Evidence map›Paper›PMID 34658143›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2021

Impact of the Nuclear Envelope on Malignant Transformation, Motility, and Survival of Lung Cancer Cells.

Sílvio Terra Stefanello, Isabelle Luchtefeld, Ivan Liashkovich, Zoltan Pethö, Ihab Azzam, Etmar Bulk, Gonzalo Rosso, Lilly Döhlinger, Bettina Hesse, Andrea Oeckinghaus and 1 more

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

13 citing papers in PubMed, 18 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

11 authors at 1 institution in 1 country.

Sílvio Terra StefanelloInstitute of Physiology II, University of Münster, Robert-Koch-Str. 27b, Münster, 48149, Germany.ORCID 0000-0002-6673-6550
Isabelle LuchtefeldInstitute of Physiology II, University of Münster, Robert-Koch-Str. 27b, Münster, 48149, Germany.
Ivan LiashkovichInstitute of Physiology II, University of Münster, Robert-Koch-Str. 27b, Münster, 48149, Germany.
Zoltan PethöInstitute of Physiology II, University of Münster, Robert-Koch-Str. 27b, Münster, 48149, Germany.
Ihab AzzamInstitute of Immunology, University of Münster, Röntgen-Str. 21, Münster, 48149, Germany.
Etmar BulkInstitute of Physiology II, University of Münster, Robert-Koch-Str. 27b, Münster, 48149, Germany.
Gonzalo RossoInstitute of Physiology II, University of Münster, Robert-Koch-Str. 27b, Münster, 48149, Germany.
Lilly DöhlingerInstitute of Physiology II, University of Münster, Robert-Koch-Str. 27b, Münster, 48149, Germany.
Bettina HesseInstitute of Physiology II, University of Münster, Robert-Koch-Str. 27b, Münster, 48149, Germany.
Andrea OeckinghausInstitute of Molecular Tumor Biology, University of Münster, Robert-Koch-Str. 43, Münster, 48149, Germany.
Victor ShahinInstitute of Physiology II, University of Münster, Robert-Koch-Str. 27b, Münster, 48149, Germany.ORCID 0000-0003-2710-6473
University of Münster · DE

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior and Alexander von Humboldt-Stiftung 88881.197729/2018-01Deutsche Forschungsgemeinschaft GRK 2515/1Deutsche Forschungsgemeinschaft LI 2157/3-1Deutsche Forschungsgemeinschaft OE 531/2-2Deutsche Forschungsgemeinschaft SH 167/6-1Deutsche Forschungsgemeinschaft SH 167/6-2Deutsche Forschungsgemeinschaft SH 167/9-1Marie Skłodowska-Curie Innovative Training Network 813834Marie Skłodowska-Curie Innovative Training Network H2020-MSCA-ITN-2018
6 · The paper itself

Abstract

Nuclear pore complexes (NPCs) selectively mediate all nucleocytoplasmic transport and engage in fundamental cell-physiological processes. It is hypothesized that NPCs are critical for malignant transformation and survival of lung cancer cells, and test the hypothesis in lowly and highly metastatic non-small human lung cancer cells (NSCLCs). It is shown that malignant transformation is paralleled by an increased NPCs density, and a balanced pathological weakening of the physiological stringency of the NPC barrier. Pharmacological interference using barrier-breaking compounds collapses the stringency. Concomitantly, it induces drastic overall structural changes of NSCLCs, terminating their migration. Moreover, the degree of malignancy is found to be paralleled by substantially decreased lamin A/C levels. The latter provides crucial structural and mechanical stability to the nucleus, and interacts with NPCs, cytoskeleton, and nucleoskeleton for cell maintenance, survival, and motility. The recent study reveals the physiological importance of the NPC barrier stringency for mechanical and structural resilience of normal cell nuclei. Hence, reduced lamin A/C levels in conjunction with controlled pathological weakening of the NPC barrier stringency may facilitate deformability of NSCLCs during the metastasis steps. Modulation of the NPC barrier presents a potential strategy for suppressing the malignant phenotype or enhancing the effectiveness of currently existing chemotherapeutics.

Indexed as

Active Transport, Cell NucleusAnimalsCell NucleusCell SurvivalDisease Models, AnimalHumansLung NeoplasmsMiceNuclear EnvelopeNuclear Porecancercellular physiology and biophysicsnanomedicinenuclear envelopenuclear pores

Identifiers

PMID34658143
PMCPMC8596107
OpenAlexW3207207184

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.