Evidence map›Paper›PMID 32051509›Full record

ArticleScientific reports2020

The scaffold protein IQGAP1 is crucial for extravasation and metastasis.

Jess D Hebert, Chenxi Tian, John M Lamar, Steffen Rickelt, Genevieve Abbruzzese, Xiaotie Liu, Richard O Hynes

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. 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
0.7field-weighted citation impact, top 29% 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, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. AmotL2, IQGAP1, and FKBP51 Scaffold Proteins in Glioblastoma Stem Cell Niches.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2022
    Review
  10. Inhibition of induced-hepatic cancerFrontiers in oncology · 2022
    Article
  11. Review
  12. Article
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 2 institutions in 1 country.

Jess D HebertDepartment of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, 02139, USA.ORCID https://orcid.org/0000-0002-8778-5941
Chenxi TianKoch Institute for Integrated Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts, 02139, USA.
John M LamarKoch Institute for Integrated Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts, 02139, USA.ORCID http://orcid.org/0000-0001-5406-8391
Steffen RickeltKoch Institute for Integrated Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts, 02139, USA.ORCID http://orcid.org/0000-0002-5224-7764
Genevieve AbbruzzeseKoch Institute for Integrated Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts, 02139, USA.ORCID http://orcid.org/0000-0002-3194-9353
Xiaotie LiuKoch Institute for Integrated Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts, 02139, USA.
Richard O HynesDepartment of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, 02139, USA. rohynes@mit.edu.ORCID https://orcid.org/0000-0001-7603-8396
Massachusetts Institute of Technology · USHoward Hughes Medical Institute · US

Funding

PRE-DOCTORAL TRAINING IN THE BIOLOGICAL SCIENCEST32GM007287 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BELL, STEPHEN P., KEATING, AMY E · 1985 to 2019
$40.8M
NIGMS NIH HHS T32 GM007287
6 · The paper itself

Abstract

IQGAP1 is a scaffold protein involved in a range of cellular activities, including migration, invasion, adhesion and proliferation. It is also oncogenic in a variety of cancers, promoting primary tumor growth and invasiveness. However, the role of IQGAP1 in tumor progression and metastasis remains unclear. In this study, we use both knockdown and knockout of IQGAP1 to investigate its role in the metastatic cascade of both melanoma and breast cancer cells in vivo. We find that reduction of IQGAP1 expression decreases the formation of both spontaneous and experimental metastases, without limiting primary or metastatic tumor growth. Furthermore, IQGAP1 knockout significantly inhibits extravasation of tumor cells from circulation, possibly involving invadopodial function. By expressing mutant forms of IQGAP1 in a knockout context, we also determine that IQGAP1's pro-metastatic functions are dependent on multiple domains and functions. These data demonstrate that IQGAP1 is crucial for metastasis in vivo through regulation of extravasation and suggest that it may represent a valid therapeutic target for inhibiting metastasis.

Indexed as

Breast NeoplasmsCell Line, TumorCell MovementFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesGene Knockout TechniquesHumansMelanomaNeoplasm InvasivenessNeoplasm Metastasisras GTPase-Activating ProteinsIQ motif containing GTPase activating protein 1ras GTPase-Activating Proteins

Identifiers

PMID32051509
PMCPMC7015931
OpenAlexW3006299474

What OpenQuestion holds

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LicenceCC BY
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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.