Reference SummaryRuch RJ, Exp Lung Res 2001 Apr-May;27(3):231-43
Title |
Defective gap junctional intercellular communication in lung cancer: loss of an important mediator of tissue homeostasis and phenotypic regulation. |
Authors |
Ruch RJ; Porter S; Koffler LD; Dwyer-Nield LD; Malkinson AM |
Journal |
Exp Lung Res |
Volume |
27 |
Issue |
3 |
Year |
2001 |
Pages |
231-43 |
Abstract |
Gap junctions provide direct pathways for the exchange of molecules and ions between neighboring cells, a process known as gap junctional intercellular communication (GJIC). This GJIC is important for homeostasis and regulation of mitosis, differentiation, and apoptosis. Gap junctions are present in lung airway and alveolar epithelial cells and, in addition to the above roles, might coordinate ciliary beating and surfactant secretion. GJIC is decreased in human and mouse lung carcinoma cells because of reduced expression of the gap junction protein, connexin43 (Cx43), and defects in signal transduction pathways that mediate Cx43 function. This reduced GJIC is important in the behavior of lung carcinoma cells because forced expression of Cx43 in lung carcinoma cells inhibits their growth and tumorigenicity. In this report, we summarize our studies on the role of GJIC in lung neoplasia. |
Links |
J:68461 – MGI References 11293326 – National Library of Medicine/PubMed |
| Strain | Model Name | Treatment Agent(s) | Organ Affected | Frequency | Model Details |
|---|---|---|---|---|---|
| A/J | Lung adenoma |
|
Lung |
observed |
|
| A/J | Lung carcinoma |
|
Lung |
observed |