Evidence map›Paper›PMID 28114741›Full record

ArticleHepatology (Baltimore, Md.)2017

Loss of the transforming growth factor-β effector β2-Spectrin promotes genomic instability.

Jian Chen, Vivek Shukla, Patrizia Farci, Jaclyn Andricovich, Wilma Jogunoori, Lawrence N Kwong, Lior H Katz, Kirti Shetty, Asif Rashid, Xiaoping Su and 18 more

Open access · greenAbstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

26 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
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  7. Impaired reciprocal regulation between SIRT6 and TGF-β signaling in fatty liver.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  8. Validation of Anticorrelated TGFβ Signaling and Alternative End-Joining DNA Repair Signatures that Predict Response to Genotoxic Cancer Therapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    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

28 authors at 8 institutions in 4 countries.

Jian ChenDepartment of Gastroenterology, Hepatology, and Nutrition, University of Texas MD Anderson Cancer Center, Houston, TX.
Vivek ShuklaDepartment of Gastroenterology, Hepatology, and Nutrition, University of Texas MD Anderson Cancer Center, Houston, TX.
Patrizia FarciHepatic Pathogenesis Section, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD.
Jaclyn AndricovichDepartment of Anatomy and Regenerative Biology, George Washington University, Washington, DC.
Wilma JogunooriInstitute for Clinical Research, Veterans Affairs Medical Center, Washington, DC.
Lawrence N KwongDepartment of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, TX.
Lior H KatzDepartment of Gastroenterology, Hepatology, and Nutrition, University of Texas MD Anderson Cancer Center, Houston, TX.
Kirti ShettyDivision of Gastroenterology and Hepatology, Johns Hopkins University School of Medicine, Baltimore, MD.
Asif RashidDepartment of Pathology, University of Texas MD Anderson Cancer Center, Houston, TX.
Xiaoping SuDepartment of Bioinformatics and Computational Biology, University of Texas MD Anderson Cancer Center, Houston, TX.
Jon WhiteInstitute for Clinical Research, Veterans Affairs Medical Center, Washington, DC.
Lei LiDepartment of Experimental Radiation Oncology, University of Texas MD Anderson Cancer Center, Houston, TX.
Alan Yaoqi WangDepartment of Cancer Biology, University of Texas MD Anderson Cancer Center, Houston, TX.
Boris BlechaczDepartment of Gastroenterology, Hepatology, and Nutrition, University of Texas MD Anderson Cancer Center, Houston, TX.
Gottumukkala S RajuDepartment of Gastroenterology, Hepatology, and Nutrition, University of Texas MD Anderson Cancer Center, Houston, TX.
Marta DavilaDepartment of Gastroenterology, Hepatology, and Nutrition, University of Texas MD Anderson Cancer Center, Houston, TX.
Bao-Ngoc NguyenDepartment of Surgery, George Washington University, Washington, DC.
John R StroehleinDepartment of Gastroenterology, Hepatology, and Nutrition, University of Texas MD Anderson Cancer Center, Houston, TX.
Junjie ChenDepartment of Experimental Radiation Oncology, University of Texas MD Anderson Cancer Center, Houston, TX.
Sang Soo KimNational Cancer Center, Radiation Medicine Branch, Goyang, Korea.
Heather LevinDepartment of Surgery, George Washington University, Washington, DC.
Keigo MachidaSouthern California Research Center for ALPD and Cirrhosis, University of Southern California, Los Angeles, CA.
Hidekazu TsukamotoSouthern California Research Center for ALPD and Cirrhosis, University of Southern California, Los Angeles, CA.
Peter MichaelyDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX.
Alexandros TzatsosDepartment of Anatomy and Regenerative Biology, George Washington University, Washington, DC.
Bibhuti MishraInstitute for Clinical Research, Veterans Affairs Medical Center, Washington, DC.
Richard AmdurDepartment of Surgery, George Washington University, Washington, DC.
Lopa MishraInstitute for Clinical Research, Veterans Affairs Medical Center, Washington, DC.
The University of Texas MD Anderson Cancer Center · USGeorge Washington University · USNational Institute of Allergy and Infectious Diseases · USSouthern California Reproductive Center · USCancer Institute (WIA) · INJohns Hopkins University · USNational Institutes of Health · USSheba Medical Center · IL

