Evidence map›Paper›PMID 30959888›Full record

ArticleCells2019

CRISP-R/Cas9 Mediated Deletion of Copper Transport Genes CTR1 and DMT1 in NSCLC Cell Line H1299. Biological and Pharmacological Consequences.

Ekaterina Y Ilyechova, Elisa Bonaldi, Iurii A Orlov, Ekaterina A Skomorokhova, Ludmila V Puchkova, Massimo Broggini

Open access · goldAbstract read
In one paragraph

Article in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
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  3. Article
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  5. The pathogenesis of liver fibrosis in Wilson's disease: hepatocyte injury and regulation mediated by copper metabolism dysregulation.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2026
    Review
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  7. Article
  8. Review
  9. Article
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  12. Article
  13. Oxidation state-specific fluorescent copper sensors reveal oncogene-driven redox changes that regulate labile copper(II) pools.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  14. Review
  15. The Crossroads between Host Copper Metabolism and Influenza Infection.International journal of molecular sciences · 2021
    Review
  16. 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

6 authors at 2 institutions in 2 countries.

Ekaterina Y IlyechovaLaboratory of Trace elements metabolism, ITMO University, Kronverksky av. 49, 197101 St.-Petersburg, Russia. ikaterina2705@yandex.ru.
Elisa BonaldiLaboratory of molecular pharmacology, Istituto di Ricerche Farmacologiche "Mario Negri", IRCCS, Via La Masa 19, 20156 Milan, Italy. eli.bon89@gmail.com.ORCID 0000-0003-1186-398X
Iurii A OrlovLaboratory of Trace elements metabolism, ITMO University, Kronverksky av. 49, 197101 St.-Petersburg, Russia. orlov239@gmail.com.
Ekaterina A SkomorokhovaLaboratory of Trace elements metabolism, ITMO University, Kronverksky av. 49, 197101 St.-Petersburg, Russia. katjaskom@yandex.ru.
Ludmila V PuchkovaLaboratory of Trace elements metabolism, ITMO University, Kronverksky av. 49, 197101 St.-Petersburg, Russia. puchkovalv@yandex.ru.ORCID 0000-0003-0958-2812
Massimo BrogginiLaboratory of Trace elements metabolism, ITMO University, Kronverksky av. 49, 197101 St.-Petersburg, Russia. massimo.broggini@marionegri.it.ORCID 0000-0002-8138-9358
ITMO University · RUMario Negri Institute for Pharmacological Research · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Copper, the highly toxic micronutrient, plays two essential roles: it is a catalytic and structural cofactor for Cu-dependent enzymes, and it acts as a secondary messenger. In the cells, copper is imported by CTR1 (high-affinity copper transporter 1), a transmembrane high-affinity copper importer, and DMT1 (divalent metal transporter). In cytosol, enzyme-specific chaperones receive copper from CTR1 C-terminus and deliver it to their apoenzymes. DMT1 cannot be a donor of catalytic copper because it does not have a cytosol domain which is required for copper transfer to the Cu-chaperons that assist the formation of cuproenzymes. Here, we assume that DMT1 can mediate copper way required for a regulatory copper pool. To verify this hypothesis, we used CRISPR/Cas9 to generate H1299 cell line with

Indexed as

Carcinoma, Non-Small-Cell LungCation Transport ProteinsCell Line, TumorCell SurvivalCopperCopper Transporter 1CRISPR-Cas SystemsGene Expression Regulation, NeoplasticHumansIon TransportLung NeoplasmsTranscription FactorsCation Transport ProteinsCopperCopper Transporter 1DMRT1 proteinSLC31A1 protein, humanTranscription Factorscisplatincopper homeodynamicscopper importers CTR1 and DMT1CRISPR-Cas9cuproenzymessignalingsilver

Identifiers

PMID30959888
PMCPMC6523758
OpenAlexW2900670401

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.