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Clinical Significance of Combined Epithelial-Mesenchymal Transition Markers Expression and Role of Rac1 in Hepatocellular Carcinomaopen access

Authors
Shin, Seung KakRyu, SujinNam, SeungyoonHa, Seung YeonKwon, Oh SangKim, Yun SooKim, Se-HeeKim, Ju Hyun
Issue Date
Jan-2023
Publisher
MDPI
Keywords
hepatocellular carcinoma; epithelial-mesenchymal transition; Rac1; Snail; p21-activated kinases 1
Citation
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, v.24, no.2
Journal Title
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Volume
24
Number
2
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/86979
DOI
10.3390/ijms24021765
ISSN
1661-6596
Abstract
Epithelial-mesenchymal transition (EMT) has been implicated in cancer progression, invasion, and metastasis. We aimed to evaluate the correlations between clinicopathological characteristics and EMT markers in patients with hepatocellular carcinoma (HCC) who underwent surgical resection and to identify the key regulator in EMT process. Fresh-frozen HCC tissues and adjacent nontumor liver tissues from 30 patients who underwent surgical resection were provided by the Gachon University Gil Medical Center Bio Bank. Human HCC cell lines, Hep3B, SNU449, and Huh7 cells were transfected with Rac1 siRNA and exposed to hypoxic conditions. The combined EMT markers expression (down-expression of E-cadherin and overexpression of p21-activated kinases 1 (PAK1)/Snail) by Western blot in HCC tissues when compared to adjacent nontumor liver tissues was significantly associated with macrovascular invasion (p = 0.021), microvascular invasion (p = 0.001), large tumor size (p = 0.021), and advanced tumor stage (p = 0.015). Patients with combined EMT markers expression showed early recurrence and poor overall survival. In vitro studies showed that Rac1 knockdown decreased the expression of EMT markers including PAK1 and Snail in hypoxia-induced Hep3B cells and suppressed the migration and invasion of hypoxia-induced HCC cells. Rac1 may be a potential therapeutic target for inhibition of EMT process through the inhibition of PAK1 and Snail in HCC.
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