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Exploring the functional role of tRF-39-8HM2OSRNLNKSEKH9 in hepatocellular carcinoma
Tianxin Xu1, Jie Yuan2, Fei Song1
1Department of General Surgery, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong, China.
Abstract:
Hepatocellular carcinoma (HCC) is associated with high morbidity and mortality globally. tRNA-derived small RNAs (tsRNAs) have emerged as potential targets for cancer treatment. However, the specific impact of tsRNAs on HCC remains undiscovered. In this study, we aimed to investigate the biological significance of tsRNAs in HCC. First, we screened the differentially expressed tsRNAs in HCC tissues and normal tissues adjacent to the tumor (NAT) using high-throughput sequencing and the results showed that tRF-39-8HM2OSRNLNKSEKH9 was more highly expressed in HCC tissues than NATs. Agarose gel electrophoresis (AGE), nuclear-cytoplasmic separation assays and fluorescence in situ hybridization (FISH) were employed to assess the characterization of tRF-39-8HM2OSRNLNKSEKH9. The relationship between the expression of tRF-39-8HM2OSRNLNKSEKH9 and clinicopathological parameters was evaluated and we found that it was positively associated with tumor size. The cell counting kit-8 (CCK8) assay, colony formation assay and EdU staining assay were employed to investigate the role of tRF-39-8HM2OSRNLNKSEKH9 in the proliferation of HCC cells. Additionally, transwell assays demonstrated that overexpression of tRF-39-8HM2OSRNLNKSEKH9 could accelerate cell migration capability. Taken together, tRF-39-8HM2OSRNLNKSEKH9 was highly expressed in HCC cells, serum and tissues, and it may play an oncogenic role in HCC cells through interacting with downstream mRNA targets.
Insights
This study identifies tRF-39-8HM2OSRNLNKSEKH9 as a highly expressed small RNA in hepatocellular carcinoma (HCC). This tRNA-derived small RNA (tsRNA) promotes HCC cell proliferation and migration, suggesting an oncogenic role in liver cancer.
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- Hepatocellular carcinoma (HCC) presents a significant global health challenge due to high morbidity and mortality.
- tRNA-derived small RNAs (tsRNAs) are emerging as critical regulators in various cancers, with potential as therapeutic targets.
- The specific role of tsRNAs in the pathogenesis of HCC remains largely unexplored.
Purpose of the Study:
- To investigate the biological significance and oncogenic potential of tsRNAs in hepatocellular carcinoma.
- To identify specific tsRNAs differentially expressed in HCC tissues and their correlation with clinicopathological features.
- To elucidate the functional impact of a key tsRNA on HCC cell proliferation and migration.
Main Methods:
- High-throughput sequencing to screen differentially expressed tsRNAs in HCC versus adjacent normal tissues.
- Agarose gel electrophoresis, nuclear-cytoplasmic separation, and fluorescence in situ hybridization for tsRNA characterization.
- In vitro assays including CCK-8, colony formation, EdU staining, and Transwell assays to assess proliferation and migration.
Main Results:
- tRF-39-8HM2OSRNLNKSEKH9 was significantly upregulated in HCC tissues compared to normal adjacent tissues.
- Elevated tRF-39-8HM2OSRNLNKSEKH9 expression correlated positively with larger tumor size in HCC patients.
- Overexpression of tRF-39-8HM2OSRNLNKSEKH9 enhanced HCC cell proliferation and accelerated cell migration.
Conclusions:
- tRF-39-8HM2OSRNLNKSEKH9 is highly expressed in HCC cells, serum, and tissues.
- This tsRNA demonstrates an oncogenic role in HCC by promoting cell proliferation and migration.
- tRF-39-8HM2OSRNLNKSEKH9 represents a potential diagnostic biomarker and therapeutic target for hepatocellular carcinoma.
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