Evidence map›Paper›PMID 29854878›Full record

ArticleOncoscience2018

Panobinostat suppresses the mesenchymal phenotype in a novel claudin-low triple negative patient-derived breast cancer model.

Margarite D Matossian, Hope E Burks, Steven Elliott, Van T Hoang, Annie C Bowles, Rachel A Sabol, Bruce A Bunnell, Elizabeth C Martin, Matthew E Burow, Bridgette M Collins-Burow

Abstract read
In one paragraph

Article in Oncoscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Article
  2. Decoding the Epigenome of Breast Cancer.International journal of molecular sciences · 2025
    Review
  3. 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

10 authors.

Margarite D MatossianTulane University School of Medicine, Department of Medicine, Section of Hematology & Medical Oncology, New Orleans LA, USA.
Hope E BurksTulane University School of Medicine, Department of Medicine, Section of Hematology & Medical Oncology, New Orleans LA, USA.
Steven ElliottTulane University School of Medicine, Department of Medicine, Section of Hematology & Medical Oncology, New Orleans LA, USA.
Van T HoangTulane University School of Medicine, Department of Medicine, Section of Hematology & Medical Oncology, New Orleans LA, USA.
Annie C BowlesTulane Center for Stem Cell Research and Regenerative Medicine, New Orleans LA, USA.
Rachel A SabolTulane Center for Stem Cell Research and Regenerative Medicine, New Orleans LA, USA.
Bruce A BunnellTulane Center for Stem Cell Research and Regenerative Medicine, New Orleans LA, USA.
Elizabeth C MartinLouisiana State University, Department of Agricultural Engineering, Baton Rouge LA, USA.
Matthew E BurowTulane University School of Medicine, Department of Medicine, Section of Hematology & Medical Oncology, New Orleans LA, USA.
Bridgette M Collins-BurowTulane University School of Medicine, Department of Medicine, Section of Hematology & Medical Oncology, New Orleans LA, USA.

Funding

Tulane NPRC SPF Sheltered Outdoor Enclosure ExpansionP51OD011104 · OD · TULANE UNIVERSITY OF LOUISIANA · PI L Lee HAMM · 2012 to 2026
$142.4M
Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 2012 to 2026
$69.1M
Kinase mediated suppression of metastasis in breast cancerR01CA174785 · NCI · TULANE UNIVERSITY OF LOUISIANA · PI COLLINS-BUROW, BRIDGETTE MICHELLE · 2016 to 2020
$1.8M
MEK5-Erk5 in breast cancer resistanceR01CA125806 · NCI · TULANE UNIVERSITY OF LOUISIANA · PI BUROW, MATTHEW E. · 2010 to 2014
$1.5M
NCI NIH HHS R01 CA125806NCI NIH HHS R01 CA174785NIGMS NIH HHS U54 GM104940NIH HHS P51 OD011104
6 · The paper itself

Abstract

Claudin-low triple negative breast cancer (CL-TNBC) is a clinically aggressive molecular TNBC subtype characterized by a propensity to metastasize, recur and acquire chemoresistance. CL-TNBC has a diverse intra- and extracellular composition and microenvironment, and currently there are no clinically approved targeted therapies. Histone deacetylase inhibitors (HDACi) have been investigated as therapeutic agents targeting invasive TNBC phenotypes. However, further studies are required to evaluate HDAC inhibition in CL-TNBC. Here, we utilize a novel CL- TNBC patient-derived xenograft model to study the various and diverse therapeutic potential targets within CL-TNBC tumors. To evaluate effects of the pan-HDACi panobinostat on metastasis and the mesenchymal phenotype of CL-TNBC, we utilize immunohistochemistry staining and qRT-PCR in

Indexed as

claudin-lowextracellular matrixhistone deacetylase inhibitorpatient-derived xenografttriple-negative breast cancer

Identifiers

PMID29854878
PMCPMC5978446

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.