# Antiviral Shrimp lncRNA06 Possesses Anti-Tumor Activity by Inducing Apoptosis of Human Gastric Cancer Stem Cells in a Cross-Species Manner

**Authors:** Ahmad Khan, Anas Mohammed, Xiaobo Zhang

PMC · DOI: 10.3390/md22050221 · Marine Drugs · 2024-05-15

## TL;DR

A shrimp lncRNA with antiviral properties can reduce human gastric cancer stem cell growth by inducing apoptosis and suppressing stemness.

## Contribution

Discovery that antiviral shrimp lncRNA06 has cross-species anti-tumor activity by targeting human cancer stem cells.

## Key findings

- Shrimp lncRNA06 suppresses human gastric cancer stem cell tumorigenesis via apoptosis induction.
- lncRNA06 sponges miR-17-5p and interacts with ATP5F1B to inhibit cancer stemness.
- In vivo experiments confirm lncRNA06's anti-tumor effects in human gastric cancer models.

## Abstract

Virus infection causes the metabolic disorder of host cells, whereas the metabolic disorder of cells is one of the major causes of tumorigenesis, suggesting that antiviral molecules might possess anti-tumor activities by regulating cell metabolism. As the key regulators of gene expression, long non-coding RNAs (lncRNAs) play vital roles in the regulation of cell metabolism. However, the influence of antiviral lncRNAs on tumorigenesis has not been explored. To address this issue, the antiviral and anti-tumor capacities of shrimp lncRNAs were characterized in this study. The results revealed that shrimp lncRNA06, having antiviral activity in shrimp, could suppress the tumorigenesis of human gastric cancer stem cells (GCSCs) via triggering apoptosis of GCSCs in a cross-species manner. Shrimp lncRNA06 could sponge human miR-17-5p to suppress the stemness of GCSCs via the miR-17-5p-p21 axis. At the same time, shrimp lncRNA06 could bind to ATP synthase subunit beta (ATP5F1B) to enhance the stability of the ATP5F1B protein in GCSCs, thus suppressing the tumorigenesis of GCSCs. The in vivo data demonstrated that shrimp lncRNA06 promoted apoptosis and inhibited the stemness of GCSCs through interactions with ATP5F1B and miR-17-5p, leading to the suppression of the tumorigenesis of GCSCs. Therefore, our findings highlighted that antiviral lncRNAs possessed anti-tumor capacities and that antiviral lncRNAs could be the anti-tumor reservoir for the treatment of human cancers.

## Linked entities

- **Genes:** MIR17 (microRNA 17) [NCBI Gene 406952], CDKN1A (cyclin dependent kinase inhibitor 1A) [NCBI Gene 1026], ATP5F1B (ATP synthase F1 subunit beta) [NCBI Gene 506]
- **Proteins:** ATP5F1B (ATP synthase F1 subunit beta)
- **Diseases:** gastric cancer (MONDO:0001056)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** H3P16 (H3 histone pseudogene 16) [NCBI Gene 644914] {aka H3.6, H3F3AP6, p21}, MIR17 (microRNA 17) [NCBI Gene 406952] {aka MIR17-5p, MIR91, MIRN17, MIRN91, hsa-mir-17, miR-17}
- **Diseases:** Gastric Cancer (MESH:D013274), tumorigenesis (MESH:D063646), metabolic disorder (MESH:D008659), Tumor (MESH:D009369), infection (MESH:D007239)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11123040/full.md

## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC11123040/full.md

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Source: https://tomesphere.com/paper/PMC11123040