Evidence map›Paper›PMID 34445377›Full record

ReviewInternational journal of molecular sciences2021

Therapeutic Approaches Targeting Proteostasis in Kidney Disease and Fibrosis.

Jia-Huang Chen, Chia-Hsien Wu, Chih-Kang Chiang

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
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

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
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  8. Markers and mechanisms of death inFrontiers in aging · 2023
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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

3 authors at 1 institution in 2 countries.

Jia-Huang ChenGraduate Institute of Toxicology, College of Medicine, National Taiwan University, Taipei 100233, Taiwan.
Chia-Hsien WuGraduate Institute of Toxicology, College of Medicine, National Taiwan University, Taipei 100233, Taiwan.ORCID 0000-0002-2487-2984
Chih-Kang ChiangGraduate Institute of Toxicology, College of Medicine, National Taiwan University, Taipei 100233, Taiwan.ORCID 0000-0001-9021-4616
National Taiwan University · TW

Funding

Ministry of Science and Technology, Taiwan MOST-104-2314-B-002-126-MY3Ministry of Science and Technology, Taiwan MOST-107-2314-B-002-027-MY3Ministry of Science and Technology, Taiwan MOST- 110-2314-B-002 -130National Taiwan University Hospital NTUH-110-S5063
6 · The paper itself

Abstract

Pathological insults usually disturb the folding capacity of cellular proteins and lead to the accumulation of misfolded proteins in the endoplasmic reticulum (ER), which leads to so-called "ER stress". Increasing evidence indicates that ER stress acts as a trigger factor for the development and progression of many kidney diseases. The unfolded protein responses (UPRs), a set of molecular signals that resume proteostasis under ER stress, are thought to restore the adaptive process in chronic kidney disease (CKD) and renal fibrosis. Furthermore, the idea of targeting UPRs for CKD treatment has been well discussed in the past decade. This review summarizes the up-to-date literature regarding studies on the relationship between the UPRs, systemic fibrosis, and renal diseases. We also address the potential therapeutic possibilities of renal diseases based on the modulation of UPRs and ER proteostasis. Finally, we list some of the current UPR modulators and their therapeutic potentials.

Indexed as

Endoplasmic ReticulumEndoplasmic Reticulum StressFibrosisHumansMolecular Targeted TherapyProteostasisRenal Insufficiency, ChronicSignal TransductionSmall Molecule LibrariesUnfolded Protein ResponseSmall Molecule Librariesendoplasmic reticulum stressfibrosiskidneyproteostasisunfolded protein responses

Identifiers

PMID34445377
PMCPMC8395452
OpenAlexW3187652427

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.