piRNA28846 has the potential to be a novel RNA nucleic acid drug for ovarian cancer

Conventional targeted therapies primarily rely on small molecules and proteins. However, they often struggle to enter specific protein conformations, which limits their therapeutic effectiveness. In contrast, RNA therapy is emerging as a more precise and effective targeting strategy. Through differential analysis comparing Pandora-Seq data with clinical samples, we discovered that the small RNA piR-28846 naturally, occurring in human body, exhibited low expression levels in ovarian cancer tissues. Experimental results indicate that piR-28846 inhibits the growth of ovarian cancer cells. Additionally, piR-28846 demonstrated significant therapeutic effects in xenograft models and ovarian cancer-like organoids. Further studies revealed that piR-28846 binds to NSUN2 and down-regulates it, which in turn affects the stability of KPNA2 mRNA. Notably, KPNA2 negatively regulates NSUN2 expression and localization. Given its inhibitory effects observed in vivo, in vitro, and in the ovarian cancer organoid model, we believe piR-28846 has strong potential as a small nucleic acid therapy of ovarian cancer.

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Publication Details

Journal
npj Precision Oncology
Published
2025-03-08
DOI
https://doi.org/10.1038/s41698-025-00840-w
Citations
2
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
1.61

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article

piRNA28846 has the potential to be a novel RNA nucleic acid drug for ovarian cancer

Qinghua Wu, Yang Zhao, Yang Han, Yongpeng Wang et al.
2 citations
npj Precision Oncology
RNA modifications and cancer
1.61
article

piRNA28846 has the potential to be a novel RNA nucleic acid drug for ovarian cancer

Qinghua Wu, Yang Zhao, Yang Han, Yongpeng Wang, Qian-hui Li, Honglei Qin, Shuo Chen, Xi Chen, Jianqi Li, Yuping Du, Xue Guan, Xiujie Sheng
article en
2 citations

Abstract

Conventional targeted therapies primarily rely on small molecules and proteins. However, they often struggle to enter specific protein conformations, which limits their therapeutic effectiveness. In contrast, RNA therapy is emerging as a more precise and effective targeting strategy. Through differential analysis comparing Pandora-Seq data with clinical samples, we discovered that the small RNA piR-28846 naturally, occurring in human body, exhibited low expression levels in ovarian cancer tissues. Experimental results indicate that piR-28846 inhibits the growth of ovarian cancer cells. Additionally, piR-28846 demonstrated significant therapeutic effects in xenograft models and ovarian cancer-like organoids. Further studies revealed that piR-28846 binds to NSUN2 and down-regulates it, which in turn affects the stability of KPNA2 mRNA. Notably, KPNA2 negatively regulates NSUN2 expression and localization. Given its inhibitory effects observed in vivo, in vitro, and in the ovarian cancer organoid model, we believe piR-28846 has strong potential as a small nucleic acid therapy of ovarian cancer.

npj Precision OncologyVol. 9(1)
Third Affiliated Hospital of Guangzhou Medical University (CN), Liaoning Cancer Hospital & Institute (CN), China Medical University (CN), Guangzhou Medical University (CN)
National Natural Science Foundation of China, Project for Key Medicine Discipline Construction of Guangzhou Municipality, Guangzhou Science and Technology Program key projects
Zero hunger
Openalex Percentile: Top 19%
RNA modifications and cancer
1.61
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