Evidence map›Paper›PMID 36214222›Full record

ArticleJCI insight2022

Long noncoding RNA uc.230/CUG-binding protein 1 axis sustains intestinal epithelial homeostasis and response to tissue injury.

Ting-Xi Yu, Sudhakar Kalakonda, Xiangzheng Liu, Naomi Han, Hee K Chung, Lan Xiao, Jaladanki N Rao, Tong-Chuan He, Jean-Pierre Raufman, Jian-Ying Wang

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Long Noncoding RNANon-coding RNA · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Polyamines regulate mitochondrial metabolism essential for intestinal epithelial renewal and wound healing.American journal of physiology. Gastrointestinal and liver physiology · 2025
    Article
  8. Posttranscriptional Regulation of Intestinal Mucosal Growth and Adaptation by Noncoding RNAs in Critical Surgical Disorders.Journal of investigative surgery : the official journal of the Academy of Surgical Research · 2024
    Review
  9. Article
  10. Article
  11. Stabilization ofAmerican journal of physiology. Gastrointestinal and liver physiology · 2023
    Article
  12. Article
  13. Article
  14. Long Noncoding RNAs in the Pathogenesis of Insulin Resistance.International journal of molecular sciences · 2022
    Review
  15. Review
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

10 authors at 3 institutions in 1 country.

Ting-Xi YuCell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Sudhakar KalakondaCell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Xiangzheng LiuCell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Naomi HanCell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Hee K ChungCell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Lan XiaoCell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Jaladanki N RaoCell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Tong-Chuan HeDepartment of Surgery, The University of Chicago Medical Center, Chicago, Illinois, USA.
Jean-Pierre RaufmanBaltimore Veterans Affairs Medical Center, Baltimore, Maryland, USA.
Jian-Ying WangCell Biology Group, Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland, USA.
University of Maryland, Baltimore · USUniversity of Chicago Medical Center · USVeterans Health Administration · US

Funding

Intestinal Mucosal Growth in Health & Surgical DiseasesR01DK057819 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI Jian-Ying Wang · 2000 to 2026
$7.4M
Surgical Studies of Gut PermeabilityR01DK068491 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI Jian-Ying Wang · 2004 to 2026
$7.0M
Mucosal Repair in Gut Surgical DisordersR01DK061972 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI WANG, JIAN-YING · 2002 to 2023
$6.7M
REGULATION OF INTESTINAL EPITHELIAL RESTITUTIONI01BX000332 · VA · BALTIMORE VA MEDICAL CENTER · PI Jian-Ying Wang · 2009 to 2026
–
BLRD Research Career Scientist Award ApplicationIK6BX004213 · VA · BALTIMORE VA MEDICAL CENTER · PI WANG, JIAN-YING · 2018 to 2025
–
SURGICAL STUDIES ON MUCOSAL HOMEOSTASISI01BX000713 · VA · BALTIMORE VA MEDICAL CENTER · PI WANG, JIAN-YING · 2011 to 2024
–
Muscarinic Receptors Regulate Colon Cancer Stem Cell Function and InvasivenessI01BX004890 · VA · BALTIMORE VA MEDICAL CENTER · PI RAUFMAN, JEAN-PIERRE · 2021 to 2024
–
BLRD VA I01 BX000332BLRD VA I01 BX000713BLRD VA I01 BX004890BLRD VA IK6 BX004213NIDDK NIH HHS R01 DK057819NIDDK NIH HHS R01 DK061972NIDDK NIH HHS R01 DK068491
6 · The paper itself

Abstract

Intestinal epithelial integrity is commonly disrupted in patients with critical disorders, but the exact underlying mechanisms are unclear. Long noncoding RNAs transcribed from ultraconserved regions (T-UCRs) control different cell functions and are involved in pathologies. Here, we investigated the role of T-UCRs in intestinal epithelial homeostasis and identified T-UCR uc.230 as a major regulator of epithelial renewal, apoptosis, and barrier function. Compared with controls, intestinal mucosal tissues from patients with ulcerative colitis and from mice with colitis or fasted for 48 hours had increased levels of uc.230. Silencing uc.230 inhibited the growth of intestinal epithelial cells (IECs) and organoids and caused epithelial barrier dysfunction. Silencing uc.230 also increased IEC vulnerability to apoptosis, whereas increasing uc.230 levels protected IECs against cell death. In mice with colitis, reduced uc.230 levels enhanced mucosal inflammatory injury and delayed recovery. Mechanistic studies revealed that uc.230 increased CUG-binding protein 1 (CUGBP1) by acting as a natural decoy RNA for miR-503, which interacts with Cugbp1 mRNA and represses its translation. These findings indicate that uc.230 sustains intestinal mucosal homeostasis by promoting epithelial renewal and barrier function and that it protects IECs against apoptosis by serving as a natural sponge for miR-503, thereby preserving CUGBP1 expression.

Indexed as

CELF1 ProteinColitisHomeostasisIntestinal MucosaRNA, Long NoncodingWound HealingAnimalsApoptosisMiceMicroRNAsRNA, MessengerWounds and InjuriesCELF1 ProteinCELF1 protein, mouseMicroRNAsMirn503 microRNA, mouseRNA, Long NoncodingRNA, MessengerGastroenterologyInflammatory bowel diseaseSurgery

Identifiers

PMID36214222
PMCPMC9675575
OpenAlexW4303926914

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.