Evidence map›Paper›PMID 36712930›Full record

ArticlePNAS nexus2023

Cystic fibrosis rabbits develop spontaneous hepatobiliary lesions and CF-associated liver disease (CFLD)-like phenotypes.

Qingtian Wu, Xiubin Liang, Xia Hou, Zhenfeng Song, Mohamad Bouhamdan, Yining Qiu, Yui Koike, Carthic Rajagopalan, Hong-Guang Wei, Hong Jiang and 7 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PNAS nexus, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Acquired dysfunction of CFTR underlies cystic fibrosis-like disease of the canine gallbladder.American journal of physiology. Gastrointestinal and liver physiology · 2024
    Article
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 2 institutions in 1 country.

Qingtian WuDepartment of Physiology, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Xiubin LiangCenter for Advanced Models for Translational Sciences and Therapeutics, University of Michigan Medical Center, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Xia HouDepartment of Physiology, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Zhenfeng SongCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Mohamad BouhamdanDepartment of Physiology, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Yining QiuCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Yui KoikeCenter for Advanced Models for Translational Sciences and Therapeutics, University of Michigan Medical Center, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Carthic RajagopalanDepartment of Physiology, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Hong-Guang WeiDepartment of Physiology, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Hong JiangDepartment of Physiology, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Gerry HishLaboratory Animal Resources, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Jifeng ZhangCenter for Advanced Models for Translational Sciences and Therapeutics, University of Michigan Medical Center, University of Michigan Medical School, Ann Arbor, MI 48109, USA.ORCID https://orcid.org/0000-0001-5161-4705
Y Eugene ChenCenter for Advanced Models for Translational Sciences and Therapeutics, University of Michigan Medical Center, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Jian-Ping JinDepartment of Physiology, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Jie XuCenter for Advanced Models for Translational Sciences and Therapeutics, University of Michigan Medical Center, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Kezhong ZhangCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201, USA.ORCID https://orcid.org/0000-0002-6062-235X
Fei SunDepartment of Physiology, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Wayne State University · USUniversity of Michigan · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID P OLSON · 2013 to 2026
$24.3M
Regulation of Hepatic Steatosis by an ER Stress-Inducible Transcription Factor CRR01DK090313 · NIDDK · WAYNE STATE UNIVERSITY · PI Kezhong Zhang · 2011 to 2026
$5.0M
Rabbit model for cystic fibrosisR01HL133162 · NHLBI · WAYNE STATE UNIVERSITY · PI JIN, JIAN-PING, XU, JIE · 2016 to 2019
$2.9M
Regulation of Rhythmic m6A RNA Modification by ER‐associated DegradationR01DK126908 · NIDDK · WAYNE STATE UNIVERSITY · PI FANG, DEYU, ZHANG, KEZHONG · 2021 to 2024
$2.2M
Simultaneous Targeting of IRE1a in B Cells and Macrophages for Lupus TherapyR01AR066634 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI FANG, DEYU, ZHANG, KEZHONG · 2014 to 2018
$1.7M
Mitochondrial NAD kinase: function and mechanism in metabolismR01DK132065 · NIDDK · WAYNE STATE UNIVERSITY · PI ZHANG, KEZHONG, ZHANG, REN · 2022 to 2025
$1.5M
NHLBI NIH HHS R01 HL133162NIAMS NIH HHS R01 AR066634NIDDK NIH HHS P30 DK020572NIDDK NIH HHS R01 DK090313NIDDK NIH HHS R01 DK126908
6 · The paper itself

Abstract

Cystic fibrosis (CF) is an autosomal recessive genetic disease affecting multiple organs. Approximately 30% CF patients develop CF-related liver disease (CFLD), which is the third most common cause of morbidity and mortality of CF. CFLD is progressive, and many of the severe forms eventually need liver transplantation. The mechanistic studies and therapeutic interventions to CFLD are unfortunately very limited. Utilizing the CRISPR/Cas9 technology, we recently generated CF rabbits by introducing mutations to the rabbit CF transmembrane conductance regulator (CFTR) gene. Here we report the liver phenotypes and mechanistic insights into the liver pathogenesis in these animals. CF rabbits develop spontaneous hepatobiliary lesions and abnormal biliary secretion accompanied with altered bile acid profiles. They exhibit nonalcoholic steatohepatitis (NASH)-like phenotypes, characterized by hepatic inflammation, steatosis, and fibrosis, as well as altered lipid profiles and diminished glycogen storage. Mechanistically, our data reveal that multiple stress-induced metabolic regulators involved in hepatic lipid homeostasis were up-regulated in the livers of CF-rabbits, and that endoplasmic reticulum (ER) stress response mediated through IRE1α-XBP1 axis as well as NF-κB- and JNK-mediated inflammatory responses prevail in CF rabbit livers. These findings show that CF rabbits manifest many CFLD-like phenotypes and suggest targeting hepatic ER stress and inflammatory pathways for potential CFLD treatment.

Indexed as

CF rabbitsCF related liver diseasecystic fibrosis

Identifiers

PMID36712930
PMCPMC9832953
OpenAlexW4312155096

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.