TY - JOUR
T1 - Antagonism of the ATP-gated P2X7 receptor
T2 - a potential therapeutic strategy for cancer
AU - Drill, Matthew
AU - Jones, Nigel C.
AU - Hunn, Martin
AU - O’Brien, Terence J.
AU - Monif, Mastura
PY - 2021/6
Y1 - 2021/6
N2 - The P2X receptor 7 (P2X7R) is a plasma membrane receptor sensing extracellular ATP associated with a wide variety of cellular functions. It is most commonly expressed on immune cells and is highly upregulated in a number of human cancers where it can play a trophic role in tumorigenesis. Activation of this receptor leads to the formation of a non-selective cation channel, which has been associated with several cellular functions mediated by the PI3K/Akt pathway and protein kinases. Due to its broad range of functions, the receptor represents a potential therapeutic target for a number of cancers. This review describes the range of mechanisms associated with P2X7R activation in cancer settings and highlights the potential of targeted inhibition of P2X7R as a therapy. It also describes in detail a number of key P2X7R antagonists currently in pre-clinical and clinical development, including oxidised ATP, Brilliant Blue G (BBG), KN-62, KN-04, A740003, A438079, GSK1482160, CE-224535, JNJ-54175446, JNJ-55308942, and AZ10606120. Lastly, it summarises the in vivo studies and clinical trials associated with the use and development of these P2X7R antagonists in different disease contexts.
AB - The P2X receptor 7 (P2X7R) is a plasma membrane receptor sensing extracellular ATP associated with a wide variety of cellular functions. It is most commonly expressed on immune cells and is highly upregulated in a number of human cancers where it can play a trophic role in tumorigenesis. Activation of this receptor leads to the formation of a non-selective cation channel, which has been associated with several cellular functions mediated by the PI3K/Akt pathway and protein kinases. Due to its broad range of functions, the receptor represents a potential therapeutic target for a number of cancers. This review describes the range of mechanisms associated with P2X7R activation in cancer settings and highlights the potential of targeted inhibition of P2X7R as a therapy. It also describes in detail a number of key P2X7R antagonists currently in pre-clinical and clinical development, including oxidised ATP, Brilliant Blue G (BBG), KN-62, KN-04, A740003, A438079, GSK1482160, CE-224535, JNJ-54175446, JNJ-55308942, and AZ10606120. Lastly, it summarises the in vivo studies and clinical trials associated with the use and development of these P2X7R antagonists in different disease contexts.
KW - Antagonists
KW - Cancer
KW - Inflammation
KW - P2X7 receptor
KW - Purinergic receptors
UR - http://www.scopus.com/inward/record.url?scp=85102931514&partnerID=8YFLogxK
U2 - 10.1007/s11302-021-09776-9
DO - 10.1007/s11302-021-09776-9
M3 - Review Article
C2 - 33728582
AN - SCOPUS:85102931514
SN - 1573-9538
VL - 17
SP - 215
EP - 227
JO - Purinergic Signalling
JF - Purinergic Signalling
IS - 2
ER -