Evidence map›Paper›PMID 33202906›Full record

ArticleCancers2020

ShcD Binds DOCK4, Promotes Ameboid Motility and Metastasis Dissemination, Predicting Poor Prognosis in Melanoma.

Ewa Aladowicz, Letizia Granieri, Federica Marocchi, Simona Punzi, Giuseppina Giardina, Pier Francesco Ferrucci, Giovanni Mazzarol, Maria Capra, Giuseppe Viale, Stefano Confalonieri and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
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 5 institutions in 2 countries.

Ewa AladowiczSarcoma Molecular Pathology Team, Divisions of Molecular Pathology and Cancer Therapeutics, The Institute of Cancer Research (ICR), 15 Cotswold Road, Sutton SM2 5NG, UK.
Letizia GranieriDepartment of Experimental Oncology, European Institute of Oncology IRCCS (IEO), Via Adamello, 16, 20139 Milan, Italy.
Federica MarocchiDepartment of Experimental Oncology, European Institute of Oncology IRCCS (IEO), Via Adamello, 16, 20139 Milan, Italy.
Simona PunziDepartment of Experimental Oncology, European Institute of Oncology IRCCS (IEO), Via Adamello, 16, 20139 Milan, Italy.ORCID 0000-0002-8734-6404
Giuseppina GiardinaDepartment of Experimental Oncology, European Institute of Oncology IRCCS (IEO), Via Adamello, 16, 20139 Milan, Italy.
Pier Francesco FerrucciDepartment of Experimental Oncology, European Institute of Oncology IRCCS (IEO), Via Adamello, 16, 20139 Milan, Italy.ORCID 0000-0001-6255-5851
Giovanni MazzarolDivision of Pathology, European Institute of Oncology IRCCS (IEO), Via Ripamonti 435, 20141 Milan, Italy.
Maria CapraDivision of Pathology, European Institute of Oncology IRCCS (IEO), Via Ripamonti 435, 20141 Milan, Italy.
Giuseppe VialeDivision of Pathology, European Institute of Oncology IRCCS (IEO), Via Ripamonti 435, 20141 Milan, Italy.
Stefano ConfalonieriDepartment of Experimental Oncology, European Institute of Oncology IRCCS (IEO), Via Adamello, 16, 20139 Milan, Italy.ORCID 0000-0001-6886-9851
Sara GandiniDepartment of Experimental Oncology, European Institute of Oncology IRCCS (IEO), Via Adamello, 16, 20139 Milan, Italy.
Fiorenza LottiDepartment of Experimental Oncology, European Institute of Oncology IRCCS (IEO), Via Adamello, 16, 20139 Milan, Italy.
Luisa LanfranconeDepartment of Experimental Oncology, European Institute of Oncology IRCCS (IEO), Via Adamello, 16, 20139 Milan, Italy.ORCID 0000-0002-4523-3815
European Institute of Oncology · ITRipamonti · ITCandiolo Cancer Institute · ITInstitute of Cancer Research · GBUniversity of Milan · IT

Funding

Associazione Italiana per la Ricerca sul Cancro Id 20508
6 · The paper itself

Abstract

Metastases are the primary cause of cancer-related deaths. The underlying molecular and biological mechanisms remain, however, elusive, thus preventing the design of specific therapies. In melanomas, the metastatic process is influenced by the acquisition of metastasis-associated mutational and epigenetic traits and the activation of metastatic-specific signaling pathways in the primary melanoma. In the current study, we investigated the role of an adaptor protein of the Shc family (ShcD) in the acquisition of metastatic properties by melanoma cells, exploiting our cohort of patient-derived xenografts (PDXs). We provide evidence that the depletion of ShcD expression increases a spread cell shape and the capability of melanoma cells to attach to the extracellular matrix while its overexpression switches their morphology from elongated to rounded on 3D matrices, enhances cells' invasive phenotype, as observed on collagen gel, and favors metastasis formation in vivo. ShcD overexpression sustains amoeboid movement in melanoma cells, by suppressing the Rac1 signaling pathway through the confinement of DOCK4 in the cytoplasm. Inactivation of the ShcD signaling pathway makes melanoma cells more sensitive to therapeutic treatments. Consistently, ShcD expression predicts poor outcome in a cohort of 183 primary melanoma patients.

Indexed as

amoeboid motilityDOCK4melanoma metastasismelanoma PDXRac1ShcD adaptor protein

Identifiers

PMID33202906
PMCPMC7696252
OpenAlexW3101459291

What OpenQuestion holds

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Registered trials

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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.