Evidence map›Paper›PMID 32518680›Full record

ArticleFuture science OA2020

PTPIP51 crosslinks the NFκB signaling and the MAPK pathway in SKBR3 cells.

Eric Dietel, Alexander Brobeil, Claudia Tag, Stefan Gattenloehner, Monika Wimmer

Open access · goldAbstract read
In one paragraph

Article in Future science OA, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 51% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

5 authors at 2 institutions in 2 countries.

Eric DietelInstitute of Anatomy & Cell Biology, Justus-Liebig-University, Giessen 35392, Germany.ORCID https://orcid.org/0000-0001-7518-8691
Alexander BrobeilInstitute of Pathology, Justus-Liebig-University, Giessen 35392, Germany.
Claudia TagInstitute of Anatomy & Cell Biology, Justus-Liebig-University, Giessen 35392, Germany.
Stefan GattenloehnerInstitute of Pathology, Justus-Liebig-University, Giessen 35392, Germany.
Monika WimmerInstitute of Anatomy & Cell Biology, Justus-Liebig-University, Giessen 35392, Germany.
Justus-Liebig-Universität Gießen · DEJohannes Kepler University of Linz · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimPTPIP51 interacts with NFκB signaling at the RelA and IκB level. NFκB signaling is linked to the initiation, progression and metastasis of breast cancer. Her2-amplified breast cancer cells frequently display activation of the NFκB signaling. We aimed to clarify the effects of NFκB inhibition on the NFκB- and MAPK-related interactome of PTPIP51 and cell viability in HaCat cells and SKBR3 cells.

resultsIKK-16 selectively reduced cell viability in SKBR3 cells. PDTC induced a formation of the Raf1/14-3-3/PTPIP51 complex in SKBR3 cells, indicating a shift of PTPIP51 into MAPK signaling.

conclusionIKK-16 selectively inhibits cell viability of SKBR3 cells. In addition, PTPIP51 might serve as the mediator between NFκB signaling and the MAPK pathway in SKBR3.

Indexed as

breast cancerHer2IKK-16NFκBPDTCprotein–protein interactionsPTPIP51

Identifiers

PMID32518680
PMCPMC7273389
OpenAlexW3010496665

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.