completely junctionally coupled cell clone (MTC.4) of this system after calcium phosphate-mediated transfection with c-H-rasEJ/pSV2neo and control pSV2neo-containing plasmids. There was a good correlation between the copy numbers of c-H-rasEJ incorporated into MTC.4 cells and their contents of p21rasEJ; however, there was not always a correspondence between spontaneous metastatic potential and copy number of c-H-rasEJ or amount of p21rasEJ. After c-H-rasEJ/pSV2neo transfection, some MTC.4 cells lost intercellular junctional communication and became spontaneously metastatic, although some nonmetastatic transfectants also had low percentages of junctionally coupled cells. One of the control pSV2neo transfectants also became metastatic and lost intercellular junctional coupling, and calcium phosphate treatment itself resulted in increased growth rates at mammary fat pad sites and a marginal increase in incidence of spontaneous metastases, both of which preceded loss of intercellular junctional coupling in some cells. Examination of 12 subclones derived from two cloned transfectants, however, revealed a poor correlation between spontaneous metastatic potential and intercellular junctional coupling. The results suggest that loss of junctional communication between cells is often but not always associated with the progression of cells from benign to metastatic states.

MeSH Terms
Animals Cell Communication/physiology Cell Line Drug Resistance, Microbial/genetics Female Gene Expression/physiology Intercellular Junctions/physiology Mammary Neoplasms, Experimental/genetics,pathology,physiopathology Neoplasm Metastasis/genetics,pathology Proto-Oncogene Proteins/genetics,physiology Proto-Oncogene Proteins p21(ras) Rats Transfection/genetics
Chemicals
Proto-Oncogene Proteins Proto-Oncogene Proteins p21(ras)
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Nicolson G L
Department of Tumor Biology, University of Texas M.D. Anderson Cancer Center, Houston 77030.
Gallick G E
Dulski K M
Spohn W H
Lembo T M
Tainsky M A
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
0950-9232
Published
1990-05-00
Pages
747-53
Language
English
Region
England
NLM ID
8711562
Subset
IM
Grants
NCI NIH HHS · R01-CA48210 · United States
NCI NIH HHS · R23-CA39803 · United States
NCI NIH HHS · R35-CA44352 · United States
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