生物
肺癌
癌变
中性粒细胞胞外陷阱
刘易斯肺癌
细胞外
癌基因
癌症研究
癌症
肿瘤坏死因子α
细胞因子
肺
癌细胞
免疫学
病理
炎症
细胞生物学
细胞周期
医学
内科学
转移
遗传学
作者
Yan Li,Yonglin Yang,Tingting Gan,Jiawei Zhou,Fan Hu,Nannan Hao,Baorui Yuan,Yu Chen,Mingshun Zhang
标识
DOI:10.3892/ijo.2019.4808
摘要
Neutrophil infiltration is frequently observed in lung cancer tissues. Extracellular RNAs (exRNAs) may facilitate tumor progression. The present study investigated the cross‑talk of tumor exRNAs and neutrophil extracellular traps (NETs) in lung cancer. Lewis lung carcinoma (LLC) cells were cultured with the deprived sera. And the cell culture supernatants (CCS) were analyzed in vitro and in vivo. The results revealed that exRNAs from lung cancer CCS promoted the inflammatory cytokine interleukin‑1β and reduced the vascular cell adhesion molecule‑1 expression in lung epithelial cells. Lung cancer CCS‑treated epithelial cells induced the production of NETs. By contrast, NETs reduced the tight junction protein claudin‑5 in epithelial cells. Furthermore, NETs caused the necrosis of epithelial cells, which resulted in the release of exRNAs. In mice, lung cancer cells instilled in the lung recruited neutrophils and initiated NETs. In patients with lung cancer, NETs were also observed. These results suggested that exRNAs in the cell culture supernatant may indirectly induce NETs and contribute to lung cancer oncogenesis.
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