4.6 Article

PAK3 promotes the metastasis of hepatocellular carcinoma by regulating EMT process

期刊

JOURNAL OF CANCER
卷 13, 期 1, 页码 153-161

出版社

IVYSPRING INT PUBL
DOI: 10.7150/jca.61918

关键词

PAK3; HCC; EMT; smad

类别

资金

  1. National Natural Science Foundation of China [82073373]
  2. Natural Science Foundation of Guangxi Province of China [{2015}57]
  3. National 10,000-person Program for Leading Talents in Scientific and Technological Innovation, Hundred talents plan for colleges and universities in Guangxi to introduce overseas high-level talents
  4. Scientific and Technological Innovation Major Base of Guangxi [2018-15-Z04]
  5. State Project for Essential Drug Research and Development [2019ZX09301132]
  6. Guangxi Key Research and Development Project [AB20117001]
  7. Guangxi science and technology bases and talent special project [AD17129062]

向作者/读者索取更多资源

This study found that PAK3 is highly expressed in HCC patients and is positively correlated with tumor stage and grade. PAK3 promotes the proliferation, migration, and invasion of HCC cells and regulates EMT-related molecules and pathways. Therefore, PAK3 may be a potential therapeutic target for HCC.
Purpose: Hepatocellular carcinoma (HCC) is one of the most common malignant tumors. The malignant biological behavior of HCC is closely related to epithelial-mesenchymal transition (EMT), and EMT plays an important role in the progression, migration and metastasis of HCC. P21-activated kinase 3 (PAK3) is a serine/threonine protein kinase, and PAK3 affects the EMT, proliferation, metastasis and invasion of HCC. Methods: In this study, the relationship between PAK3 and HCC was first analyzed by bioinformatics, and then, the expression of PAK3 in clinical samples was detected by immunohistochemistry (IHC), quantitative real-time PCR (qRT-PCR) and Western blotting. Subsequently, the expression of PAK3 was further confirmed in HCC cells. In addition, after the overexpression or knockdown of PAK3 in cells, the proliferation, migration and invasion abilities of these cells were assessed by Cell Counting Kit-8 (CCK-8), wound healing and Transwell assays, and the results were confirmed in vivo experiments in mice. In addition, we also verified that PAK3 affected the EMT and EMT-related pathway of HCC through qRT-PCR, Western blotting and immunofluorescence experiments. Results: Through database analysis, we found that PAK3 was highly expressed in HCC patients and was positively correlated with tumor stage and grade, suggesting that PAK3 expression was closely related to HCC occurrence and development. We subsequently confirmed that PAK3 was overexpressed in HCC clinical samples and HCC cell lines and that PAK3 promoted the proliferation, migration and invasion of HCC cells in vitro. Finally, we found that PAK3 regulated EMT-related molecule expression and EMT-related TGF-beta/smad signaling pathway. Conclusion: High expression of PAK3 enhances the invasion of HCC and regulates EMT, suggesting that PAK3 may be a potential target for the treatment of HCC.

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