TY - JOUR
T1 - Therapeutics target of CXCR4 and its downstream in peritoneal carcinomatosis of gastric cancer
AU - Koizumi, Keiichi
AU - Kato, Shinichiro
AU - Sakurai, Hiroaki
AU - Hashimoto, Isaya
AU - Yasumoto, Kazuo
AU - Saiki, Ikuo
PY - 2012/1/1
Y1 - 2012/1/1
N2 - Patients with advanced gastric carcinoma, especially peritoneal dissemination, have a poor prognosis. Various treatments have been used for peritoneal dissemination of gastric cancer, but there is no effective therapy for this condition. At present, similar proprieties of chemokines between trafficking of leukocytes during immune and inflammatory reactions and organ selective migration of cancer cells during metastasis are widely recognized. In particular, chemokine CXCL12 and its receptors CXCR4 are now known to play an important role in cancer progression. Recently, we reported for the first time that CXCR4 and its ligand, CXCL12, were involved in the development of peritoneal carcinomatosis of gastric cancer, and additionally, clarified the molecular mechanisms of the cell signaling pathways by which gastric cancer develops metastatic ability via CXCR4 and mTOR. In this review, we focus on the biological functions of chemokine receptors, particularly CXCR4 expressed on gastric cancer cells, and the therapeutic strategies targeting CXCR4-mediating signaling pathways in peritoneal carcinomatosis.
AB - Patients with advanced gastric carcinoma, especially peritoneal dissemination, have a poor prognosis. Various treatments have been used for peritoneal dissemination of gastric cancer, but there is no effective therapy for this condition. At present, similar proprieties of chemokines between trafficking of leukocytes during immune and inflammatory reactions and organ selective migration of cancer cells during metastasis are widely recognized. In particular, chemokine CXCL12 and its receptors CXCR4 are now known to play an important role in cancer progression. Recently, we reported for the first time that CXCR4 and its ligand, CXCL12, were involved in the development of peritoneal carcinomatosis of gastric cancer, and additionally, clarified the molecular mechanisms of the cell signaling pathways by which gastric cancer develops metastatic ability via CXCR4 and mTOR. In this review, we focus on the biological functions of chemokine receptors, particularly CXCR4 expressed on gastric cancer cells, and the therapeutic strategies targeting CXCR4-mediating signaling pathways in peritoneal carcinomatosis.
KW - CXCR4
KW - Gastric cancer
KW - MTOR
KW - Peritoneal carcinomatosis
KW - Review
UR - http://www.scopus.com/inward/record.url?scp=84866098504&partnerID=8YFLogxK
U2 - 10.2741/s267
DO - 10.2741/s267
M3 - 学術論文
C2 - 22202059
AN - SCOPUS:84866098504
SN - 1945-0516
VL - 4 S
SP - 269
EP - 276
JO - Frontiers in Bioscience - Scholar
JF - Frontiers in Bioscience - Scholar
IS - 1
ER -