Evidence map›Paper›PMID 39562620›Full record

ArticleScientific reports2024

A new cancer/testis long noncoding RNA, the OTP-AS1 RNA.

Iuliia K Karnaukhova, Dmitrii E Polev, Larisa L Krukovskaya, Andrei A Makashov, Alexey E Masharsky, Olga V Nazarenko, Irina V Poverennaya, Vsevolod J Makeev, Ekaterina B Akulova, Andrei P Kozlov

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Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

2 citing papers in PubMed.

  1. International journal of molecular sciences · 2023
    Review
  2. The Theory ofGenes · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Iuliia K KarnaukhovaVavilov Institute of General Genetics, Moscow, Russia.
Dmitrii E PolevThe Biomedical Center, St. Petersburg, Russia.
Larisa L KrukovskayaThe Biomedical Center, St. Petersburg, Russia.
Andrei A MakashovPeter the Great St. Petersburg Polytechnic University, St. Petersburg, Russia.
Alexey E MasharskyThe Biomedical Center, St. Petersburg, Russia.
Olga V NazarenkoThe Biomedical Center, St. Petersburg, Russia.
Irina V PoverennayaVavilov Institute of General Genetics, Moscow, Russia.
Vsevolod J MakeevVavilov Institute of General Genetics, Moscow, Russia.
Ekaterina B AkulovaVavilov Institute of General Genetics, Moscow, Russia.
Andrei P KozlovVavilov Institute of General Genetics, Moscow, Russia. contact@biomed.spb.ru.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The orthopedia homeobox (OTP) gene encodes a homeodomain-containing transcription factor involved in brain development. OTP is mapped to human chromosome 5q14.1. Earlier we described transcription in the second intron of this gene in wide variety of tumors, but among normal tissues only in testis. In GeneBank these transcripts are represented by several 300-400 nucleotide long AI267901-like ESTs. We assumed that the AI267901-like ESTs belonged to the longer transcript(s). We used the Rapid Amplification of cDNA Ends (RACE) approach and other methods to find the full-length transcript. The transcript we found was a 2436 nucleotide polyadenylated sequence in antisense to OTP gene. The corresponding gene consisted of two exons separated by an intron of 2961 bp. The first exon was found to be 91 bp long and located in the third exon of OTP. The second exon was 2345 bp long and located in the second intron of OTP. We have shown the expression of this gene in many human tumors but as few as a single sample of normal testis. The transcript lacked significant ORFs suggesting that we discovered a new antisense cancer/testis (CT) sequence OTP-AS1 (OTP-antisense RNA 1), which belongs to the class of long noncoding RNAs (lncRNAs). According to our findings we assume that OTP-AS1 and OTP genes may be a CT-coding gene/CT-ncRNA pair, or sense-antisense gene pair involved in regulatory interactions.

Indexed as

RNA, Long NoncodingTestisExonsGene Expression Regulation, NeoplasticHomeodomain ProteinsHumansMaleRNA, AntisenseTesticular NeoplasmsHomeodomain ProteinsRNA, AntisenseRNA, Long Noncoding

Identifiers

PMID39562620
PMCPMC11576910

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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.