Evidence map›Paper›PMID 30930624›Full record

ArticleTurkish journal of biology = Turk biyoloji dergisi2018

Long noncoding RNA PVT1: potential oncogene in the development of acute lymphoblastic leukemia.

Narjes Yazdi, Mohammad Houshmand, Amir Atashi, Alireza Kazemi, Ali Anjam Najmedini, Mahin Nikougoftar Zarif

Open access · bronzeAbstract read
In one paragraph

Article in Turkish journal of biology = Turk biyoloji dergisi, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
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  7. lncRNA PVT1: a novel oncogene in multiple cancers.Cellular & molecular biology letters · 2022
    Review
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  15. Editorial: PVT1 in Cancer.Frontiers in oncology · 2020
    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

6 authors at 4 institutions in 1 country.

Narjes YazdiDepartment of Molecular Genetics, Tehran Medical Branch, Islamic Azad University , Tehran , Iran.ORCID https://orcid.org/0000-0001-5956-4589
Mohammad HoushmandBlood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine , Tehran , Iran.ORCID https://orcid.org/0000-0001-7503-6452
Amir AtashiStem Cell and Tissue Engineering Research Center, Shahroud University of Medical Sciences , Shahroud , Iran.ORCID https://orcid.org/0000-0002-3889-5642
Alireza KazemiDepartment of Hematology and Blood Banking, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences , Tehran , Iran.ORCID https://orcid.org/0000-0002-5968-7260
Ali Anjam NajmediniDepartment of Hematology and Blood Banking, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences , Tehran , Iran.ORCID https://orcid.org/0000-0002-0062-0125
Mahin Nikougoftar ZarifBlood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine , Tehran , Iran.ORCID https://orcid.org/0000-0001-5412-5106
High Institute for Education and Research in Transfusion Medicine · IRShahid Beheshti University of Medical Sciences · IRIslamic Azad University Medical Branch of Tehran · IRShahroud University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emerging evidence shows that long noncoding RNAs (lncRNAs) participate in various cellular processes, and that plasmacytoma variant translocation 1 (PVT1), a newly described oncogene that interacts with various molecules such as p15, p16, NOP2, and c-Myc, is a major contributing factor in tumor development. However, the role of this oncogene remains unknown in the pathogenesis of acute lymphoblastic leukemia (ALL), the most prevalent form of childhood leukemia. In this study, we first measure the expression level of PVT1 in a Jurkat cell line, then small interfering (siRNA) PVT1 is applied to demonstrate the impact of PVT1 knockdown in apoptosis, proliferation, the cell cycle, and its downstream targets. Our findings show that lncRNA was significantly higher in the ALL cell line than normal lymphocytes and that PVT1 knock-down increased the rate of apoptosis, caused G0/G1 arrest in the cell cycle, reduced the proliferation rate, and, above all, reduced the stability of c-Myc protein. All findings were confirmed at the molecular level. Our results may indicate the role of PVT1 knock-down in the suppression of ALL development and might provide an option for targeted therapy for leukemic conditions.

Indexed as

acute lymphoblastic leukemiac-MycLong noncoding RNAPVT1siRNA

Identifiers

PMID30930624
PMCPMC6438125
OpenAlexW2898389924

What OpenQuestion holds

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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.