Evidence map›Paper›PMID 38585725›Full record

ArticlebioRxiv : the preprint server for biology2024

Large-scale RNA-seq mining reveals ciclopirox triggers TDP-43 cryptic exons.

Irika R Sinha, Parker S Sandal, Grace D Burns, Aswathy Peethambaran Mallika, Katherine E Irwin, Anna Lourdes F Cruz, Vania Wang, Josué Llamas Rodríguez, Philip C Wong, Jonathan P Ling

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. 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, 7 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Irika R SinhaDepartment of Neuroscience, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.ORCID 0000-0001-6440-7019
Parker S SandalDepartment of Neuroscience, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.
Grace D BurnsDepartment of Pathology, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.ORCID 0000-0001-8691-779X
Aswathy Peethambaran MallikaDepartment of Pathology, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.ORCID 0000-0003-0303-5156
Katherine E IrwinDepartment of Neuroscience, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.ORCID 0000-0001-8941-4557
Anna Lourdes F CruzDepartment of Neuroscience, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.ORCID 0000-0002-9889-3868
Vania WangDepartment of Oncology, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.ORCID 0000-0002-9428-7019
Josué Llamas RodríguezDepartment of Neuroscience, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.ORCID 0000-0002-5532-7786
Philip C WongDepartment of Neuroscience, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.ORCID 0000-0001-8162-3274
Jonathan P LingDepartment of Pathology, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.ORCID 0000-0003-1927-9729
Johns Hopkins University · US

Funding

Training Program in NeuroscienceT32NS091018 · NINDS · JOHNS HOPKINS UNIVERSITY · PI JAMES J KNIERIM, Daniel Hans O'Connor · 2015 to 2026
$4.1M
TDP-43 Proteinopathy in ALS-FTD: Mechanism, Target Validation and BiomarkerR01NS095969 · NINDS · JOHNS HOPKINS UNIVERSITY · PI PHILIP C WONG · 2016 to 2026
$2.4M
Functional Validation of TDP-43 splicing repression for frontotemporal degenerationUH3NS115608 · NINDS · JOHNS HOPKINS UNIVERSITY · PI WONG, PHILIP C · 2021 to 2022
$2.2M
A diagnostic biomarker for amyotrophic lateral sclerosisU01FD008129 · FDA · JOHNS HOPKINS UNIVERSITY · PI BERRY, JAMES DALE, WONG, PHILIP C · 2023 to 2023
$1.6M
Generation and characterization of a mouse model exhibiting beta-amyloidosis and tauopathy with nuclear depletion of TDP-43R33NS115161 · NINDS · JOHNS HOPKINS UNIVERSITY · PI WONG, PHILIP C · 2022 to 2023
$1.3M
FDA HHS U01 FD008129NINDS NIH HHS R01 NS095969NINDS NIH HHS R33 NS115161NINDS NIH HHS T32 NS091018NINDS NIH HHS UH3 NS115608
6 · The paper itself

Abstract

Nuclear clearance and cytoplasmic aggregation of TDP-43 in neurons, initially identified in ALS-FTD, are hallmark pathological features observed across a spectrum of neurodegenerative diseases. We previously found that TDP-43 loss-of-function leads to the transcriptome-wide inclusion of deleterious cryptic exons in brains and biofluids post-mortem as well as during the presymptomatic stage of ALS-FTD, but upstream mechanisms that lead to TDP-43 dysregulation remain unclear. Here, we developed a web-based resource (SnapMine) to determine the levels of TDP-43 cryptic exon inclusion across hundreds of thousands of publicly available RNA sequencing datasets. We established cryptic exon inclusion across a variety of human cells and tissues to provide ground truth references for future studies on TDP-43 dysregulation. We then explored studies that were entirely unrelated to TDP-43 or neurodegeneration and found that ciclopirox olamine (CPX), an FDA-approved antifungal, can trigger the inclusion of TDP-43-associated cryptic exons in a variety of mouse and human primary cells. CPX induction of cryptic exon occurs via heavy metal toxicity and oxidative stress, suggesting that similar vulnerabilities could play a role in neurodegeneration. Our work demonstrates how diverse datasets can be linked through common biological features and underscores that public archives of sequencing data represent a vastly underutilized resource with tremendous potential for uncovering novel insights into complex biological mechanisms and diseases.

Identifiers

PMID38585725
PMCPMC10996699
OpenAlexW4393339243

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.