Evidence map›Paper›PMID 28097825›Full record

ReviewJournal of cellular and molecular medicine2017

Signalling pathways involved in hypoxia-induced renal fibrosis.

Minna Liu, Xiaoxuan Ning, Rong Li, Zhen Yang, Xiaoxia Yang, Shiren Sun, Qi Qian

Open access · goldAbstract readReview
In one paragraph

Review in Journal of cellular and molecular medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 125 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
125citing papers in PubMed, 1 pooled it
6.6field-weighted citation impact, top 2% 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

125 citing papers in PubMed, 1 synthesis or guideline pooled it, 211 citations in OpenAlex.

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65 more citing papers are in PubMed but not listed here.

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 at 3 institutions in 2 countries.

Minna LiuDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Xiaoxuan NingDepartment of Geriatrics, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Rong LiDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Zhen YangDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Xiaoxia YangDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Shiren SunDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Qi QianDepartment of Medicine, Division of Nephrology and hypertension, Mayo Clinic College of Medicine, Mayo Graduate School, Rochester, MN, USA.
Air Force Medical University · CNXijing Hospital · CNMayo Clinic in Arizona · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal fibrosis is the common pathological hallmark of progressive chronic kidney disease (CKD) with diverse aetiologies. Recent researches have highlighted the critical role of hypoxia during the development of renal fibrosis as a final common pathway in end-stage kidney disease (ESKD), which joints the scientist's attention recently to exploit the molecular mechanism underlying hypoxia-induced renal fibrogenesis. The scaring formation is a multilayered cellular response and involves the regulation of multiple hypoxia-inducible signalling pathways and complex interactive networks. Therefore, this review will focus on the signalling pathways involved in hypoxia-induced pathogenesis of interstitial fibrosis, including pathways mediated by HIF, TGF-β, Notch, PKC/ERK, PI3K/Akt, NF-κB, Ang II/ROS and microRNAs. Roles of molecules such as IL-6, IL-18, KIM-1 and ADO are also reviewed. A comprehensive understanding of the roles that these hypoxia-responsive signalling pathways and molecules play in the context of renal fibrosis will provide a foundation towards revealing the underlying mechanisms of progression of CKD and identifying novel therapeutic targets. In the future, promising new effective therapy against hypoxic effects may be successfully translated into the clinic to alleviate renal fibrosis and inhibit the progression of CKD.

Indexed as

Cell HypoxiaFibrosisHumansKidneyKidney Failure, ChronicMicroRNAsNF-kappa BReceptors, NotchSignal TransductionTransforming Growth Factor betaMicroRNAsNF-kappa BReceptors, NotchTransforming Growth Factor betahypoxiarenal fibrosisSignalling pathways

Identifiers

PMID28097825
PMCPMC5487923
OpenAlexW2579804224

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.