Evidence map›Paper›PMID 34531530›Full record

ArticleCommunications biology2021

TC10 regulates breast cancer invasion and metastasis by controlling membrane type-1 matrix metalloproteinase at invadopodia.

Maren Hülsemann, Colline Sanchez, Polina V Verkhusha, Vera Des Marais, Serena P H Mao, Sara K Donnelly, Jeffrey E Segall, Louis Hodgson

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Communications biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 40% 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

8 citing papers in PubMed, 8 citations in OpenAlex.

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  8. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Maren HülsemannDepartment of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Colline SanchezDepartment of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Polina V VerkhushaDepartment of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Vera Des MaraisDepartment of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Serena P H MaoDepartment of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Sara K DonnellyDepartment of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.ORCID http://orcid.org/0000-0002-4844-8694
Jeffrey E SegallDepartment of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Louis HodgsonDepartment of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA. louis.hodgson@einsteinmed.org.ORCID http://orcid.org/0000-0001-9188-7580
Albert Einstein College of Medicine · US

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI STEVEN C. ALMO · 1985 to 2026
$111.2M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007288 · NIGMS · YESHIVA UNIVERSITY · PI AKABAS, MYLES H. · 1985 to 2022
$35.6M
Tumor Progression and MetastasisP01CA100324 · NCI · YESHIVA UNIVERSITY · PI CONDEELIS, JOHN S · 2003 to 2018
$30.0M
Multiplex Imaging of Signaling Pathways in Cell MotilityR35GM136226 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI Louis Hodgson · 2020 to 2026
$5.3M
Super Resolution PALM/STORM Microscopy System In Multi-User FacilityS10OD018218 · OD · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI VERKHUSHA, VLADISLAV · 2014 to 2014
$501k
American Cancer Society (American Cancer Society, Inc.) PF-15-135-01-CSMNCI NIH HHS P01 CA100324NCI NIH HHS P30 CA013330NIGMS NIH HHS R35 GM136226NIGMS NIH HHS T32 GM007288NIH HHS S10 OD018218U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) CA100324
6 · The paper itself

Abstract

During breast cancer metastasis, cancer cell invasion is driven by actin-rich protrusions called invadopodia, which mediate the extracellular matrix degradation required for the success of the invasive cascade. In this study, we demonstrate that TC10, a member of a Cdc42 subfamily of p21 small GTPases, regulates the membrane type 1 matrix metalloproteinase (MT1-MMP)-driven extracellular matrix degradation at invadopodia. We show that TC10 is required for the plasma membrane surface exposure of MT1-MMP at these structures. By utilizing our Förster resonance energy transfer (FRET) biosensor, we demonstrate the p190RhoGAP-dependent regulation of spatiotemporal TC10 activity at invadopodia. We identified a pathway that regulates invadopodia-associated TC10 activity and function through the activation of p190RhoGAP and the downstream interacting effector Exo70. Our findings reveal the role of a previously unknown regulator of vesicular fusion at invadopodia, TC10 GTPase, in breast cancer invasion and metastasis.

Indexed as

AdenocarcinomaAnimalsBreast NeoplasmsCell Line, TumorFemaleHumansMammary Neoplasms, AnimalMatrix Metalloproteinase 14MiceMice, SCIDNeoplasm InvasivenessNeoplasm MetastasisRatsrho GTP-Binding ProteinsMatrix Metalloproteinase 14MMP14 protein, humanMmp14 protein, ratrho GTP-Binding ProteinsRHOQ protein, humanRhoq protein, rat

Identifiers

PMID34531530
PMCPMC8445963
OpenAlexW3199085995

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.