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Expression and Critical Role of Interleukin Enhancer Binding Factor 2 in Hepatocellular Carcinoma
Shaobing Cheng1,2,3, Xu Jiang4, Chaofeng Ding5
1Department of Hepatobiliary Surgery, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China. showcheng@126.com.
Abstract:
Interleukin enhancer binding factor 2 (ILF2), a transcription factor, regulates cell growth by inhibiting the stabilization of mRNA. Currently, its role has gained recognition as a factor in the tumorigenic process. However, until now, little has been known about the detailed role ILF2 plays in hepatocellular carcinoma (HCC). In this study, we investigated the expression levels of ILF2 in HCC tissue with Western blot and immunohistochemical assays. To examine the effect of ILF2 on liver cancer cell growth and apoptosis, small interfering RNAs (siRNAs) targeting ILF2 were recombined to create lentiviral overexpression vectors. Our results showed higher expression levels of ILF2 mRNA and ILF2 protein in HCC tissue compared with matched peritumoral tissue. Expression of ILF2 may regulate cell growth and apoptosis in liver cancer cells via regulation of B-cell lymphoma 2 (Bcl-2), Bcl-2 related ovarian killer (Bok), Bcl-2-associated X protein (BAX), and cellular inhibitor of apoptosis 1 (cIAP1). Moreover, we inoculated nude mice with liver cancer cells to investigate the effect of ILF2 on tumorigenesis in vivo. As expected, a rapid growth was observed in cancer cells inoculated with a lentiviral vector coding Flag-ILF2 (Lenti-ILF2) compared with the control cells. Hence, these results promote a better understanding of ILF2's potential role as a therapeutic target in HCC.
Insights
Interleukin enhancer binding factor 2 (ILF2) is upregulated in hepatocellular carcinoma (HCC), promoting tumor growth. Targeting ILF2 may offer a new therapeutic strategy for liver cancer.
Area of Science:
- Molecular Biology
- Oncology
- Biochemistry
Background:
- Interleukin enhancer binding factor 2 (ILF2) is a transcription factor involved in mRNA stabilization and cell growth.
- ILF2's role in tumorigenesis is recognized, but its specific function in hepatocellular carcinoma (HCC) remains unclear.
Purpose of the Study:
- To investigate the expression levels and functional role of ILF2 in HCC.
- To explore ILF2's potential as a therapeutic target for liver cancer.
Main Methods:
- Western blot and immunohistochemical assays to determine ILF2 expression in HCC tissues.
- Lentiviral vectors with small interfering RNAs (siRNAs) to modulate ILF2 expression in liver cancer cells.
- In vivo tumorigenesis assays in nude mice using ILF2-overexpressing cancer cells.
Main Results:
- ILF2 mRNA and protein levels were significantly higher in HCC tissues compared to adjacent non-tumorous tissues.
- ILF2 expression influenced liver cancer cell growth and apoptosis, potentially through regulating Bcl-2, Bok, BAX, and cIAP1.
- In vivo studies demonstrated accelerated tumor growth in mice inoculated with ILF2-overexpressing cancer cells.
Conclusions:
- ILF2 is overexpressed in HCC and promotes tumor growth and progression.
- ILF2 plays a significant role in regulating cell growth and apoptosis in liver cancer.
- ILF2 represents a promising therapeutic target for hepatocellular carcinoma.
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