Evidence map›Paper›PMID 22300941›Full record

ArticleJournal of hematology & oncology2012

Deregulation of apoptosis-related genes is associated with PRV1 overexpression and JAK2 V617F allele burden in Essential Thrombocythemia and Myelofibrosis.

Raquel Tognon, Elainy P L Gasparotto, Renata P Neves, Natália S Nunes, Aline F Ferreira, Patrícia V B Palma, Simone Kashima, Dimas T Covas, Mary Santana, Elizabeth X Souto and 4 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in Journal of hematology & oncology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

22 citing papers in PubMed, 50 citations in OpenAlex.

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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

14 authors at 3 institutions in 1 country.

Raquel TognonDepartment of Clinical, Toxicological and Bromatological Analysis, University of São Paulo, Ribeirão Preto, Brazil.
Elainy P L Gasparotto
Renata P Neves
Natália S Nunes
Aline F Ferreira
Patrícia V B Palma
Simone Kashima
Dimas T Covas
Mary Santana
Elizabeth X Souto
Maria Aparecida Zanichelli
Belinda P Simões
Ana Maria de Souza
Fabíola A Castro
Universidade de São Paulo · BRDr. Euryclides Hospital de Jesus Zerbini · BRNational Council for Scientific and Technological Development · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEssential Thrombocythemia (ET) and Primary Myelofibrosis (PMF) are Chronic Myeloproliferative Neoplasms (MPN) characterized by clonal myeloproliferation/myeloaccumulation without cell maturation impairment. The JAK2 V617F mutation and PRV1 gene overexpression may contribute to MPN physiopathology. We hypothesized that deregulation of the apoptotic machinery may also play a role in the pathogenesis of ET and PMF. In this study we evaluated the apoptosis-related gene and protein expression of BCL2 family members in bone marrow CD34+ hematopoietic stem cells (HSC) and peripheral blood leukocytes from ET and PMF patients. We also tested whether the gene expression results were correlated with JAK2 V617F allele burden percentage, PRV1 overexpression, and clinical and laboratory parameters.

resultsBy real time PCR assay, we observed that A1, MCL1, BIK and BID, as well as A1, BCLW and BAK gene expression were increased in ET and PMF CD34+ cells respectively, while pro-apoptotic BAX and anti-apoptotic BCL2 mRNA levels were found to be lower in ET and PMF CD34+ cells respectively, in relation to controls. In patients' leukocytes, we detected an upregulation of anti-apoptotic genes A1, BCL2, BCL-XL and BCLW. In contrast, pro-apoptotic BID and BIMEL expression were downregulated in ET leukocytes. Increased BCL-XL protein expression in PMF leukocytes and decreased BID protein expression in ET leukocytes were observed by Western Blot. In ET leukocytes, we found a correlation between JAK2 V617F allele burden and BAX, BIK and BAD gene expression and between A1, BAX and BIK and PRV1 gene expression. A negative correlation between PRV1 gene expression and platelet count was observed, as well as a positive correlation between PRV1 gene expression and splenomegaly.

conclusionsOur results suggest the participation of intrinsic apoptosis pathway in the MPN physiopathology. In addition, PRV1 and JAK2 V617F allele burden were linked to deregulation of the apoptotic machinery.

Indexed as

ApoptosisAdultAgedAged, 80 and overApoptosis Regulatory Proteinsbcl-2-Associated X Proteinbcl-Associated Death ProteinBlotting, WesternCase-Control StudiesFemaleGPI-Linked ProteinsHumansIsoantigensJanus Kinase 2MaleMembrane ProteinsApoptosis Regulatory ProteinsBAD protein, humanBAX protein, humanbcl-2-Associated X Proteinbcl-Associated Death ProteinBIK protein, humanCD177 protein, humanGPI-Linked ProteinsIsoantigensJAK2 protein, humanJanus Kinase 2Membrane ProteinsMitochondrial ProteinsReceptors, Cell SurfaceRNA, Messenger

Identifiers

PMID22300941
PMCPMC3298534
OpenAlexW2135775813

What OpenQuestion holds

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LicenceCC BY
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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.