[논문]PLAG Exerts Anti-Metastatic Effects by Interfering with Neutrophil Elastase/PAR2/EGFR Signaling in A549 Lung Cancer Orthotopic Model

Kim, Guen Tae; Hahn, Kyu Woong; Yoon, Sun Young; Sohn, Ki-Young; Kim, Jae Wha

doi:10.3390/cancers12030560

[해외논문] PLAG Exerts Anti-Metastatic Effects by Interfering with Neutrophil Elastase/PAR2/EGFR Signaling in A549 Lung Cancer Orthotopic Model 원문보기

Cancers, v.12 no.3, 2020년, pp.560 -

Kim, Guen Tae (Korea Research Institute of Bioscience and Biotechnology, 125 Kwahak-ro, Daejeon 34141, Korea) , Hahn, Kyu Woong (kgt121@kribb.re.kr) , Yoon, Sun Young (Department of Biological Sciences, Hannam University, 1646 Daedeok-daero, Daejeon 34054, Korea) , Sohn, Ki-Young (ENZYCHEM life sciences, 10F aT Center 27 Gangnam-daero, Seoul 06774, Korea) , Kim, Jae Wha (syyoon@enzychem.com (S.Y.Y.))

Abstract ▼ AI-Helper

The effectiveness of chemotherapy and radiotherapy to treat lung cancer is limited because of highly metastatic nature. Novel strategies and drugs to attenuate metastatic activity are urgently required. In this study, red fluorescence proteins (RFP)-labeled A549 human lung cancer cells were orthotopically implantation, where they developed primary tumors. Metastasis in brain and intestines were reduced by up to 80% by treatment with 100 mpk 1-palmitoyl-2-linoleoyl-3-acetyl-rac-glycerol (PLAG) compared with that in control mice. PLAG treatment also reduced the migration of the primary tumors. Interestingly, substantial neutrophil infiltration was observed in the tumors in control mice. The neutrophil contribution to A549 cell metastatic activity was examined in in vitro co-culture system. Metastatic activity could be achieved in the A549 cells through epidermal growth factor receptor (EGFR) transactivation mediated by protease activating receptor 2 (PAR2) receptor. Neutrophil elastase secreted from tumor-infiltrating neutrophils stimulated PAR2 and induced EGFR transactivation. However, this transactivation was inhibited by inducing PAR2 degradation following PLAG treatment and metastatic activity was effectively inhibited. PLAG attenuated cancer metastatic activity via modulated PAR2/EGFR transactivation by accelerating PAR2 degradation. These results suggest PLAG as potential therapeutic agent to combat tumor metastasis via regulating the activation signal pathway of PAR2 by tumor infiltrate-neutrophils.

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