Evidence map›Paper›PMID 32300452›Full record

ArticleJournal of hematology2019

Changes in

Jayse Alves, Georgia Muccillo Dexheimer, Laura Reckzigel, Marcia Goettert, Vanderlei Biolchi, Ana Lucia Abujamra

Open access · greenAbstract read
In one paragraph

Article in Journal of hematology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 85% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
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 1 institution in 1 country.

Jayse AlvesGraduate Program in Biotechnology, Univates, Lajeado, R.S., 95914-014, Brazil.
Georgia Muccillo DexheimerGraduate Program in Biotechnology, Univates, Lajeado, R.S., 95914-014, Brazil.
Laura ReckzigelBiological and Health Sciences Center, Univates, Lajeado, R.S., 95914-014, Brazil.
Marcia GoettertGraduate Program in Biotechnology, Univates, Lajeado, R.S., 95914-014, Brazil.
Vanderlei BiolchiBiological and Health Sciences Center, Univates, Lajeado, R.S., 95914-014, Brazil.
Ana Lucia AbujamraGraduate Program in Biotechnology, Univates, Lajeado, R.S., 95914-014, Brazil.
Univates · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHematological malignancies are a heterogeneous group of tumors with increased proliferative and auto-replicative capacity. Despite treatment advances, post-treatment quality of life remains highly affected. Studies addressing the molecular mechanisms of these diseases are critical for the development of effective, rapid and selective therapies, since few therapeutic strategies succeed in being effective without triggering high-grade toxicities or debilitating late effects. Our aim of this study was to verify changes in the expression of genes involved in the malignant phenotype of hematological malignancies, by treating human cell lines

methodsKASUMI-1 and K-562 human myeloid leukemia cell lines were plated at a density of 3 × 10

resultsA modulation in gene expression was observed before and after treatment with classic chemotherapeutic agents. It was possible to demonstrate a difference in gene expression when cells were treated with chemotherapeutic agents or decitabine alone when compared to chemotherapeutic agents in association with decitabine.

conclusionsThe genes tested, and the modulation of their expression during

Indexed as

ChemotherapyDecitabineGene expression biomarkersMyeloid leukemia

Identifiers

PMID32300452
PMCPMC7153660
OpenAlexW2978042162

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.