Evidence map›Paper›PMID 41410327›Full record

SynthesisBiomedica : revista del Instituto Nacional de Salud2025

Advanced artificial intelligence in piRNA and PIWI-like protein research: A systematic review of recurrent neural networks, long short-term memory, and emerging computational techniques

Jheremy Sebastián Reyes, Jhonathan David Guevara, Laura Tatiana Picón, Iris Lorena Sánchez, Libia Andrea Gaona, María Paula Montoya, Luis Eduardo Pino

Abstract readSystematic Review
In one paragraph

Synthesis in Biomedica : revista del Instituto Nacional de Salud, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Jheremy Sebastián ReyesCancer and Molecular Medicine Research Group - CAMMO, Bogotá, D. C., Colombia.ORCID 0000-0002-7366-0881
Jhonathan David GuevaraCancer and Molecular Medicine Research Group - CAMMO, Bogotá, D. C., Colombia.ORCID 0009-0007-2757-664X
Laura Tatiana PicónCancer and Molecular Medicine Research Group - CAMMO, Bogotá, D. C., Colombia.ORCID 0000-0003-2853-7750
Iris Lorena SánchezCancer and Molecular Medicine Research Group - CAMMO, Bogotá, D. C., Colombia.ORCID 0000-0001-6155-5470
Libia Andrea GaonaCancer and Molecular Medicine Research Group - CAMMO, Bogotá, D. C., Colombia.ORCID 0009-0002-7367-4666
María Paula MontoyaCancer and Molecular Medicine Research Group - CAMMO, Bogotá, D. C., Colombia.ORCID 0000-0002-6970-7704
Luis Eduardo PinoCancer and Molecular Medicine Research Group - CAMMO, Bogotá, D. C., Colombia.ORCID 0000-0003-4475-7470

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPIWI-interacting RNAs are small and non-coding RNAs involved in gene regulation and transposable element repression, emerging as critical biomarkers and therapeutic targets in oncology. Advances in artificial intelligence, such as recurrent neural networks, long short-term memory networks, and graph convolutional networks, offer significant improvements in PIWI-interacting RNA detection.

objectivesTo evaluate the performance of artificial intelligence models, including recurrent neural networks, long short-term memory, and graph convolutional networks, in detecting PIWI-interacting RNAs and assessing their implications for cancer diagnostics and prognosis. MATERIALS AND

methodsA systematic review of 24 studies was conducted across PubMed, ScienceDirect, Scopus, and Web of Science, focusing on artificial intelligence-based approaches for PIWI-interacting RNA detection. Inclusion criteria were original articles published in English or Spanish using artificial intelligence models in clinical or experimental settings. Performance metrics such as accuracy, sensitivity, and specificity were analyzed.

resultsLong short-term memory models achieved the highest overall accuracy (92.3%), followed by graph convolutional networks (91.4%), support vector machines (88%), and recurrent neural networks (85.7%). Sensitivity and specificity were also highest in long short-term memory (94% and 91%, respectively). Graph convolutional networks showed superior performance in identifying PIWI-interacting RNA-disease associations with complex datasets. Support vector machine models were effective in smaller datasets but exhibited scalability limitations.

conclusionArtificial intelligence models, especially long short-term memory and graph convolutional networks, significantly enhance PIWI-interacting RNA detection, supporting their application in cancer diagnostics and personalized medicine. Future studies should refine these models, address dataset biases, and explore their integration into clinical workflows.

Indexed as

Argonaute ProteinsArtificial IntelligenceNeural Networks, ComputerRNA, Small InterferingComputational BiologyHumansLong Short Term MemoryNeoplasmsPiwi-Interacting RNARecurrent Neural NetworksArgonaute ProteinsPiwi-Interacting RNARNA, Small InterferingArtificial intelligencecomputerlong-termmedical oncologymemoryneoplasms/diagnosisneural networksprognosis

Identifiers

PMID41410327
PMCPMC12904106

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.