Evidence map›Paper›PMID 35538282›Full record

ArticleDoklady. Biochemistry and biophysics2022

5-Azacytidine Suppresses the Expression of Tissue-Specific Oct-1 Isoform in Namalwa Burkitt's Lymphoma Cell Culture.

A P Kotnova, A G Stepchenko, Yu V Ilyin, S G Georgieva, E V Pankratova

Open access · hybridAbstract read
In one paragraph

Article in Doklady. Biochemistry and biophysics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 92% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

5 authors at 1 institution in 1 country.

A P KotnovaEngelhardt Institute of Molecular Biology of Russian Academy of Sciences, Moscow, Russia. alina_kotnova@mail.ru.
A G StepchenkoEngelhardt Institute of Molecular Biology of Russian Academy of Sciences, Moscow, Russia.
Yu V IlyinEngelhardt Institute of Molecular Biology of Russian Academy of Sciences, Moscow, Russia.
S G GeorgievaEngelhardt Institute of Molecular Biology of Russian Academy of Sciences, Moscow, Russia.
E V PankratovaEngelhardt Institute of Molecular Biology of Russian Academy of Sciences, Moscow, Russia.
Engelhardt Institute of Molecular Biology · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overexpression of the transcription factor POU2F1 (Oct-1) increases the malignant potential of the tumor and determines the unfavorable prognosis for both solid and hematological cases of the disease in human carcinogenesis. The Oct-1 level determines the rate of development of the disease in acute myelodysplastic leukemia (AML), and a decrease in its expression significantly delays the development of leukemia in mice; however, a complete knockout of Oct-1 leads to the death of the animals. POU2F1 (Oct-1) is expressed as several isoforms transcribed from alternative promoters. They include both ubiquitous and tissue-specific isoforms. It was shown that in Burkitt's lymphoma Namalwa cells 5-azacytidine specifically suppresses the expression of the tissue-specific isoform Oct-1L mRNA (level of Oct-1L is abnormally increased in these cells), while not causing changes in the amount of the ubiquitous isoform Oct-1A mRNA. These results show that it is possible to selectively reduce the transcription level of the Oct-1L isoform aberrantly expressed in human tumor cells.

Indexed as

AzacitidineBurkitt LymphomaLeukemiaOctamer Transcription Factor-1AnimalsCell Culture TechniquesMiceProtein IsoformsRNA, MessengerTumor Cells, CulturedAzacitidineOctamer Transcription Factor-1Pou2f1 protein, mouseProtein IsoformsRNA, Messenger5-azacytidinealternative promotersBurkitt’s lymphomatranscription factor POU2F1 (Oct-1)

Identifiers

PMID35538282
PMCPMC9090699
OpenAlexW4280490894

What OpenQuestion holds

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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.