Evidence map›Paper›PMID 25118289›Full record

ArticleThe Journal of biological chemistry2014

Regulation of the extrinsic apoptotic pathway by microRNA-21 in alcoholic liver injury.

Heather Francis, Kelly McDaniel, Yuyan Han, Xiuping Liu, Lindsey Kennedy, Fuquan Yang, Jennifer McCarra, Tianhao Zhou, Shannon Glaser, Julie Venter and 6 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

57 citing papers in PubMed, 91 citations in OpenAlex.

  1. Article
  2. Article
  3. miRNAs and Alcohol-Related Hepatitis.Current issues in molecular biology · 2025
    Review
  4. Review
  5. Review
  6. Non-coding RNAs in alcohol-associated liver disease.Liver research (Beijing, China) · 2025
    Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Epigenetics of alcohol-related liver diseases.JHEP reports : innovation in hepatology · 2022
    Review
  17. Preparation of Active Peptides fromMolecules (Basel, Switzerland) · 2022
    Article
  18. Noncoding RNAs in apoptosis: identification and function.Turkish journal of biology = Turk biyoloji dergisi · 2022
    Review
  19. Article
  20. 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

16 authors at 6 institutions in 2 countries.

Heather FrancisFrom the Research, Central Texas Veterans Health Care System and the Department of Medicine and Scott & White Digestive Disease Research Center, Texas A&M Health Science Center College of Medicine and Scott & White Hospital, Temple, Texas 76504.
Kelly McDanielFrom the Research, Central Texas Veterans Health Care System and the Department of Medicine and Scott & White Digestive Disease Research Center, Texas A&M Health Science Center College of Medicine and Scott & White Hospital, Temple, Texas 76504.
Yuyan Hanthe Department of Medicine and Scott & White Digestive Disease Research Center, Texas A&M Health Science Center College of Medicine and Scott & White Hospital, Temple, Texas 76504.
Xiuping Liuthe Department of Experimental Therapeutics, Division of Cancer Medicine, University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030.
Lindsey KennedyFrom the Research, Central Texas Veterans Health Care System and the Department of Medicine and Scott & White Digestive Disease Research Center, Texas A&M Health Science Center College of Medicine and Scott & White Hospital, Temple, Texas 76504.
Fuquan Yangthe Department of Hepatobiliary Surgery, Shengjing Hospital, China Medical University, Shenyang 100004, China, and.
Jennifer McCarrathe Department of Medicine and Scott & White Digestive Disease Research Center, Texas A&M Health Science Center College of Medicine and Scott & White Hospital, Temple, Texas 76504.
Tianhao Zhouthe Department of Medicine and Scott & White Digestive Disease Research Center, Texas A&M Health Science Center College of Medicine and Scott & White Hospital, Temple, Texas 76504.
Shannon GlaserFrom the Research, Central Texas Veterans Health Care System and the Department of Medicine and Scott & White Digestive Disease Research Center, Texas A&M Health Science Center College of Medicine and Scott & White Hospital, Temple, Texas 76504.
Julie Venterthe Department of Medicine and Scott & White Digestive Disease Research Center, Texas A&M Health Science Center College of Medicine and Scott & White Hospital, Temple, Texas 76504.
Li Huangthe Department of Hepatobiliary Surgery, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, China.
Phillip Levinethe Department of Medicine and Scott & White Digestive Disease Research Center, Texas A&M Health Science Center College of Medicine and Scott & White Hospital, Temple, Texas 76504.
Jia-Ming Laithe Department of Hepatobiliary Surgery, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, China.
Chang-Gong Liuthe Department of Experimental Therapeutics, Division of Cancer Medicine, University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030.
Gianfranco AlpiniFrom the Research, Central Texas Veterans Health Care System and the Department of Medicine and Scott & White Digestive Disease Research Center, Texas A&M Health Science Center College of Medicine and Scott & White Hospital, Temple, Texas 76504, galpini@tamu.edu.
Fanyin MengFrom the Research, Central Texas Veterans Health Care System and the Department of Medicine and Scott & White Digestive Disease Research Center, Texas A&M Health Science Center College of Medicine and Scott & White Hospital, Temple, Texas 76504, fmeng@tamu.edu.
Texas A&M Health Science Center · USScott & White Memorial Hospital · USCentral Texas Veterans Health Care System · USThe First Affiliated Hospital, Sun Yat-sen University · CNThe University of Texas MD Anderson Cancer Center · USChina Medical University · CN

