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shRNA targeting HDGF suppressed cell growth and invasion of squamous cell lung cancer
Jie Meng1, Wei Xie, Liming Cao
1Department of Respiratory Medicine, Xiangya Hospital, Central South University, Changsha, China.
Abstract:
Hepatoma-derived growth factor (HDGF), a nuclear protein with both mitogenic and angiogenic activity, has been reported to be mainly involved in tumorigenesis and the progression of non-small cell lung cancer. In this study, the HDGF expression was knocked down by specific-shRNA with lentivirus expression vector targeting HDGF in lung squamous cell carcinoma 520 cells. HDGF knocked down by shRNA suppressed the cell proliferation significantly both in vitro and in vivo as indicated by MTT, plate clone and transplanted tumor model assays. In addition, the knocked-down expression of HDGF also inhibited cell migration and invasion as shown in transwell and Boyden experiments. We concluded that HDGF acts as an oncogene participating in the pathogenesis of squamous cell lung cancer, and HDGF may be a key therapeutic target for non-small cell lung cancer.
Insights
Hepatoma-derived growth factor (HDGF) acts as an oncogene in lung cancer. Knocking down HDGF suppressed tumor cell proliferation, migration, and invasion, suggesting it as a therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Hepatoma-derived growth factor (HDGF) is a nuclear protein implicated in tumorigenesis.
- HDGF exhibits mitogenic and angiogenic activities, contributing to cancer progression, particularly in non-small cell lung cancer.
Purpose of the Study:
- To investigate the role of HDGF in lung squamous cell carcinoma.
- To evaluate the therapeutic potential of targeting HDGF in non-small cell lung cancer.
Main Methods:
- HDGF expression was suppressed using specific short hairpin RNA (shRNA) delivered via lentivirus in lung squamous cell carcinoma 520 cells.
- Cell proliferation was assessed using MTT, plate clone assays, and a transplanted tumor model.
- Cell migration and invasion were evaluated using transwell and Boyden assays.
Main Results:
- Knockdown of HDGF significantly inhibited cell proliferation both in vitro and in vivo.
- Suppression of HDGF expression reduced cell migration and invasion capabilities.
- HDGF was confirmed to promote proliferation, migration, and invasion in lung squamous cell carcinoma.
Conclusions:
- HDGF functions as an oncogene in the pathogenesis of squamous cell lung cancer.
- HDGF represents a potential therapeutic target for non-small cell lung cancer treatment.
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