Evidence map›Paper›PMID 32180083›Full record

ReviewMolecular biology reports2020

Decrypting the crosstalk of noncoding RNAs in the progression of IPF.

Yujuan Wang, Han Xiao, Fenglian Zhao, Han Li, Rong Gao, Bingdi Yan, Jin Ren, Junling Yang

Open access · hybridAbstract readReview
PubMed Publisher
In one paragraph

Review in Molecular biology reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Unwinding circular RNA's role in inflammatory pulmonary diseases.Naunyn-Schmiedeberg's archives of pharmacology · 2024
    Review
  5. Review
  6. Article
  7. Article
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

8 authors at 1 institution in 1 country.

Yujuan WangDepartment of Respiratory Medicine, The Second Hospital of Jilin University, Changchun, China.
Han XiaoDepartment of Respiratory Medicine, The Second Hospital of Jilin University, Changchun, China.
Fenglian ZhaoDepartment of Respiratory Medicine, The Second Hospital of Jilin University, Changchun, China.
Han LiDepartment of Respiratory Medicine, The Second Hospital of Jilin University, Changchun, China.
Rong GaoDepartment of Respiratory Medicine, The Second Hospital of Jilin University, Changchun, China.
Bingdi YanDepartment of Respiratory Medicine, The Second Hospital of Jilin University, Changchun, China.
Jin RenDepartment of Respiratory Medicine, The Second Hospital of Jilin University, Changchun, China.
Junling YangDepartment of Respiratory Medicine, The Second Hospital of Jilin University, Changchun, China. junling@jlu.edu.cn.ORCID http://orcid.org/0000-0001-8360-2901
Second Affiliated Hospital of Jilin University · CN

Funding

Department of Science and Technology of Jilin Province (CN) 20190201279JCThe Provincial Special Fund for Industrial Innovation from Jilin Province 2017C058-3
6 · The paper itself

Abstract

Idiopathic pulmonary fibrosis (IPF) is an agnogenic, rare, and lethal disease, with high mortality and poor prognosis and a median survival time as short as 3 to 5 years after diagnosis. No effective therapeutic drugs are still not available not only in clinical practice, but also in preclinical phases. To better and deeper understand pulmonary fibrosis will provide more effective strategies for therapy. Mounting evidence suggests that noncoding RNAs (ncRNAs) and their interactions may contribute to lung fibrosis; however, the mechanisms underlying their roles are largely unknown. In this review, we systematically summarized the recent advances regarding the crucial roles of long non-coding RNAs (lncRNAs), microRNAs (miRNAs), and circular RNAs (circRNAs) and crosstalk among them in the development of IPF. The perspective for related genes was well highlighted. In summary, ncRNA and their interactions play a key regulatory part in the progression of IPF and are bound to provide us with new diagnostic and therapeutic targets.

Indexed as

Disease ProgressionHumansIdiopathic Pulmonary FibrosisMicroRNAsRNA, Long NoncodingRNA, UntranslatedMicroRNAsRNA, Long NoncodingRNA, UntranslatedcircRNAcrosstalkIPFlncRNAmiRNAncRNA

Identifiers

PMID32180083
OpenAlexW3012449349

What OpenQuestion holds

Textmetadata
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.