Evidence map›Paper›PMID 33514514›Full record

ArticleCancer research2021

Estrogen Receptor β-Mediated Inhibition of Actin-Based Cell Migration Suppresses Metastasis of Inflammatory Breast Cancer.

Christoforos Thomas, Ilias V Karagounis, Ratnesh K Srivastava, Nicholas Vrettos, Fotis Nikolos, Noëlle Francois, Menggui Huang, Siliang Gong, Qi Long, Sushil Kumar and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2021. 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
0.9field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 14 citations in OpenAlex.

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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

15 authors at 3 institutions in 1 country.

Christoforos Thomas *Department of Radiation Oncology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania. thomaschristoforos@gmail.com Amit.Maity@uphs.upenn.edu.ORCID 0000-0003-3003-2954
Ilias V Karagounis *Department of Radiation Oncology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0003-1642-1996
Ratnesh K SrivastavaDepartment of Biomedical Sciences, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Nicholas VrettosDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Fotis NikolosCedars-Sinai Medical Center, Los Angeles, California.ORCID 0000-0002-8622-0017
Noëlle FrancoisDepartment of Radiation Oncology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Menggui HuangDepartment of Radiation Oncology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Siliang GongDepartment of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Qi LongDepartment of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Sushil KumarDepartment of Biomedical Sciences, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0003-0547-745X
Constantinos KoumenisDepartment of Radiation Oncology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0001-5945-4726
Savitri KrishnamurthyDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Naoto T UenoMorgan Welch Inflammatory Breast Cancer Research Program and Clinic, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0002-0166-7275
Rumela ChakrabartiDepartment of Biomedical Sciences, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0001-7720-9660
Amit MaityDepartment of Radiation Oncology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania. thomaschristoforos@gmail.com Amit.Maity@uphs.upenn.edu.
University of Pennsylvania · USThe University of Texas MD Anderson Cancer Center · USCedars-Sinai Medical Center · US

Funding

Exploring the role of estrogen receptor beta in progression and metastasis ofInflammatory breast cancerR01CA237200 · NCI · UNIVERSITY OF PENNSYLVANIA · PI THOMAS, CHRISTOFOROS · 2020 to 2024
$1.8M
Improving radiation response by targeting O2 metabolism via the PI3K/mTOR pathwayR01CA182747 · NCI · UNIVERSITY OF PENNSYLVANIA · PI KOUMENIS, CONSTANTINOS, MAITY, AMIT · 2015 to 2019
$1.8M
Exploring the role of ER Beta in disease penetrance in individuals with Li-Fraumeni syndromeR21CA267386 · NCI · UNIVERSITY OF PENNSYLVANIA · PI THOMAS, CHRISTOFOROS · 2022 to 2023
$395k
NCI NIH HHS R01 CA182747NCI NIH HHS R01 CA237200NCI NIH HHS R21 CA267386
6 · The paper itself

Abstract

Inflammatory breast cancer (IBC) is a highly metastatic breast carcinoma with high frequency of estrogen receptor α (ERα) negativity. Here we explored the role of the second ER subtype, ERβ, and report expression in IBC tumors and its correlation with reduced metastasis. Ablation of ERβ in IBC cells promoted cell migration and activated gene networks that control actin reorganization, including G-protein-coupled receptors and downstream effectors that activate Rho GTPases. Analysis of preclinical mouse models of IBC revealed decreased metastasis of IBC tumors when ERβ was expressed or activated by chemical agonists. Our findings support a tumor-suppressive role of ERβ by demonstrating the ability of the receptor to inhibit dissemination of IBC cells and prevent metastasis. On the basis of these findings, we propose ERβ as a potentially novel biomarker and therapeutic target that can inhibit IBC metastasis and reduce its associated mortality. SIGNIFICANCE: These findings demonstrate the capacity of ERβ to elicit antimetastatic effects in highly aggressive inflammatory breast cancer and propose ERβ and the identified associated genes as potential therapeutic targets in this disease.

Indexed as

Actin CytoskeletonActinsAnimalsCell MovementCohort StudiesEstrogen Receptor alphaEstrogen Receptor betaFemaleGene Knockout TechniquesHEK293 CellsHumansInflammatory Breast NeoplasmsMCF-7 CellsMiceNeoplasm MetastasisSignal TransductionActinsESR1 protein, humanESR2 protein, humanEstrogen Receptor alphaEstrogen Receptor beta

Identifiers

PMID33514514
PMCPMC8570087
OpenAlexW3123998903

What OpenQuestion holds

Textmetadata
LicenceTDM
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.