Evidence map›Paper›PMID 41278873›Full record

ArticlebioRxiv : the preprint server for biology2025

Detection of probable neuronal gene expression changes in skin biopsies from patients with paclitaxel-induced peripheral neuropathy.

Andi Wangzhou, Surendra Dasari, Diana Tavares-Ferreira, Sybil Hrstka, Sandra Rieger, Nathan P Staff, Theodore J Price

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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.

Andi WangzhouDepartment of Neuroscience, Center for Advanced Pain Studies, The University of Texas at Dallas, Richardson TX, USA.
Surendra DasariMayo Clinic, Department of Quantitative Health Sciences, Rochester, MN, USA.
Diana Tavares-FerreiraDepartment of Neuroscience, Center for Advanced Pain Studies, The University of Texas at Dallas, Richardson TX, USA.ORCID 0000-0003-0986-3630
Sybil HrstkaMayo Clinic, Department of Neurology, Rochester, MN, USA.
Sandra RiegerDepartment of Biology, University of Miami, Coral Gables, FL 33146, USA.ORCID 0000-0002-9059-1670
Nathan P StaffMayo Clinic, Department of Neurology, Rochester, MN, USA.
Theodore J PriceDepartment of Neuroscience, Center for Advanced Pain Studies, The University of Texas at Dallas, Richardson TX, USA.ORCID 0000-0002-6971-6221

Funding

Mechanistic underpinnings of chronic low back painU19NS130608 · NINDS · UNIVERSITY OF TEXAS DALLAS · PI Diana Tavares Ferreira · 2022 to 2026
$13.6M
Investigating the role of MAP2 in chemotherapy-induced peripheral neurotoxicityR01CA275870 · NCI · MAYO CLINIC ROCHESTER · PI Nathan P Staff · 2023 to 2026
$2.4M
(PQ 9) Dysregulation of epidermal MMP-13 as cause of paclitaxel-induced peripheral neuropathyR01CA215973 · NCI · UNIVERSITY OF MIAMI CORAL GABLES · PI RIEGER, SANDRA · 2017 to 2021
$1.7M
NCI NIH HHS R01 CA215973NCI NIH HHS R01 CA275870NINDS NIH HHS U19 NS130608
6 · The paper itself

Abstract

Our inability to obtain nerve samples from the vast majority of neuropathic pain patients impedes our ability to understand the disease, creates challenges in understanding mechanisms in specific patient populations, and limits our ability to make treatment decisions based on quantifiable molecular data. Fields like oncology have overcome these problems to take advantage of the insight that sequencing offers for understanding mechanisms of disease and have leveraged these molecular insights to dramatically change the treatment landscape in the past decade. Here we tested the hypothesis that skin biopsies could be used to gain insight into neuronal transcriptomic changes in patients with paclitaxel-induced peripheral neuropathy (PIPN). Our analysis reveals that hundreds of differentially expressed genes (DEGs) found through bulk RNA sequencing in these skin biopsies are likely contributed by dorsal root ganglion (DRG) neuronal axons and/or terminals. Up-regulated genes were representative of broad class of nociceptors whereas down-regulated genes were associated with putative injured DRG neurons expressing the

Identifiers

PMID41278873
PMCPMC12632969

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.