Evidence map›Paper›PMID 42239135›Full record

ArticlebioRxiv : the preprint server for biology2026

Transcript architecture predetermines m6A remodeling and sensory neuron vulnerability in chemotherapy-induced peripheral neuropathy.

Md Mamunul Haque, Ohannes K Melemedjian

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. 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

2 authors.

Md Mamunul HaqueDept. of Neural and Pain Sciences, University of Maryland School of Dentistry, Baltimore, Maryland, USA.
Ohannes K MelemedjianDept. of Neural and Pain Sciences, University of Maryland School of Dentistry, Baltimore, Maryland, USA.ORCID 0000-0002-7057-9180

Funding

Identification of novel targets for the treatment of chemotherapy-induced painful peripheral neuropathyR01CA249939 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI MELEMEDJIAN, OHANNES KEVORK · 2020 to 2024
$1.9M
NCI NIH HHS R01 CA249939
6 · The paper itself

Abstract

Whether individual transcripts carry intrinsic features that predetermine their response to perturbations is unknown. Here we used nanopore direct RNA sequencing of male mouse dorsal root ganglia (DRG) to simultaneously profile N6-methyladenosine (m6A) modifications, poly(A) tail dynamics, and full-length isoform identity from mice treated with bortezomib, a proteasome inhibitor that causes painful peripheral neuropathy. Machine learning revealed that transcript-intrinsic features predetermine the magnitude of perturbation-induced m6A loss (R

Identifiers

PMID42239135
PMCPMC13228407

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.