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Updated: Jan 1, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
RP11-81H3.2 Acts as an Oncogene via microRNA-490-3p Inhibition and Consequential Tankyrase 2 Up-Regulation in
1Department of Surgical Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710061, Shaanxi, China.
Background:
Hepatocellular carcinoma (HCC) is a serious threat to human lives and is usually diagnosed at the late stages. Recently, there has been a rapid advancement in the treatment options for HCC, but novel therapeutic targets are still needed, especially for precision medicine.
Aims:
We aimed to investigate the involvement of non-coding RNA RP11-81H3.2 in HCC.
Methods:
The expression of RP11-81H3.2 was examined in the blood samples of HCC patients, and in the human HCC cell lines, including HepG2, Smmc-7721, and Huh7. Cell proliferation was determined using the CCK-8 and EdU assay, and cell invasion and migration were determined using the transwell/wound healing assay. The effects of RP11-81H3.2 knockdown on in vivo tumor growth were evaluated utilizing the nude mice HepG2 tumor xenograft model.
Results:
Here, we have identified a long non-coding RNA, RP11-81H3.2, which is enriched in HCC and can promote its proliferation, migration, and invasion both in vitro and in vivo. In addition, our results showed that RP11-81H3.2 binds to and regulate miR-490-3p expression in the HCC cells. Moreover, we found that RP11-81H3.2 regulates the expression of TNKS2 via miR-490-3p. Further, we found that RP11-81H3.2 and miR-490-3p form a regulatory loop; the release of RP11-81H3.2 leads to the suppression of miR-490-3p expression, thus, further enhancing the expression of RP11-81H3.2.
Conclusions:
Our data have provided a novel target for the diagnosis and treatment of HCC, and sheds light on the lncRNA-miRNA regulatory nexus that can control the HCC related pathogenesis.
Insights
This study identifies long non-coding RNA RP11-81H3.2 as a promoter of hepatocellular carcinoma (HCC) progression. RP11-81H3.2 enhances HCC cell proliferation, migration, and invasion, offering a potential new target for HCC diagnosis and treatment.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Hepatocellular carcinoma (HCC) poses a significant global health threat, often diagnosed late.
- Current HCC treatments are advancing, yet novel therapeutic targets are crucial for precision medicine.
Purpose of the Study:
- To investigate the role of the long non-coding RNA RP11-81H3.2 in hepatocellular carcinoma (HCC).
Main Methods:
- Examined RP11-81H3.2 expression in HCC patient blood and cell lines (HepG2, Smmc-7721, Huh7).
- Assessed cell proliferation, invasion, and migration in vitro.
- Evaluated RP11-81H3.2 knockdown effects on tumor growth in a nude mouse xenograft model.
Main Results:
- RP11-81H3.2 was found to be enriched in HCC and promoted proliferation, migration, and invasion in vitro and in vivo.
- RP11-81H3.2 was shown to regulate miR-490-3p and TNKS2 expression in HCC cells.
- A regulatory feedback loop between RP11-81H3.2 and miR-490-3p was identified, enhancing RP11-81H3.2 expression.
Conclusions:
- RP11-81H3.2 represents a novel therapeutic and diagnostic target for HCC.
- The findings elucidate a lncRNA-miRNA regulatory axis involved in HCC pathogenesis.
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