Funding

The Southernearch Center for ALPD and CirrhosisP50AA011999 · NIAAA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI HIDEKAZU TSUKAMOTO · 1999 to 2026
$45.8M
GROWTH REGULATION OF THE INTRAHEPATIC BILIARY TREER01DK054811 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ALPINI, GIANFRANCO D, GLASER, SHANNON STROUD · 2000 to 2021
$3.8M
Role of Sensory Neuropeptides in the Regulation of Biliary FunctionR01DK076898 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ALPINI, GIANFRANCO D, GLASER, SHANNON STROUD · 2008 to 2016
$1.8M
TOWARD THE OPTIMAL TIMING OF INITIATION OF DIALYSISR01DK058411 · NIDDK · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI CHERTOW, GLENN MATTHEW · 2001 to 2003
$1.8M
RESEARCH TRAINING IN SURGICAL GASTROENTEROLOGYT32DK007698 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MULHOLLAND, MICHAEL W. · 1994 to 2003
$335k
Histamine modulation of biliary proliferation and damageIK2BX001760 · VA · OLIN TEAGUE VETERANS CENTER · PI FRANCIS, HEATHER L · 2013 to 2015
–
Functional characters of non-coding RNAs in alcoholic liver injuryI01BX001724 · VA · RLR VA MEDICAL CENTER · PI MENG, FANYIN · 2012 to 2024
–
BLRD VA I01 BX001724BLRD VA IK2 BX001760NIAAA NIH HHS P50 AA011999NIDDK NIH HHS DK07698NIDDK NIH HHS DK58411NIDDK NIH HHS R01 DK054811NIDDK NIH HHS R01 DK058411NIDDK NIH HHS R01 DK076898NIDDK NIH HHS T32 DK007698
6 · The paper itself

Abstract

IL-6/Stat3 is associated with the regulation of transcription of key cellular regulatory genes (microRNAs) during different types of liver injury. This study evaluated the role of IL-6/Stat3 in regulating miRNA and miR-21 in alcoholic liver disease. By microarray, we identified that ethanol feeding significantly up-regulated 0.8% of known microRNAs in mouse liver compared with controls, including miR-21. Similarly, the treatment of normal human hepatocytes (N-Heps) and hepatic stellate cells (HSCs) with ethanol and IL-6 significantly increased miR-21 expression. Overexpression of miR-21 decreased ethanol-induced apoptosis in both N-Heps and HSCs. The expression level of miR-21 was significantly increased after Stat3 activation in N-Heps and HSCs, in support of the concept that the 5'-promoter region of miR-21 is regulated by Stat3. Using real time PCR, we confirmed that miR-21 activation is associated with ethanol-linked Stat3 binding of the miR-21 promoter. A combination of bioinformatics, PCR array, dual-luciferase reporter assay, and Western blot analysis revealed that Fas ligand (TNF superfamily, member 6) (FASLG) and death receptor 5 (DR5) are the direct targets of miR-21. Furthermore, inhibition of miR-21 by specific Vivo-Morpholino and knock-out of IL-6 in ethanol-treated mice also increased the expression of DR5 and FASLG in vivo during alcoholic liver injury. The identification of miR-21 as an important regulator of hepatic cell survival, transformation, and remodeling in vitro, as well as its upstream modulators and downstream targets, will provide insight into the involvement of altered miRNA expression in contributing to alcoholic liver disease progression and testing novel therapeutic approaches for human alcoholic liver diseases.

Indexed as

ApoptosisAnimalsHepatic Stellate CellsHumansInterleukin-6LiverLiver Diseases, AlcoholicMiceMice, Inbred C57BLMicroRNAsSignal TransductionSTAT3 Transcription FactorUp-RegulationInterleukin-6MicroRNAsMIRN21 microRNA, humanMIRN21 microRNA, mouseSTAT3 Transcription FactorAlcoholAlcoholic Liver DiseasesDR5FASLGInterleukin 6 (IL-6)Liver InjuryMicroRNA (miRNA)STAT3

Identifiers

PMID25118289
PMCPMC4183793
OpenAlexW2063452799

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.