Evidence map›Paper›PMID 30158824›Full record

ArticleBreast cancer : basic and clinical research2018

Formin Proteins FHOD1 and INF2 in Triple-Negative Breast Cancer: Association With Basal Markers and Functional Activities.

Vanina D Heuser, Naziha Mansuri, Jasper Mogg, Samu Kurki, Heli Repo, Pauliina Kronqvist, Olli Carpén, Maria Gardberg

Open access · goldAbstract read
In one paragraph

Article in Breast cancer : basic and clinical research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
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  11. Role of formin INF2 in human diseases.Molecular biology reports · 2022
    Review
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  15. Review
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  18. The formin INF2 in disease: progress from 10 years of research.Cellular and molecular life sciences : CMLS · 2020
    Review
  19. 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

8 authors at 4 institutions in 2 countries.

Vanina D HeuserInstitute of Biomedicine, University of Turku, Turku, Finland.
Naziha MansuriInstitute of Biomedicine, University of Turku, Turku, Finland.
Jasper MoggNorthern Institute for Cancer Research, Newcastle University, Newcastle-upon-Tyne, UK.
Samu KurkiAuria Biobank, Turku University Hospital and University of Turku, Turku, Finland.
Heli RepoInstitute of Biomedicine, University of Turku, Turku, Finland.
Pauliina KronqvistInstitute of Biomedicine, University of Turku, Turku, Finland.
Olli CarpénInstitute of Biomedicine, University of Turku, Turku, Finland.
Maria GardbergInstitute of Biomedicine, University of Turku, Turku, Finland.
Turku University Hospital · FIUniversity of Turku · FINewcastle University · GBUniversity of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Basal-like breast cancer is an aggressive form of breast cancer with limited treatment options. The subgroup can be identified immunohistochemically, by lack of hormone receptor expression combined with expression of basal markers such as CK5/6 and/or epidermal growth factor receptor (EGFR). In vitro, several regulators of the actin cytoskeleton are essential for efficient invasion of basal-like breast cancer cell lines. Whether these proteins are expressed in vivo determines the applicability of these findings in clinical settings. The actin-regulating formin protein FHOD1 participates in invasion of the triple-negative breast cancer cell line MDA-MB-231. Here, we measure the expression of FHOD1 protein in clinical triple-negative breast cancers by using immunohistochemistry and further characterize the expression of another formin protein, INF2. We report that basal-like breast cancers frequently overexpress formin proteins FHOD1 and INF2. In cell studies using basal-like breast cancer cell lines, we show that knockdown of FHOD1 or INF2 interferes with very similar processes: maintenance of cell shape, migration, invasion, and proliferation. Inhibition of EGFR, PI3K, or mitogen-activated protein kinase activity does not alter the expression of FHOD1 and INF2 in these cell lines. We conclude that the experimental studies on these formins have implications in the clinical behavior of basal-like breast cancer.

Indexed as

actinbasal-like breast cancerBT-549cytoskeletonFHOD1ForminINF2MDA-MB-231triple-negative breast cancer

Identifiers

PMID30158824
PMCPMC6109849
OpenAlexW2888499267

What OpenQuestion holds

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LicenceCC BY-NC
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.