Literature DB >> 3986803

Phorbol ester-mediated inhibition of intercellular communication in BALB/c 3T3 cells: relationship to enhancement of cell transformation.

T Enomoto, H Yamasaki.   

Abstract

Tumor-promoting phorbol esters reversibly inhibit intercellular communication between BALB/c 3T3 cells. In order to study the possible role of blocked intercellular communication in the promotion step in cell transformation, we investigated the effect of phorbol ester tumor promoters on cell transformation and intercellular communication in BALB/c 3T3 A31-1-1 cells by a dye-transfer method. When the cells are in the growing phase, inhibition of dye transfer by phorbol esters is complete but transient; more than 90% inhibition was observed 4 h after treatment of the cells with either 12-O-tetradecanoylphorbol-13-acetate or phorbol-12,13-didecanoate, but the extent of dye transfer returned to the control level after 24 h of treatment. However, when these phorbol ester-treated cells were cultured beyond confluence in the presence of tumor promoters, the capacity to transfer dye decreased again and was inhibited continuously for at least 5 weeks of culture. In control cultures, the extent of dye transfer between cells did not decrease at their confluence. The ability of 12-O-tetradecanoylphorbol-13-acetate and phorbol-12,13-didecanoate to induce continuous inhibition of dye transfer between these cells correlated well with their capacity to promote transformation of BALB/c 3T3 cells initiated with 20-methylcholanthrene. These results suggest that the continuously blocked intercellular communication after confluence, rather than its transient inhibition during the growing phase, might play an important role in the promotion of in-vitro two-stage transformation of BALB/c 3T3 cells.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 3986803

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


  11 in total

1.  Inhibition of intercellular communication by airborne particulate matter.

Authors:  G A Heussen
Journal:  Arch Toxicol       Date:  1991       Impact factor: 5.153

2.  Characterization of the progressive sublines derived from a weakly malignant cloned cell line, ER-1, co-inoculated subcutaneously with a foreign body.

Authors:  J Hamada; H Nagayasu; T Kawano; T Mizutani; D Nakata; M Hosokawa; N Takeichi
Journal:  Clin Exp Metastasis       Date:  1998-04       Impact factor: 5.150

3.  Characterization of a rat liver epithelial cell line to detect inhibitors of metabolic cooperation.

Authors:  C Jone; J E Trosko; C C Chang
Journal:  In Vitro Cell Dev Biol       Date:  1987-03

4.  Effects of tumor promoters, genotoxic carcinogens and hepatocytotoxins on mouse hepatocyte intercellular communication.

Authors:  R J Ruch; J E Klaunig
Journal:  Cell Biol Toxicol       Date:  1986-12       Impact factor: 6.691

5.  Phosphorylation of MP26, a lens junction protein, is enhanced by activators of protein kinase C.

Authors:  P D Lampe; R G Johnson
Journal:  J Membr Biol       Date:  1989-02       Impact factor: 1.843

6.  SRC points the way to biomarkers and chemotherapeutic targets.

Authors:  Harini Krishnan; W Todd Miller; Gary S Goldberg
Journal:  Genes Cancer       Date:  2012-05

7.  Phosphatidylinositol-bisphosphate regulates intercellular coupling in cardiac myocytes.

Authors:  Johannes P Hofgaard; Kathrin Banach; Sarah Mollerup; Helene Korvenius Jørgensen; Søren Peter Olesen; Niels-Henrik Holstein-Rathlou; Morten Schak Nielsen
Journal:  Pflugers Arch       Date:  2008-06-07       Impact factor: 3.657

Review 8.  Multistage carcinogenesis: implications for risk estimation.

Authors:  H Yamasaki
Journal:  Cancer Metastasis Rev       Date:  1988-04       Impact factor: 9.264

9.  Identification of tumor promoters by their inhibitory effect on intercellular transfer of lucifer yellow.

Authors:  I V Budunova; L A Mittelman; G A Belitsky
Journal:  Cell Biol Toxicol       Date:  1989-01       Impact factor: 6.691

Review 10.  Aberrant expression and function of gap junctions during carcinogenesis.

Authors:  H Yamasaki
Journal:  Environ Health Perspect       Date:  1991-06       Impact factor: 9.031

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.