TY - JOUR
T1 - PAI-1 secreted from metastatic ovarian cancer cells triggers the tumor-promoting role of the mesothelium in a feedback loop to accelerate peritoneal dissemination
AU - Peng, Yang
AU - Kajiyama, Hiroaki
AU - Yuan, Hong
AU - Nakamura, Kae
AU - Yoshihara, Masato
AU - Yokoi, Akira
AU - Fujikake, Kayo
AU - Yasui, Hiroaki
AU - Yoshikawa, Nobuhisa
AU - Suzuki, Shiro
AU - Senga, Takeshi
AU - Shibata, Kiyosumi
AU - Kikkawa, Fumitaka
N1 - Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2019/2/1
Y1 - 2019/2/1
N2 - The mesothelium, covered by a continuous monolayer of mesothelial cells, is the first protective barrier against metastatic ovarian cancer. However, mesothelial cells release tumor-promoting factors that accelerate the process of peritoneal metastasis. We identified cancer-associated mesothelial cells (CAMs) that had tumor-promoting potential. Here, we found that plasminogen activator inhibitor-1 (PAI-1) induced the formation of CAMs, after which CAMs increasingly secreted the oncogenic factors interleukin-8 (IL-8) and C-X-C motif chemokine ligand 5 (CXCL5), further promoting the metastasis of ovarian cancer cells in a feedback loop. After the formation of CAMs, PAI-1 activated the nuclear factor kappa B (NFκB) pathway in the CAMs, thus transcriptionally upregulating the expression of the downstream NFκB targets IL-8 and CXCL5. Moreover, PAI-1 correlated with peritoneal metastasis in ovarian cancer patients and indicated a poor prognosis. In both ex vivo and in vivo models, after PAI-1 expression was knocked down, the metastasis of ovarian cancer cells decreased significantly. Therefore, targeting PAI-1 may provide a potential target for future therapeutics to prevent the formation of CAMs and alleviate peritoneal metastasis in ovarian cancer patients.
AB - The mesothelium, covered by a continuous monolayer of mesothelial cells, is the first protective barrier against metastatic ovarian cancer. However, mesothelial cells release tumor-promoting factors that accelerate the process of peritoneal metastasis. We identified cancer-associated mesothelial cells (CAMs) that had tumor-promoting potential. Here, we found that plasminogen activator inhibitor-1 (PAI-1) induced the formation of CAMs, after which CAMs increasingly secreted the oncogenic factors interleukin-8 (IL-8) and C-X-C motif chemokine ligand 5 (CXCL5), further promoting the metastasis of ovarian cancer cells in a feedback loop. After the formation of CAMs, PAI-1 activated the nuclear factor kappa B (NFκB) pathway in the CAMs, thus transcriptionally upregulating the expression of the downstream NFκB targets IL-8 and CXCL5. Moreover, PAI-1 correlated with peritoneal metastasis in ovarian cancer patients and indicated a poor prognosis. In both ex vivo and in vivo models, after PAI-1 expression was knocked down, the metastasis of ovarian cancer cells decreased significantly. Therefore, targeting PAI-1 may provide a potential target for future therapeutics to prevent the formation of CAMs and alleviate peritoneal metastasis in ovarian cancer patients.
KW - Cancer-associated mesothelial cells
KW - Microenvironment
KW - Ovarian cancer
KW - Peritoneal metastasis
KW - Plasminogen activator inhibitor-1
UR - http://www.scopus.com/inward/record.url?scp=85056210634&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85056210634&partnerID=8YFLogxK
U2 - 10.1016/j.canlet.2018.10.027
DO - 10.1016/j.canlet.2018.10.027
M3 - Article
C2 - 30429105
AN - SCOPUS:85056210634
SN - 0304-3835
VL - 442
SP - 181
EP - 192
JO - Cancer Letters
JF - Cancer Letters
ER -