Evidence map›Paper›PMID 39135385›Full record

ReviewClinical and translational medicine2024

HSP47 in human diseases: Navigating pathophysiology, diagnosis and therapy.

Essak S Khan, Tobias Däinghaus

Abstract readReview
In one paragraph

Review in Clinical and translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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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.

Essak S KhanPosttranscriptional Gene Regulation, Cancer Research and Experimental Hemostasis, University Medical Center Mainz (UMCM), Mainz, Germany.ORCID 0000-0001-5691-4854
Tobias DäinghausPosttranscriptional Gene Regulation, Cancer Research and Experimental Hemostasis, University Medical Center Mainz (UMCM), Mainz, Germany.

Funding

DGKL SPMD Grant and University Medical Center Mainz (UMCM)German Research Foundation (DFG) 507581264
6 · The paper itself

Abstract

Heat shock protein 47 (HSP47) is a chaperone protein responsible for regulating collagen maturation and transport, directly impacting collagen synthesis levels. Aberrant HSP47 expression or malfunction has been associated with collagen-related disorders, most notably fibrosis. Recent reports have uncovered new functions of HSP47 in various cellular processes. Hsp47 dysregulation in these alternative roles has been linked to various diseases, such as cancer, autoimmune and neurodegenerative disorders, thereby highlighting its potential as both a diagnostic biomarker and a therapeutic target. In this review, we discuss the pathophysiological roles of HSP47 in human diseases, its potential as a diagnostic tool, clinical screening techniques and its role as a target for therapeutic interventions.

Indexed as

HSP47 Heat-Shock ProteinsHumansNeoplasmsHSP47 Heat-Shock Proteinsbiomarkerheat shock protein 47 (HSP47)human disorderstherapy

Identifiers

PMID39135385
PMCPMC11319607

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.