Evidence map›Paper›PMID 40789668›Full record

ArticleJournal of biomedical research2026

piR-61298 promotes colorectal cancer progression through destabilizing p53 by interacting with USP10.

Shenya Xu, Zhutao Ding, Shuai Ben, Chen Li, Silu Chen, Lingyan Zhao, Shuwei Li, Dongying Gu

Abstract read
In one paragraph

Article in Journal of biomedical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Shenya XuDepartment of Oncology, Nanjing First Hospital, Nanjing Medical University, Nanjing, Jiangsu 210006, China.
Zhutao DingDepartment of Oncology, Nanjing First Hospital, Nanjing Medical University, Nanjing, Jiangsu 210006, China.
Shuai BenDepartment of Genetic Toxicology, the Key Laboratory of Modern Toxicology of Ministry of Education, Key Laboratory of Public Health Safety and Emergency Prevention and Control Technology of Higher Education Institutions in Jiangsu Province, Center for Global Health, School of Public Health, Nanjing Medical University, Nanjing, Jiangsu 211166, China.
Chen LiDepartment of Oncology, Nanjing First Hospital, Nanjing Medical University, Nanjing, Jiangsu 210006, China.
Silu ChenDepartment of Oncology, Nanjing First Hospital, Nanjing Medical University, Nanjing, Jiangsu 210006, China.
Lingyan ZhaoDepartment of Oncology, Nanjing First Hospital, Nanjing Medical University, Nanjing, Jiangsu 210006, China.
Shuwei LiDepartment of Genetic Toxicology, the Key Laboratory of Modern Toxicology of Ministry of Education, Key Laboratory of Public Health Safety and Emergency Prevention and Control Technology of Higher Education Institutions in Jiangsu Province, Center for Global Health, School of Public Health, Nanjing Medical University, Nanjing, Jiangsu 211166, China.
Dongying GuDepartment of Oncology, Nanjing First Hospital, Nanjing Medical University, Nanjing, Jiangsu 210006, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PIWI-interacting RNAs (piRNAs) are a class of noncoding RNAs primarily found in germ cells. While piRNAs are known to be involved in various cancers, their specific roles in colorectal cancer (CRC) remain unclear. To elucidate the role of piRNAs in CRC, we first analyzed their expression characteristics by sequencing 10 pairs of tumor and adjacent normal tissues. Subsequently, differentially expressed piRNAs were identified through a two-stage reverse transcription-quantitative PCR (RT-qPCR) validation using 20 and 114 pairs of samples. Subcellular localization was assessed through nucleoplasmic separation and immunofluorescence staining assays. RNA pull-down mass spectrometry was employed to identify piRNA-interacting proteins. We identified piR-61298 as a piRNA significantly upregulated in CRC. Functional assays showed that piR-61298 promoted cell proliferation and migration, inhibited apoptosis, and promoted tumor growth. Mechanistically, piR-61298 bound to ubiquitin-specific peptidase 10 (USP10) in the cytoplasm, impairing its deubiquitinating activity toward p53, thereby leading to p53 ubiquitination and degradation. These findings suggest that piR-61298 plays a critical role in CRC progression by disrupting the USP10-p53 axis. Collectively, the current study highlights piR-61298 as a potential therapeutic target, offering a novel approach for CRC treatment by targeting piRNA-mediated regulation.

Indexed as

colorectal cancerdeubiquitinationp53piRNAUSP10

Identifiers

PMID40789668
PMCPMC13231362

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.