Evidence map›Paper›PMID 28536261›Full record

ArticleThe Journal of biological chemistry2017

The let-7/Lin28 axis regulates activation of hepatic stellate cells in alcoholic liver injury.

Kelly McDaniel, Li Huang, Keisaku Sato, Nan Wu, Tami Annable, Tianhao Zhou, Sugeily Ramos-Lorenzo, Ying Wan, Qiaobing Huang, Heather Francis and 4 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

45 citing papers in PubMed, 75 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Non-coding RNAs in alcohol-associated liver disease.Liver research (Beijing, China) · 2025
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Reviewing the Regulators of COL1A1.International journal of molecular sciences · 2023
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Drug response biomarkers of Pien Tze Huang treatment for hepatic fibrosis induced by carbon tetrachloride.Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan · 2022
    Article
  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

14 authors at 7 institutions in 2 countries.

Kelly McDanielFrom the Division of Research, Central Texas Veterans Health Care System, Temple, Texas 76504.
Li HuangDepartment of Hepatobiliary Surgery, First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, China.
Keisaku SatoDigestive Disease Research Center, Department of Medicine, Baylor Scott & White Digestive Disease Research Center, Texas A&M Health Science Center, and Baylor Scott & White Hospital, Temple, Texas 76504.
Nan WuDigestive Disease Research Center, Department of Medicine, Baylor Scott & White Digestive Disease Research Center, Texas A&M Health Science Center, and Baylor Scott & White Hospital, Temple, Texas 76504.
Tami AnnableResearch Institute, Baylor Scott & White Health, Temple, Texas 76504.
Tianhao ZhouFrom the Division of Research, Central Texas Veterans Health Care System, Temple, Texas 76504.
Sugeily Ramos-LorenzoResearch Institute, Baylor Scott & White Health, Temple, Texas 76504.
Ying WanDigestive Disease Research Center, Department of Medicine, Baylor Scott & White Digestive Disease Research Center, Texas A&M Health Science Center, and Baylor Scott & White Hospital, Temple, Texas 76504.
Qiaobing HuangDepartment of Pathophysiology, Key Laboratory for Shock and Microcirculation Research of Guangdong Province, Southern Medical University, Guangzhou 510515, China, and.
Heather FrancisFrom the Division of Research, Central Texas Veterans Health Care System, Temple, Texas 76504.
Shannon GlaserFrom the Division of Research, Central Texas Veterans Health Care System, Temple, Texas 76504.
Hidekazu TsukamotoSouthern California Research Center for Alcoholic Liver and Pancreatic Diseases (ALPD) and Cirrhosis, Keck School of Medicine of the University of Southern California and Department of Veterans Affairs Greater Los Angeles Healthcare System, Los Angeles, California 90089.
Gianfranco AlpiniFrom the Division of Research, Central Texas Veterans Health Care System, Temple, Texas 76504, galpini@tamu.edu.
Fanyin MengFrom the Division of Research, Central Texas Veterans Health Care System, Temple, Texas 76504, fmeng@tamu.edu.
Texas A&M Health Science Center · USBaylor Scott & White Health · USBaylor Scott & White Medical Center - Temple · USCentral Texas Veterans Health Care System · USSouthern Medical University · CNSun Yat-sen University · CNUniversity of Southern California · US

