Evidence map›Paper›PMID 36547457›Full record

ReviewJournal of cardiovascular development and disease2022

Molecular Mechanism Underlying Role of the XBP1s in Cardiovascular Diseases.

Shu Liu, Hong Ding, Yongnan Li, Xiaowei Zhang

Abstract readReview
In one paragraph

Review in Journal of cardiovascular development and disease, 2022. 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
–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

7 citing papers in PubMed.

  1. ATF3 Deficiency Exacerbates Ageing-Induced Atherosclerosis and Clinical Intervention Strategy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
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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

4 authors.

Shu LiuDepartment of Cardiology, Lanzhou University Second Hospital, Lanzhou University, Lanzhou 730030, China.
Hong DingDepartment of Cardiology, Lanzhou University Second Hospital, Lanzhou University, Lanzhou 730030, China.
Yongnan LiDepartment of Cardiology, Lanzhou University Second Hospital, Lanzhou University, Lanzhou 730030, China.
Xiaowei ZhangDepartment of Cardiology, Lanzhou University Second Hospital, Lanzhou University, Lanzhou 730030, China.

Funding

Gansu Heart Rehabilitation Engineering Research Center CRQI-C00535Gansu Science and Technology Department Project 20YF3WA016Gansu Youth Science and Technology Fund Program 21JR11RA116National Natural Science Foundation of China NSFC 82060080Project of Lanzhou Science and Technology Bureau 2019-RC36
6 · The paper itself

Abstract

Spliced X-box binding protein-1 (XBP1s) is a protein that belongs to the cAMP-response element-binding (CREB)/activating transcription factor (ATF) b-ZIP family with a basic-region leucine zipper (bZIP). There is mounting evidence to suggest that XBP1s performs a critical function in a range of different cardiovascular diseases (CVDs), indicating that it is necessary to gain a comprehensive knowledge of the processes involved in XBP1s in various disorders to make progress in research and clinical therapy. In this research, we provide a summary of the functions that XBP1s performs in the onset and advancement of CVDs such as atherosclerosis, hypertension, cardiac hypertrophy, and heart failure. Furthermore, we discuss XBP1s as a novel therapeutic target for CVDs.

Indexed as

cardiac hypertrophycardiovascular diseasesheart failurehypertensionspliced X-box binding protein-1

Identifiers

PMID36547457
PMCPMC9782920

What OpenQuestion holds

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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.