Literature DB >> 8048793

The role of gap junctional intercellular communication in neoplasia.

R J Ruch1.   

Abstract

Gap junctions are comprised of proteinaceous, plasma membrane channels that link the interiors of adjacent cells and permit cells to directly exchange small (< 1,000 Daltons) molecules and ions. This exchange, termed gap junctional intercellular communication (GJIC), appears to be involved in growth regulation. Growth controlling factors may pass between cells through the junctions. The loss of gap junctions or impairment of their permeability has been observed in many neoplastic cells and cells treated with growth promoting carcinogens and other agents. The loss of GJIC appears to be an important event in the conversion of a normal cell into a neoplastic one. On the other hand, the restoration of GJIC in neoplastic cells by transfection with gap junction protein (connexin) cyclic deoxyribonucleic acids (cDNAs) or by stimulating endogenous connexin gene expression has led to the reversal of the neoplastic phenotype. The biology of gap junctions and their role in growth regulation and neoplasia are reviewed.

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Year:  1994        PMID: 8048793

Source DB:  PubMed          Journal:  Ann Clin Lab Sci        ISSN: 0091-7370            Impact factor:   1.256


  12 in total

1.  Androgen-regulated formation and degradation of gap junctions in androgen-responsive human prostate cancer cells.

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Journal:  Mol Biol Cell       Date:  2006-10-18       Impact factor: 4.138

2.  Role of connexin 43 in the maintenance of spontaneous activity in the guinea pig prostate gland.

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Journal:  Br J Pharmacol       Date:  2010-12       Impact factor: 8.739

Review 3.  Molecular mechanisms of glioma cell migration and invasion.

Authors:  Tim Demuth; Michael E Berens
Journal:  J Neurooncol       Date:  2004-11       Impact factor: 4.130

4.  Dexamethasone differentially regulates functional membrane properties in glioma cell lines and primary astrocytes in vitro.

Authors:  Daniel Hinkerohe; Dörte Wolfkühler; Aiden Haghikia; Carola Meier; Pedro M Faustmann; Uwe Schlegel
Journal:  J Neurooncol       Date:  2010-11-24       Impact factor: 4.130

5.  Treatment with connexin 46 siRNA suppresses the growth of human Y79 retinoblastoma cell xenografts in vivo.

Authors:  Diana B Burr; Samuel A Molina; Debarshi Banerjee; Derek M Low; Dolores J Takemoto
Journal:  Exp Eye Res       Date:  2011-02-12       Impact factor: 3.467

6.  A potential role of connexin 43 in epidermal growth factor-induced proliferation of mouse embryonic stem cells: involvement of Ca2+/PKC, p44/42 and p38 MAPKs pathways.

Authors:  J H Park; M Y Lee; J S Heo; H J Han
Journal:  Cell Prolif       Date:  2008-10       Impact factor: 6.831

7.  The anticancer effect of PQ1 in the MMTV-PyVT mouse model.

Authors:  Stephanie N Shishido; Adélaïde Delahaye; Amanda Beck; Thu Annelise Nguyen
Journal:  Int J Cancer       Date:  2013-09-19       Impact factor: 7.396

8.  Glomerular expression of connexin 40 and connexin 43 in rat experimental glomerulonephritis.

Authors:  Tetsuo Morioka; Shinichi Okada; Masaaki Nameta; Fadia Kamal; Nadia T Yanakieva-Georgieva; Jian Yao; Ayako Sato; Honglan Piao; Takashi Oite
Journal:  Clin Exp Nephrol       Date:  2012-09-04       Impact factor: 2.801

9.  Bovine herpesvirus tegument protein VP22 enhances thymidine kinase/ganciclovir suicide gene therapy for neuroblastomas compared to herpes simplex virus VP22.

Authors:  Zhaohua Qiu; Jerome S Harms; Jun Zhu; Gary A Splitter
Journal:  J Virol       Date:  2004-04       Impact factor: 5.103

Review 10.  Models and methods for in vitro testing of hepatic gap junctional communication.

Authors:  Michaël Maes; Sara Crespo Yanguas; Joost Willebrords; Mathieu Vinken
Journal:  Toxicol In Vitro       Date:  2015-09-28       Impact factor: 3.500

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