Evidence map›Paper›PMID 40098362›Full record

ArticleACS chemical neuroscience2025

Selection of DNA Aptamers That Promote Neurite Outgrowth in Human iPSC-Derived Sensory Neuron Organoid Cultures.

Brandon Wilbanks, Jenelle Rolli, Keenan Pearson, Sybil C L Hrstka, Ronald F Hrstka, Arthur E Warrington, Nathan P Staff, L James Maher

Abstract read
In one paragraph

Article in ACS chemical neuroscience, 2025. 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. Methods for cell- and tissue-specific DNA aptamer selection.Molecular therapy. Methods & clinical development · 2025
    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.

Brandon WilbanksDepartment of Biochemistry and Molecular Biology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota 55905, United States.
Jenelle RolliDepartment of Biochemistry and Molecular Biology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota 55905, United States.
Keenan PearsonDepartment of Biochemistry and Molecular Biology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota 55905, United States.
Sybil C L HrstkaDepartment of Neurology, Mayo Clinic, Rochester, Minnesota 55905, United States.
Ronald F HrstkaDepartment of Neurology, Mayo Clinic, Rochester, Minnesota 55905, United States.
Arthur E WarringtonDepartment of Neurologic Surgery, Mayo Clinic, Rochester, Minnesota 55905, United States.
Nathan P StaffDepartment of Neurology, Mayo Clinic, Rochester, Minnesota 55905, United States.
L James MaherDepartment of Biochemistry and Molecular Biology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota 55905, United States.ORCID 0000-0002-5043-6422

Funding

Investigating the role of MAP2 in chemotherapy-induced peripheral neurotoxicityR01CA275870 · NCI · MAYO CLINIC ROCHESTER · PI Nathan P Staff · 2023 to 2026
$2.4M
Fundamental and applied studies of nucleic acidsR35GM143949 · NIGMS · MAYO CLINIC ROCHESTER · PI LOUIS JAMES MAHER · 2022 to 2026
$1.9M
NCI NIH HHS R01 CA275870NIGMS NIH HHS R35 GM143949
6 · The paper itself

Abstract

Sensory neurons in the dorsal root ganglia transmit sensory signals from the periphery to the central nervous system. Induced pluripotent stem cell derived models of sensory neurons and dorsal root ganglia are among the most advanced available tools for the study of sensory neuron activity and development in human genetic backgrounds. However, few available reagents modify sensory neuron growth with disease or other model-relevant outcomes. Small molecules, peptides, or oligonucleotides that predictably alter sensory neuron behavior in these contexts would be valuable tools with potentially wide-ranging application. Here we describe the selection and characterization of DNA aptamers that specifically interact with human sensory neurons. Several selected aptamers increase neurite outgrowth from sensory neuron organoid cultures after single-dose treatments.

Indexed as

Aptamers, NucleotideInduced Pluripotent Stem CellsNeuritesNeuronal OutgrowthOrganoidsSensory Receptor CellsCells, CulturedGanglia, SpinalHumansAptamers, NucleotideDNA aptamerneurite outgrowthneuron organoid culture

Identifiers

PMID40098362
PMCPMC11969424

What OpenQuestion holds

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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.