TY - JOUR
T1 - The role of gap junctions in inflammatory and neoplastic disorders (Review)
AU - Wong, Pui
AU - Laxton, Victoria
AU - Srivastava, Saurabh
AU - Fiona Chan, Yin Wah
AU - Tse, Gary
PY - 2017/3
Y1 - 2017/3
N2 - Gap junctions are intercellular channels made of connexin proteins, mediating both electrical and biochemical signals between cells. The ability of gap junction proteins to regulate immune responses, cell proliferation, migration, apoptosis and carcinogenesis makes them attractive therapeutic targets for treating inflammatory and neoplastic disorders in different organ systems. Alterations in gap junction profile and expression levels are observed in hyperproliferative skin disorders, lymphatic vessel diseases, inflammatory lung diseases, liver injury and neoplastic disorders. It is now recognized that the therapeutic effects mediated by traditional pharmacological agents are dependent upon gap junction communication and may even act by influencing gap junction expression or function. Novel strategies for modulating the function or expression of connexins, such as the use of synthetic mimetic peptides and siRNA technology are considered.
AB - Gap junctions are intercellular channels made of connexin proteins, mediating both electrical and biochemical signals between cells. The ability of gap junction proteins to regulate immune responses, cell proliferation, migration, apoptosis and carcinogenesis makes them attractive therapeutic targets for treating inflammatory and neoplastic disorders in different organ systems. Alterations in gap junction profile and expression levels are observed in hyperproliferative skin disorders, lymphatic vessel diseases, inflammatory lung diseases, liver injury and neoplastic disorders. It is now recognized that the therapeutic effects mediated by traditional pharmacological agents are dependent upon gap junction communication and may even act by influencing gap junction expression or function. Novel strategies for modulating the function or expression of connexins, such as the use of synthetic mimetic peptides and siRNA technology are considered.
KW - Cancer
KW - Connexins
KW - Gap junctions
KW - Inflammation
KW - Mimetic peptides
UR - http://www.scopus.com/inward/record.url?scp=85013071199&partnerID=8YFLogxK
U2 - 10.3892/ijmm.2017.2859
DO - 10.3892/ijmm.2017.2859
M3 - Review article
C2 - 28098880
AN - SCOPUS:85013071199
SN - 1107-3756
VL - 39
SP - 498
EP - 506
JO - International Journal of Molecular Medicine
JF - International Journal of Molecular Medicine
IS - 3
ER -