» Articles » PMID: 15349812

Transcriptional Regulation of Cadherins During Development and Carcinogenesis

Overview
Journal Int J Dev Biol
Date 2004 Sep 7
PMID 15349812
Citations 211
Authors
Affiliations
Soon will be listed here.
Abstract

The cadherin superfamily of Ca(2+)-dependent homophilic adhesion molecules plays a critical role in regulating cell-to-cell interactions. During development, the expression of different cadherins is highly dynamic, since they are associated with the morphogenesis, establishment and/or maintenance of different tissues. Alterations in cadherin expression or function occur frequently during carcinogenesis, such as the loss of the epithelial cadherin (E-cadherin) and/or the aberrant expression of other cadherins. Indeed, the aberrant expression of cadherins has been detected during carcinoma invasion, a process which is reminiscent of the epithelial-mesenchymal transition (EMT) so important in many critical developmental processes. The functional regulation of cadherins can occur at many different levels, from transcriptional regulation to the control of the strength of the cadherin-mediated cell-cell interaction. In this review, we will focus on the transcriptional control of cadherin expression, both in development and carcinogenesis, paying particular attention to the regulation of E-cadherin given its proposed role as a suppressor of invasion. We will discuss the main genetic and epigenetic mechanisms involved in down-regulating E-cadherin expression, and we will analyse the mechanisms involved in regulating EMT, in an attempt to elucidate which elements are common to this process in both physiological and pathological situations.

Citing Articles

Conventional techniques and emerging nanotechnologies for early detection of cancer metastasis via epithelial-mesenchymal transition monitoring.

Zhang Z, Wang J, Wuethrich A, Trau M Natl Sci Rev. 2025; 12(3):nwae452.

PMID: 39926198 PMC: 11804803. DOI: 10.1093/nsr/nwae452.


In Silico Evaluation of Some Computer-Designed Fluoroquinolone-Glutamic Acid Hybrids as Potential Topoisomerase II Inhibitors with Anti-Cancer Effect.

Oancea O, Gaz S, Marc G, Lungu I, Rusu A Pharmaceuticals (Basel). 2025; 17(12.

PMID: 39770435 PMC: 11679884. DOI: 10.3390/ph17121593.


Senescent cells promote breast cancer cells motility by secreting GM-CSF and bFGF that activate the JNK signaling pathway.

Wang N, Fang Y, Hou Y, Cheng D, Dressler E, Wang H Cell Commun Signal. 2024; 22(1):478.

PMID: 39375718 PMC: 11457416. DOI: 10.1186/s12964-024-01861-x.


Competing endogenous RNAs regulatory crosstalk networks: The messages from the RNA world to signaling pathways directing cancer stem cell development.

Aria H, Azizi M, Nazem S, Mansoori B, Darbeheshti F, Niazmand A Heliyon. 2024; 10(15):e35208.

PMID: 39170516 PMC: 11337742. DOI: 10.1016/j.heliyon.2024.e35208.


TGF-β Modulated Pathways in Colorectal Cancer: New Potential Therapeutic Opportunities.

Fasano M, Pirozzi M, Miceli C, Cocule M, Caraglia M, Boccellino M Int J Mol Sci. 2024; 25(13).

PMID: 39000507 PMC: 11242595. DOI: 10.3390/ijms25137400.