Evidence map›Paper›PMID 27780223›Full record

ArticlePloS one2016

LIM-Only Protein 4 (LMO4) and LIM Domain Binding Protein 1 (LDB1) Promote Growth and Metastasis of Human Head and Neck Cancer (LMO4 and LDB1 in Head and Neck Cancer).

Elizabeth A Simonik, Ying Cai, Katherine N Kimmelshue, Dana M Brantley-Sieders, Holli A Loomans, Claudia D Andl, Grant M Westlake, Victoria M Youngblood, Jin Chen, Wendell G Yarbrough and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
1.1field-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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
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  12. Prospective Advances in Genome Editing Investigation.Advances in experimental medicine and biology · 2023
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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

13 authors at 3 institutions in 1 country.

Elizabeth A SimonikDepartment of Cancer Biology, Vanderbilt University Medical Center, Nashville, TN, United States of America.
Ying CaiDepartment of Cancer Biology, Vanderbilt University Medical Center, Nashville, TN, United States of America.
Katherine N KimmelshueDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN, United States of America.
Dana M Brantley-SiedersDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN, United States of America.
Holli A LoomansDepartment of Cancer Biology, Vanderbilt University Medical Center, Nashville, TN, United States of America.
Claudia D AndlDepartment of Cancer Biology, Vanderbilt University Medical Center, Nashville, TN, United States of America.
Grant M WestlakeDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN, United States of America.
Victoria M YoungbloodDepartment of Cancer Biology, Vanderbilt University Medical Center, Nashville, TN, United States of America.
Jin ChenDepartment of Cancer Biology, Vanderbilt University Medical Center, Nashville, TN, United States of America.
Wendell G YarbroughDepartment of Otolaryngology and Barry Baker Laboratory for Head and Neck Oncology, Vanderbilt University School of Medicine, Nashville, TN, United States of America.
Brandee T BrownDepartment of Otolaryngology and Barry Baker Laboratory for Head and Neck Oncology, Vanderbilt University School of Medicine, Nashville, TN, United States of America.
Lalitha NagarajanDepartment of Genetics, University of Texas M.D. Anderson Cancer Center, Houston, TX, United States of America.
Stephen J BrandtDepartment of Cancer Biology, Vanderbilt University Medical Center, Nashville, TN, United States of America.
Vanderbilt University Medical Center · USThe University of Texas MD Anderson Cancer Center · USVanderbilt University · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MATTHEW J TYSKA · 1995 to 2026
$172.8M
MULTIDISCIPLINARY BASIC RESEARCH TRAINING IN CANCERT32CA009592 · NCI · VANDERBILT UNIVERSITY · PI Justin M Balko, Julie A Rhoades (Sterling) · 1987 to 2026
$10.4M
The role of Activin A signaling in esophageal cell invasionR01DK094900 · NIDDK · VANDERBILT UNIVERSITY · PI ANDL, CLAUDIA D · 2012 to 2016
$1.6M
EphA2 Receptor in Endothelial Cell-Mediated Tumor ProgressionR01CA148934 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BRANTLEY-SIEDERS, DANA M · 2011 to 2015
$1.6M
NCI NIH HHS P30 CA068485NCI NIH HHS R01 CA148934NCI NIH HHS T32 CA009592NIDDK NIH HHS R01 DK094900
6 · The paper itself

Abstract

Squamous cell carcinoma of the head and neck (HNSCC) accounts for more than 300,000 deaths worldwide per year as a consequence of tumor cell invasion of adjacent structures or metastasis. LIM-only protein 4 (LMO4) and LIM-domain binding protein 1 (LDB1), two directly interacting transcriptional adaptors that have important roles in normal epithelial cell differentiation, have been associated with increased metastasis, decreased differentiation, and shortened survival in carcinoma of the breast. Here, we implicate two LDB1-binding proteins, single-stranded binding protein 2 (SSBP2) and 3 (SSBP3), in controlling LMO4 and LDB1 protein abundance in HNSCC and in regulating specific tumor cell functions in this disease. First, we found that the relative abundance of LMO4, LDB1, and the two SSBPs correlated very significantly in a panel of human HNSCC cell lines. Second, expression of these proteins in tumor primaries and lymph nodes involved by metastasis were concordant in 3 of 3 sets of tissue. Third, using a Matrigel invasion and organotypic reconstruct assay, CRISPR/Cas9-mediated deletion of LDB1 in the VU-SCC-1729 cell line, which is highly invasive of basement membrane and cellular monolayers, reduced tumor cell invasiveness and migration, as well as proliferation on tissue culture plastic. Finally, inactivation of the LDB1 gene in these cells decreased growth and vascularization of xenografted human tumor cells in vivo. These data show that LMO4, LDB1, and SSBP2 and/or SSBP3 regulate metastasis, proliferation, and angiogenesis in HNSCC and provide the first evidence that SSBPs control LMO4 and LDB1 protein abundance in a cancer context.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCarcinoma, Squamous CellCell Line, TumorCell MovementCell ProliferationDNA-Binding ProteinsGene Expression Regulation, NeoplasticHumansLIM Domain ProteinsMiceMouth NeoplasmsNeoplasm MetastasisNeoplasm TransplantationTissue Culture TechniquesTranscription FactorsAdaptor Proteins, Signal TransducingDNA-Binding ProteinsLDB1 protein, humanLIM Domain ProteinsLMO4 protein, humanSSBP2 protein, humanSSBP3 protein, humanTranscription Factors

Identifiers

PMID27780223
PMCPMC5079595
OpenAlexW2536936441

What OpenQuestion holds

Textmetadata
LicenceCC0
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.