Evidence map›Paper›PMID 31353815›Full record

ArticleMolecular oncology2019

RITA modulates cell migration and invasion by affecting focal adhesion dynamics.

Samira Catharina Hoock, Andreas Ritter, Kerstin Steinhäuser, Susanne Roth, Christian Behrends, Franz Oswald, Christine Solbach, Frank Louwen, Nina-Naomi Kreis, Juping Yuan

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2019. 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
1.2field-weighted citation impact, top 23% 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, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. LncRNA MAFG-AS1 is involved in human cancer progression.European journal of medical research · 2023
    Review
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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

10 authors at 2 institutions in 1 country.

Samira Catharina HoockDepartment of Gynecology and Obstetrics, School of Medicine, J. W. Goethe-University, Frankfurt, Germany.
Andreas RitterDepartment of Gynecology and Obstetrics, School of Medicine, J. W. Goethe-University, Frankfurt, Germany.
Kerstin SteinhäuserDepartment of Gynecology and Obstetrics, School of Medicine, J. W. Goethe-University, Frankfurt, Germany.
Susanne RothDepartment of Gynecology and Obstetrics, School of Medicine, J. W. Goethe-University, Frankfurt, Germany.
Christian BehrendsInstitute of Biochemistry II, Medical School, J. W.-Goethe University, Frankfurt, Germany.
Franz OswaldDepartment of Internal Medicine I, Center for Internal Medicine, Medical Center Ulm, Germany.
Christine SolbachDepartment of Gynecology and Obstetrics, School of Medicine, J. W. Goethe-University, Frankfurt, Germany.
Frank LouwenDepartment of Gynecology and Obstetrics, School of Medicine, J. W. Goethe-University, Frankfurt, Germany.
Nina-Naomi KreisDepartment of Gynecology and Obstetrics, School of Medicine, J. W. Goethe-University, Frankfurt, Germany.
Juping YuanDepartment of Gynecology and Obstetrics, School of Medicine, J. W. Goethe-University, Frankfurt, Germany.ORCID 0000-0003-0694-0565
Goethe University Frankfurt · DEUniversität Ulm · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RITA, the RBP-J interacting and tubulin-associated protein, has been reported to be related to tumor development, but the underlying mechanisms are not understood. Since RITA interacts with tubulin and coats microtubules of the cytoskeleton, we hypothesized that it is involved in cell motility. We show here that depletion of RITA reduces cell migration and invasion of diverse cancer cell lines and mouse embryonic fibroblasts. Cells depleted of RITA display stable focal adhesions (FA) with elevated active integrin, phosphorylated focal adhesion kinase, and paxillin. This is accompanied by enlarged size and disturbed turnover of FA. These cells also demonstrate increased polymerized tubulin. Interestingly, RITA is precipitated with the lipoma-preferred partner (LPP), which is critical in actin cytoskeleton remodeling and cell migration. Suppression of RITA results in reduced LPP and α-actinin at FA leading to compromised focal adhesion turnover and actin dynamics. This study identifies RITA as a novel crucial player in cell migration and invasion by affecting the turnover of FA through its interference with the dynamics of actin filaments and microtubules. Its deregulation may contribute to malignant progression.

Indexed as

AnimalsCell Line, TumorCell MovementDNA-Binding ProteinsFocal AdhesionsGene DeletionHumansMiceMicrotubulesNeoplasm InvasivenessNeoplasm ProteinsNeoplasmsDNA-Binding ProteinsNeoplasm ProteinsZNF331 protein, humanFAKfocal adhesionintegrininvasionLPPRITA

Identifiers

PMID31353815
PMCPMC6763788
OpenAlexW2964430021

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.