Pancreatic cancer-derived exosomes promoted pancreatic stellate cells recruitment by pancreatic cancer

• Published in: Journal of Cancer Vol. 10; no. 18; pp. 4397 - 4407
• Main Authors: Zhang, Yue-Feng, Zhou, Yi-Zhao, Zhang, Bo, Huang, Shi-Fei, Li, Peng-Ping, He, Xiao-Man, Cao, Guo-Dong, Kang, Mu-Xing, Dong, Xin, Wu, Yu-Lian
• Format: Journal Article
• Language: English
• Published: Australia Ivyspring International Publisher Pty Ltd 01.01.2019; Ivyspring International Publisher
• Subjects: Antibodies; Cloning; Colorectal cancer; Laboratory animals; Metastasis; MicroRNAs; Pancreatic cancer; Proteins; Research Paper; United States > US; China; Germany; Pancreatic stellate cells (PSCs); Exosomes; Pancreatic cancer; Recruitment
• ISSN: 1837-9664; 1837-9664
• DOI: 10.7150/jca.27590

Cancer-associated fibroblasts (CAFs), which are an important component of the tumor microenvironment, have been identified in the blood circulation of patients with cancer metastasis, and metastatic cancer cells can recruit circulating CAFs. However, primary carcinoma sites usually regulate the behavior of metastatic cancer cells through exosomes. Here, we hypothesized that cancer-derived exosomes could enhance CAF recruitment. Exosomes secreted by pancreatic cancer cells (PANC-1 and MIA PaCa-2) were isolated and characterized. The ability of pancreatic cancer to recruit pancreatic stellate cells (PSCs) was assessed with Transwell assays and bioluminescent imaging in a mouse model , and the underlying molecular mechanism was also investigated. The results showed that pancreatic cancer cell-derived exosomes (Exo-Pan and Exo-Mia) promoted the pancreatic cancer recruitment of PSCs. This effect was mediated partially by the transfer of the exosomal protein Lin28B to the recipient cells to activate the Lin28B/let-7/HMGA2/PDGFB signaling pathway. These results suggested that exosomes derived from local cancer could promote the formation of distant metastases through transferring the exosomal protein Lin28B to the metastatic cancer cells.