Funding

USC RESEARCH CENTER FOR LIVER DISEASES: PILOT PROGRAMSP30DK048522 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI KAPLOWITZ, NEIL · 1995 to 2020
$21.8M
Targeting CDK4 in TGS-B Inactivated Gastrointestinal CancersP01CA130821 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI REDDY, E PREMKUMAR · 2008 to 2013
$6.9M
Role of Beta Spectrin and Smad in Alcohol-Induced Liver and GI Cell ProliferationR01AA023146 · NIAAA · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Lopa Mishra · 2013 to 2026
$4.6M
METASTATIC POTENTIAL OF HUMAN COLORECTAL CARCINOMAR01CA042857 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MISHRA, LOPA · 1986 to 2010
$3.2M
TLR4 and TGF-beta interactions in HCC induced by HCV and alcoholRC2AA019392 · NIAAA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TSUKAMOTO, HIDEKAZU · 2009 to 2010
$1.9M
NANOG-positive cancer stem cells in liver oncogenesis induced by alcohol and HCVR01AA025204 · NIAAA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MACHIDA, KEIGO · 2017 to 2021
$1.9M
Role of epigenetic regulators in pancreatic cancerR00CA158582 · NCI · GEORGE WASHINGTON UNIVERSITY · PI TZATSOS, ALEXANDROS · 2014 to 2016
$707k
Molecular Mechanisms and Translational studies in Colon CancerI01BX003732 · VA · U.S. DEPT/VETS AFFAIRS MEDICAL CENTER · PI MISHRA, LOPA · 2017 to 2019
–
BLRD VA I01 BX003732NCI NIH HHS P01 CA130821NCI NIH HHS R00 CA158582NCI NIH HHS R01 CA042857NIAAA NIH HHS R01 AA023146NIAAA NIH HHS R01 AA025204NIAAA NIH HHS RC2 AA019392NIDDK NIH HHS P30 DK048522
6 · The paper itself

Abstract

Exposure to genotoxins such as ethanol-derived acetaldehyde leads to DNA damage and liver injury and promotes the development of cancer. We report here a major role for the transforming growth factor β/mothers against decapentaplegic homolog 3 adaptor β2-Spectrin (β2SP, gene Sptbn1) in maintaining genomic stability following alcohol-induced DNA damage. β2SP supports DNA repair through β2SP-dependent activation of Fanconi anemia complementation group D2 (Fancd2), a core component of the Fanconi anemia complex. Loss of β2SP leads to decreased Fancd2 levels and sensitizes β2SP mutants to DNA damage by ethanol treatment, leading to phenotypes that closely resemble those observed in animals lacking both aldehyde dehydrogenase 2 and Fancd2 and resemble human fetal alcohol syndrome. Sptbn1-deficient cells are hypersensitive to DNA crosslinking agents and have defective DNA double-strand break repair that is rescued by ectopic Fancd2 expression. Moreover, Fancd2 transcription in response to DNA damage/transforming growth factor β stimulation is regulated by the β2SP/mothers against decapentaplegic homolog 3 complex.

conclusionDysfunctional transforming growth factor β/β2SP signaling impacts the processing of genotoxic metabolites by altering the Fanconi anemia DNA repair pathway. (Hepatology 2017;65:678-693).

Indexed as

Pregnancy, AnimalAnalysis of VarianceAnimalsAnimals, NewbornDNA DamageDNA RepairEthanolFanconi Anemia Complementation Group D2 ProteinFemaleFetal Alcohol Spectrum DisordersGenomic InstabilityHumansImmunohistochemistryLipid PeroxidationMiceMice, TransgenicEthanolFanconi Anemia Complementation Group D2 ProteinSpectrinTransforming Growth Factor beta2

Identifiers

PMID28114741
PMCPMC5432427
OpenAlexW2547904659

What OpenQuestion holds

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Registered trials

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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.