Evidence map›Paper›PMID 35261806›Full record

ArticleAmerican journal of cancer research2022

Depletion of CCN1/CYR61 reduces triple-negative/basal-like breast cancer aggressiveness.

Ingrid Espinoza, Chandra Kurapaty, Cheol-Hong Park, Travis Vander Steen, Celina G Kleer, Elizabeth Wiley, Alfred Rademaker, Elisabet Cuyàs, Sara Verdura, Maria Buxó and 3 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 16 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

13 authors at 6 institutions in 2 countries.

Ingrid EspinozaDivision of Experimental Pathology, Department of Laboratory Medicine and Pathology, Mayo Clinic Rochester, MN 55905, USA.
Chandra KurapatyDivision of Experimental Pathology, Department of Laboratory Medicine and Pathology, Mayo Clinic Rochester, MN 55905, USA.
Cheol-Hong ParkDivision of Experimental Pathology, Department of Laboratory Medicine and Pathology, Mayo Clinic Rochester, MN 55905, USA.
Travis Vander SteenDivision of Experimental Pathology, Department of Laboratory Medicine and Pathology, Mayo Clinic Rochester, MN 55905, USA.
Celina G KleerDepartment of Pathology, University of Michigan Ann Arbor, MI 48109, USA.
Elizabeth WileyDepartment of Pathology, University of Illinois at Chicago Chicago, IL 60607, USA.
Alfred RademakerDepartment of Preventive Medicine, Northwestern University Feinberg School of Medicine Chicago, IL 60611, USA.
Elisabet CuyàsGirona Biomedical Research Institute 17190 Salt, Girona, Spain.
Sara VerduraGirona Biomedical Research Institute 17190 Salt, Girona, Spain.
Maria BuxóStatistical and Methodological Advice Unit, Girona Biomedical Research Institute 17190 Salt, Girona, Spain.
Carol ReynoldsDepartment of Pathology, Division of Anatomic Pathology, Mayo Clinic Rochester, MN 55905, USA.
Javier A MenendezGirona Biomedical Research Institute 17190 Salt, Girona, Spain.
Ruth LupuDivision of Experimental Pathology, Department of Laboratory Medicine and Pathology, Mayo Clinic Rochester, MN 55905, USA.
Mayo Clinic · USUniversitat de Girona · ESClínica Girona · ESNorthwestern University · USUniversity of Illinois Chicago · USUniversity of Michigan · US

Funding

Role of CCN6 (WISP3) in the Progression and Metastasis of Breast Cancer.R01CA125577 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Celina G Kleer · 2008 to 2026
$5.5M
Fatty Acid Synthase:Molecular Target for Breast Cancer Therapy & ChemopreventionR01CA116623 · NCI · NORTHSHORE UNIV HEALTHSYSTEM RES INST · PI LUPU, RUTH · 2005 to 2014
$3.4M
Cyr61-induced breast cancer: Clinical relevance and therapeutic developmentR01CA118975 · NCI · NORTHSHORE UNIVERSITY HEALTHSYSTEM · PI LUPU, RUTH · 2006 to 2010
$1.5M
NCI NIH HHS R01 CA116623NCI NIH HHS R01 CA118975NCI NIH HHS R01 CA125577
6 · The paper itself

Abstract

Triple-negative/basal-like breast cancer (BC) is characterized by aggressive biological features, which allow relapse and metastatic spread to occur more frequently than in hormone receptor-positive (luminal) subtypes. The molecular complexity of triple-negative/basal-like BC poses major challenges for the implementation of targeted therapies, and chemotherapy remains the standard approach at all stages. The matricellular protein cysteine-rich angiogenic inducer 61 (CCN1/CYR61) is associated with aggressive metastatic phenotypes and poor prognosis in BC, but it is unclear whether anti-CCN1 approaches can be successfully applied in triple-negative/basal-like BC. Herein, we first characterized the prevalence of CNN1 expression in matched samples of primary tumors and metastatic relapse in a series of patients with BC. We then investigated the biological effect of CCN1 depletion on tumorigenic traits

Indexed as

basal-likebreast cancerCCN1integrinsmetastasistriple-negative

Identifiers

PMID35261806
PMCPMC8899977
OpenAlexW4226139743

What OpenQuestion holds

Textmetadata
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.