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MP75-13 IN-VIVO INHIBITION OF MIR-202-5P RESULTS IN SPERMATOGENIC KNOCKDOWN THROUGH TARGETING EPIDERMAL GROWTH FACTOR PATHWAYS & CELL CYCLE REGULATION

2019· article· en· W2941513444 on OpenAlexaboutno aff
Ryan Flannigan, Russell Hayden, Anna Mielnik, Alex Bolyakov, Peter N. Schlegel, Darius A. Paduch

Bibliographic record

VenueThe Journal of Urology · 2019
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicRenal and related cancers
Canadian institutionsnot available
Fundersnot available
KeywordsGene knockdownMedicineIn vivoEpidermal growth factorCell biologyCell growthCancer researchInternal medicineApoptosisGeneticsBiology

Abstract

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You have accessJournal of UrologyInfertility: Basic Research & Pathophysiology (MP75)1 Apr 2019MP75-13 IN-VIVO INHIBITION OF MIR-202-5P RESULTS IN SPERMATOGENIC KNOCKDOWN THROUGH TARGETING EPIDERMAL GROWTH FACTOR PATHWAYS & CELL CYCLE REGULATION Ryan Flannigan*, Russell Hayden, Anna Mielnik, Alex Bolyakov, Peter Schlegel, and Darius Paduch Ryan Flannigan*Ryan Flannigan* More articles by this author , Russell HaydenRussell Hayden More articles by this author , Anna MielnikAnna Mielnik More articles by this author , Alex BolyakovAlex Bolyakov More articles by this author , Peter SchlegelPeter Schlegel More articles by this author , and Darius PaduchDarius Paduch More articles by this author View All Author Informationhttps://doi.org/10.1097/01.JU.0000557252.54021.e0AboutPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareFacebookLinked InTwitterEmail Abstract INTRODUCTION AND OBJECTIVES: Our group has previously demonstrated that men with Sertoli Cell Only Syndrome (SCO) demonstrate a 17x downregulation of miR-202-5p compared to testis biopsies from normal controls. We subsequently demonstrated that using an inducible model of SCO in mice does not deplete miR-202-5p levels. In this study, we sought to computationally evaluate mRNA targets for miR-202-5p, test for miR-202-5p to 3UTR interactions, and evaluate the impact of in vivo delivery of a miR-202-5p inhibitor on spermatogenesis. METHODS: Computationally predicted mRNA targets of miR-202-5p were created using RNAseq and miRNAseq biological data from 44 testis biopsies. A custom multi-parametric, multi-dimensional association of vectors was used to capture both linear and non-linear algorithms via neural network machine learning. To validate miR-202-5p interactions with the 3UTR of CHEK1 gene, a luciferase reporter assay was used. These reporter plasmids were transfected and later transduced in Human Embryonal Kidney (HEK293) cells prior to measuring luciferase activity in the presence of miR-202-5p. To test the in-vivo impact, 50nM FITC-labelled miR-202-5p inhibitor was injected into murine efferent ducts along with a scrambled control miRNA on the contralateral side. Testes were subsequently evaluated via histology and immunofluorescence. RESULTS: MiR-202-5p was found to be heavily implicated in epidermal growth factor (EGF) pathway regulation and cell cycle control. The computationally derived results were validated in vitro with using miRNA-3UTR luciferase reporters where miR-202-5p reduced the luciferase activity of cells transduced with CHEK1 3UTRs but not when the 3UTR was designed with a mutated seed region. We further confirmed the critical role miR-202-5p exerts during spermatogenesis by observing a knockdown of spermatogenesis in murine testis tubules in the presence of a miR-202-5p inhibitor, and maintenance of spermatogenesis in the presence of a scrambled control miRNA. CONCLUSIONS: In follow-up to our previous studies investigating the role of miR-202-5p, we demonstrated that miR-202-5p is largely implicated in EGF pathway regulation in Sertoli cells maintaining an end-differentiated state. Furthermore, we demonstrated that miR-202-5p is critical to spermatogenesis as in vivo inhibition results in spermatogenic knockdown and SCO histopathology. Further research is prudent to determine the role of miR-202-5p therapy to potentially restore spermatogenesis in men with non-obstructive azoospermia. Source of Funding: This work was supported by: P50 HD076210, U1 1U01HD074542-01, Frederick J. and Theresa Dow Wallace Fund of the New York Community Trust, the Mr. Robert S. Dow Foundation, Irena and Howard Laks Foundation; Urology Care Foundation Research Scholar Award Program and AUA New York Section E. Darracott Vaughan MD, Research Scholar Award. Vancouver, Canada; New York, NY© 2019 by American Urological Association Education and Research, Inc.FiguresReferencesRelatedDetails Volume 201Issue Supplement 4April 2019Page: e1087-e1087 Advertisement Copyright & Permissions© 2019 by American Urological Association Education and Research, Inc.MetricsAuthor Information Ryan Flannigan* More articles by this author Russell Hayden More articles by this author Anna Mielnik More articles by this author Alex Bolyakov More articles by this author Peter Schlegel More articles by this author Darius Paduch More articles by this author Expand All Advertisement PDF downloadLoading ...

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.021
Threshold uncertainty score0.070

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.000
Science and technology studies0.0000.000
Scholarly communication0.0010.000
Open science0.0000.000
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0210.004

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.009
GPT teacher head0.218
Teacher spread0.210 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2019
Admission routes1
Has abstractyes

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