Funding

The Southernearch Center for ALPD and CirrhosisP50AA011999 · NIAAA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ANNA S. GUKOVSKAYA · 1999 to 2026
$45.8M
USC RESEARCH CENTER FOR LIVER DISEASES: PILOT PROGRAMSP30DK048522 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI KAPLOWITZ, NEIL · 1995 to 2020
$21.8M
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
Epigenetic Regulation of Alcoholic Liver FibrosisU01AA018663 · NIAAA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI KISSELEVA, TATIANA, MANN, DEREK · 2010 to 2019
$3.7M
The Paracrine Regulation of Mast Cells During Biliary/Cholangiocyte Repair and DamageR01DK108959 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI FRANCIS, HEATHER L · 2016 to 2024
$2.5M
Regulation of Bile Duct Growth in Bile Duct Ligated RatsR01DK062975 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ALPINI, GIANFRANCO D, GLASER, SHANNON STROUD · 2005 to 2014
$1.9M
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
The Role of Stem Cell Derived Microvesicles in Cholestatic Liver InjuryR01DK107310 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ALPINI, GIANFRANCO D, GLASER, SHANNON STROUD · 2015 to 2019
$1.7M
Autocrine/Paracrine Regulation of Intrahepatic Bile Duct GrowthI01BX000574 · VA · RLR VA MEDICAL CENTER · PI ALPINI, GIANFRANCO D · 2009 to 2022
–
Role of Mechanosensitive Receptors During Biliary Proliferation and FibrosisI01BX002192 · VA · OLIN TEAGUE VETERANS CENTER · PI GLASER, SHANNON STROUD · 2014 to 2018
–
Molecular Mechanisms of Stellate Cell Activation in Liver FibrosisI01BX001991 · VA · VA GREATER LOS ANGELES HEALTHCARE SYSTEM · PI HIDEKAZU TSUKAMOTO · 2014 to 2026
–
BLRD VA I01 BX000574BLRD VA I01 BX001724BLRD VA I01 BX001991BLRD VA I01 BX002192BLRD VA I01 BX003031NIAAA NIH HHS P50 AA011999NIAAA NIH HHS U01 AA018663NIDDK NIH HHS P30 DK048522NIDDK NIH HHS R01 DK054811NIDDK NIH HHS R01 DK058411NIDDK NIH HHS R01 DK062975NIDDK NIH HHS R01 DK076898NIDDK NIH HHS R01 DK107310NIDDK NIH HHS R01 DK108959
6 · The paper itself

Abstract

The let-7/Lin28 axis is associated with the regulation of key cellular regulatory genes known as microRNAs in various human disorders and cancer development. This study evaluated the role of the let-7/Lin28 axis in regulating a mesenchymal phenotype of hepatic stellate cells in alcoholic liver injury. We identified that ethanol feeding significantly down-regulated several members of the let-7 family in mouse liver, including let-7a and let-7b. Similarly, the treatment of human hepatic stellate cells (HSCs) with lipopolysaccharide (LPS) and transforming growth factor-β (TGF-β) significantly decreased the expressions of let-7a and let-7b. Conversely, overexpression of let-7a and let-7b suppressed the myofibroblastic activation of cultured human HSCs induced by LPS and TGF-β, as evidenced by repressed ACTA2 (α-actin 2), COL1A1 (collagen 1A1), TIMP1 (TIMP metallopeptidase inhibitor 1), and FN1 (fibronectin 1); this supports the notion that HSC activation is controlled by let-7. A combination of bioinformatics, dual-luciferase reporter assay, and Western blot analysis revealed that Lin28B and high-mobility group AT-hook (HMGA2) were the direct targets of let-7a and let-7b. Furthermore, Lin28B deficiency increased the expression of let-7a/let-7b as well as reduced HSC activation and liver fibrosis in mice with alcoholic liver injury. This feedback regulation of let-7 by Lin28B is verified in hepatic stellate cells isolated by laser capture microdissection from the model. The identification of the let-7/Lin28 axis as an important regulator of HSC activation as well as its upstream modulators and down-stream targets will provide insights into the involvement of altered microRNA expression in contributing to the pathogenesis of alcoholic liver fibrosis and novel therapeutic approaches for human alcoholic liver diseases.

Indexed as

Signal TransductionActinsAnimalsCollagen Type ICollagen Type I, alpha 1 ChainDNA-Binding ProteinsHepatic Stellate CellsHumansLipopolysaccharidesLiverLiver Diseases, AlcoholicMiceMicroRNAsRNA-Binding ProteinsTransforming Growth Factor betaACTA2 protein, humanActa2 protein, mouseActinsCollagen Type ICollagen Type I, alpha 1 ChainDNA-Binding ProteinsLin28A protein, humanLIN28B protein, humanLin28b protein, mouseLin-28 protein, mouseLipopolysaccharidesMicroRNAsmirnlet7 microRNA, humanmirnlet7 microRNA, mouseRNA-Binding ProteinsTransforming Growth Factor betaalcoholic liver diseasesfibroblastgene knockouthepatic stellate cell (HSC)HMGA2let-7lin28liver injurymicroRNA (miRNA)

Identifiers

PMID28536261
PMCPMC5500799
OpenAlexW2617506376

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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.