Evidence map›Paper›PMID 12200695›Full record

ArticleLeukemia2002

HERG potassium channels are constitutively expressed in primary human acute myeloid leukemias and regulate cell proliferation of normal and leukemic hemopoietic progenitors.

S Pillozzi, M F Brizzi, M Balzi, O Crociani, A Cherubini, L Guasti, B Bartolozzi, A Becchetti, E Wanke, P A Bernabei and 3 more

Abstract read
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Article in Leukemia, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

90 citing papers in PubMed, 194 citations in OpenAlex.

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  13. Ion Channel Involvement in Tumor Drug Resistance.Journal of personalized medicine · 2022
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  14. Targeting Ion Channels for Cancer Treatment: Current Progress and Future Challenges.Reviews of physiology, biochemistry and pharmacology · 2022
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  15. Review
  16. Influence of Kv11.1 (hERG1) KPflugers Archiv : European journal of physiology · 2021
    Article
  17. Review
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  19. Antibodies Targeting KBioelectricity · 2019
    Article
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30 more citing papers are in PubMed but not listed here.

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

13 authors at 4 institutions in 1 country.

S PillozziDepartment of Experimental Pathology and Oncology, University of Firenze, Firenze, Italy.
M F Brizzi
M Balzi
O Crociani
A Cherubini
L Guasti
B Bartolozzi
A Becchetti
E Wanke
P A Bernabei
M Olivotto
L Pegoraro
A Arcangeli
University of Florence · ITAzienda Ospedaliero-Universitaria Careggi · ITUniversity of Milano-Bicocca · ITUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An important target in the understanding of the pathogenesis of acute myeloid leukemias (AML) relies on deciphering the molecular features of normal and leukemic hemopoietic progenitors. In particular, the analysis of the mechanisms involved in the regulation of cell proliferation is decisive for the establishment of new targeted therapies. To gain further insight into this topic we report herein a novel approach by analyzing the role of HERG K(+) channels in the regulation of hemopoietic cell proliferation. These channels, encoded by the human ether-a-gò-gò-related gene (herg), belong to a family of K(+) channels, whose role in oncogenesis has been recently demonstrated. We report here that herg is switched off in normal peripheral blood mononuclear cells (PBMNC) as well as in circulating CD34(+) cells, however, it is rapidly turned on in the latter upon induction of the mitotic cycle. Moreover, hergappears to be constitutively activated in leukemic cell lines as well as in the majority of circulating blasts from primary AML. Evidence is also provided that HERG channel activity regulates cell proliferation in stimulated CD34(+) as well as in blast cells from AML patients. These results open new perspectives on the pathogenetic role of HERG K(+) channels in leukemias.

Indexed as

Cation Transport ProteinsDNA-Binding ProteinsPotassium Channels, Voltage-GatedTrans-ActivatorsAcute DiseaseAntigens, CD34BenzenesulfonamidesBenzimidazolesCell DivisionERG1 Potassium ChannelEther-A-Go-Go Potassium ChannelsHematopoietic Stem CellsHumansImmunoenzyme TechniquesLeukemia, MyeloidPatch-Clamp TechniquesAntigens, CD34BenzenesulfonamidesBenzimidazolesCation Transport ProteinsDNA-Binding ProteinsERG1 Potassium ChannelERG protein, humanEther-A-Go-Go Potassium ChannelsKCNH2 protein, humanKCNH6 protein, humanPotassium Channel BlockersPotassium ChannelsPotassium Channels, Voltage-GatedSulfanilamidesTrans-ActivatorsTranscriptional Regulator ERGWAY 123398

Identifiers

PMID12200695
OpenAlexW2040153309

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.