Evidence map›Paper›PMID 36230774›Full record

ArticleCancers2022

FOXC2 Promotes Vasculogenic Mimicry in Ovarian Cancer.

Maria Sol Recouvreux, Jiangyong Miao, Maricel C Gozo, Jingni Wu, Ann E Walts, Beth Y Karlan, Sandra Orsulic

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

9 citing papers in PubMed, 31 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

7 authors at 3 institutions in 1 country.

Maria Sol RecouvreuxDepartment of Obstetrics and Gynecology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA.ORCID 0000-0002-8064-9381
Jiangyong MiaoDepartment of Pathology, Massachusetts General Hospital, Boston, MA 02114, USA.
Maricel C GozoWomen's Cancer Program, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
Jingni WuDepartment of Obstetrics and Gynecology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA.
Ann E WaltsDepartment of Pathology and Laboratory Medicine, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
Beth Y KarlanDepartment of Obstetrics and Gynecology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA.
Sandra OrsulicDepartment of Obstetrics and Gynecology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA.ORCID 0000-0001-5119-8721
University of California, Los Angeles · USCedars-Sinai Medical Center · USMassachusetts General Hospital · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Robert Damoiseaux · 1985 to 2026
$134.5M
Cancer-Associated Fibroblasts Alter the Composition of B Cells I Solid Malignancies - Diversity SupplementR01CA208753 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ORSULIC, SANDRA · 2016 to 2020
$2.2M
Precancer Niche Formation in the Fallopian TubeI01BX004974 · VA · VA GREATER LOS ANGELES HEALTHCARE SYSTEM · PI ORSULIC, SANDRA · 2020 to 2024
–
BLRD VA I01 BX004974NCI NIH HHS P30 CA016042NCI NIH HHS R01 CA208753NIH HHS R01 CA208753
6 · The paper itself

Abstract

FOXC2 is a forkhead family transcription factor that plays a critical role in specifying mesenchymal cell fate during embryogenesis. FOXC2 expression is associated with increased metastasis and poor survival in various solid malignancies. Using in vitro and in vivo assays in mouse ovarian cancer cell lines, we confirmed the previously reported mechanisms by which FOXC2 could promote cancer growth, metastasis, and drug resistance, including epithelial-mesenchymal transition, stem cell-like differentiation, and resistance to anoikis. In addition, we showed that FOXC2 expression is associated with vasculogenic mimicry in mouse and human ovarian cancers. FOXC2 overexpression increased the ability of human ovarian cancer cells to form vascular-like structures in vitro, while inhibition of FOXC2 had the opposite effect. Thus, we present a novel mechanism by which FOXC2 might contribute to cancer aggressiveness and poor patient survival.

Indexed as

angiogenesisepithelial-mesenchymal transitionFOXC2mesenchymal cellsovarian cancer progressionstem cellsvascularvasculogenesisvasculogenic mimicry

Identifiers

PMID36230774
PMCPMC9564305
OpenAlexW4303621958

What Socratic 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 Socratic graph.