Evidence map›Paper›PMID 31519943›Full record

ArticleScientific reports2019

ALKBH overexpression in head and neck cancer: potential target for novel anticancer therapy.

Tomaš Pilžys, Michał Marcinkowski, Wojciech Kukwa, Damian Garbicz, Małgorzata Dylewska, Karolina Ferenc, Adam Mieczkowski, Andrzej Kukwa, Ewa Migacz, Dominika Wołosz and 5 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

44 citing papers in PubMed, 68 citations in OpenAlex.

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  13. The Molecular Basis of Human ALKBH3 Mediated RNA NAngewandte Chemie (International ed. in English) · 2024
    Article
  14. Article
  15. m6A modification of mRNA in skin diseases.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2022
    Article
  16. Article
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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

15 authors at 4 institutions in 2 countries.

Tomaš PilžysInstitute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland.
Michał MarcinkowskiInstitute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland.
Wojciech KukwaDepartment of Otolaryngology, Medical University of Warsaw, Warsaw, Poland.
Damian GarbiczInstitute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland.
Małgorzata DylewskaInstitute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland.
Karolina FerencVeterinary Research Centre and Center for Biomedical Research, Department of Large Animal Diseases with the Clinic, Faculty of Veterinary Medicine, Warsaw University of Life Sciences, Warsaw, Poland.ORCID http://orcid.org/0000-0002-0100-9328
Adam MieczkowskiInstitute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland.
Andrzej KukwaDepartment of Otolaryngology, Medical University of Warsaw, Warsaw, Poland.
Ewa MigaczDepartment of Otolaryngology, Medical University of Warsaw, Warsaw, Poland.
Dominika WołoszDepartment of Pathology, Medical University of Warsaw, Warsaw, Poland.
Damian MieleckiInstitute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland.
Arne KlunglandDepartment of Microbiology, Oslo University Hospital, Oslo, Norway.
Jan PiwowarskiInstitute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland.
Jarosław PoznańskiInstitute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland. jarek@ibb.waw.pl.ORCID http://orcid.org/0000-0003-2684-1775
Elżbieta GrzesiukInstitute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland. elag@ibb.waw.pl.
Institute of Biochemistry and Biophysics, Polish Academy of Sciences · PLMedical University of Warsaw · PLOslo University Hospital · NOWarsaw University of Life Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The nine identified human homologues of E. coli AlkB 2-oxoglutarate (2OG) and Fe(II)-dependent dioxygenase, ALKBH1-8 and FTO, display different substrate specificities and diverse biological functions. Here we discovered the combined overexpression of members of the ALKBH family in head and neck squamous cell carcinomas (HNSCC). We found direct correlation of ALKBH3 and FTO expression with primary HNSCC tumor size. We observed unidentified thus far cytoplasmic localization of ALKBH2 and 5 in HNSCC, suggesting abnormal role(s) of ALKBH proteins in cancer. Further, high expression of ALKBHs was observed not only in HNSCC, but also in several cancerous cell lines and silencing ALKBH expression in HeLa cancer cells resulted in dramatically decreased survival. Considering the discovered impact of high expression of ALKBH proteins on HNSCC development, we screened for ALKBH blockers among newly synthetized anthraquinone derivatives and demonstrated their potential to support standard anticancer therapy.

Indexed as

AgedAlkB Homolog 3, Alpha-Ketoglutarate-Dependent DioxygenaseAlpha-Ketoglutarate-Dependent Dioxygenase FTOAnthraquinonesBiomarkers, TumorFemaleFollow-Up StudiesHead and Neck NeoplasmsHumansKetoglutaric AcidsMaleMiddle AgedPrognosisSquamous Cell Carcinoma of Head and NeckSubstrate SpecificityTumor Cells, CulturedALKBH3 protein, humanAlkB Homolog 3, Alpha-Ketoglutarate-Dependent DioxygenaseAlpha-Ketoglutarate-Dependent Dioxygenase FTOAnthraquinonesBiomarkers, TumorFTO protein, humanKetoglutaric Acids

Identifiers

PMID31519943
PMCPMC6744417
OpenAlexW2972509213

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.