Evidence map›Paper›PMID 35585598›Full record

ArticleCell communication and signaling : CCS2022

Optogenetic control of NOTCH1 signaling.

Joanna Kałafut, Jakub Czapiński, Alicja Przybyszewska-Podstawka, Arkadiusz Czerwonka, Adrian Odrzywolski, Cecilia Sahlgren, Adolfo Rivero-Müller

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Cell communication and signaling : CCS, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

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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

7 authors at 2 institutions in 3 countries.

Joanna KałafutDepartment of Biochemistry and Molecular Biology, Medical University of Lublin, 21-093, Lublin, Poland.ORCID 0000-0002-7452-8874
Jakub CzapińskiDepartment of Biochemistry and Molecular Biology, Medical University of Lublin, 21-093, Lublin, Poland.ORCID 0000-0002-0259-2842
Alicja Przybyszewska-PodstawkaDepartment of Biochemistry and Molecular Biology, Medical University of Lublin, 21-093, Lublin, Poland.ORCID 0000-0003-1611-7994
Arkadiusz CzerwonkaDepartment of Biochemistry and Molecular Biology, Medical University of Lublin, 21-093, Lublin, Poland.ORCID 0000-0002-2299-4881
Adrian OdrzywolskiDepartment of Biochemistry and Molecular Biology, Medical University of Lublin, 21-093, Lublin, Poland.ORCID 0000-0002-3370-8801
Cecilia SahlgrenFaculty of Science and Engineering, Biosciences, Åbo Akademi, Turku, Finland.ORCID 0000-0003-3350-4937
Adolfo Rivero-MüllerDepartment of Biochemistry and Molecular Biology, Medical University of Lublin, 21-093, Lublin, Poland. a.rivero@umlub.pl.ORCID 0000-0002-9794-802X
Medical University of Lublin · PLÅbo Akademi University · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Notch signaling pathway is a crucial regulator of cell differentiation as well as tissue organization, whose deregulation is linked to the pathogenesis of different diseases. NOTCH1 plays a key role in breast cancer progression by increasing proliferation, maintenance of cancer stem cells, and impairment of cell death. NOTCH1 is a mechanosensitive receptor, where mechanical force is required to activate the proteolytic cleavage and release of the Notch intracellular domain (NICD). We circumvent this limitation by regulating Notch activity by light. To achieve this, we have engineered an optogenetic NOTCH1 receptor (optoNotch) to control the activation of NOTCH1 intracellular domain (N1ICD) and its downstream transcriptional activities. Using optoNotch we confirm that NOTCH1 activation increases cell proliferation in MCF7 and MDA-MB-468 breast cancer cells in 2D and spheroid 3D cultures, although causing distinct cell-type specific migratory phenotypes. Additionally, optoNotch activation induced chemoresistance on the same cell lines. OptoNotch allows the fine-tuning, ligand-independent, regulation of N1ICD activity and thus a better understanding of the spatiotemporal complexity of Notch signaling. Video Abstract.

Indexed as

Breast NeoplasmsReceptor, Notch1Cell Line, TumorCell ProliferationFemaleHumansMCF-7 CellsOptogeneticsSignal TransductionNOTCH1 protein, humanReceptor, Notch1Breast cancerLight-activationNOTCH1Notch signalingOptogenetics

Identifiers

PMID35585598
PMCPMC9118860
OpenAlexW4280637366

What OpenQuestion holds

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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.