EF24 Suppresses Invasion and Migration of Hepatocellular Carcinoma CellsIn Vitrovia Inhibiting the Phosphorylation of Src

Author:

Zhao Ran1ORCID,Tin Lamtin2,Zhang Yuhua1ORCID,Wu Yiqi1,Jin Yinji1,Jin Xiaoming1,Zhang Fengmin3,Li Xiaobo145ORCID

Affiliation:

1. Department of Pathology, Harbin Medical University, Harbin, Heilongjiang 150081, China

2. Department of Hepatopancreatobiliary Surgery, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266071, China

3. Department of Microbiology, Harbin Medical University, Harbin, Heilongjiang 150081, China

4. Translation Medicine Center of Northern China, Harbin Medical University, Harbin, Heilongjiang 150081, China

5. Basic Medical Institute, Heilongjiang Medical Science Academy, Heilongjiang 150081, China

Abstract

Diphenyl difluoroketone (EF24), a curcumin analog, is a promising anticancer compound that exerts its effects by inhibiting cell proliferation and inducing apoptosis. However, the efficacy of EF24 against cancer metastasis, particularly in hepatocellular carcinoma (HCC), remains elusive. In this study, the effect of EF24 on HCCLM-3 and HepG2 cell migration and invasion was detected by wound healing and transwell assay, respectively. The results revealed that EF24 suppressed the migration and invasion of both HCCLM-3 and HepG2 cells. Furthermore, EF24 treatment decreased the formation of filopodia on the cell surface and inhibited the phosphorylation of Src in both cell lines, which may help contribute towards understanding the mechanism underlying the suppressive effect of EF24 on HCC migration and invasion. Additionally, the expression of total- and phosphorylated-Src in primary HCC tissues and their paired lymph node metastatic tissues was detected, and phosphorylated-Src was found to be associated with HCC lymph node metastasis. The results of this study suggest that Src is a novel and promising therapeutic target in HCC and provide evidence to support the hypothesis that EF24 may be a useful therapeutic agent for the treatment of HCC.

Funder

Postdoctoral Scientific Research Development Fund

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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