Evidence map›Paper›PMID 28427156›Full record

ArticleOncotarget2017

The effects of DLEU1 gene expression in Burkitt lymphoma (BL): potential mechanism of chemoimmunotherapy resistance in BL.

Sanghoon Lee, Wen Luo, Tishi Shah, Changhong Yin, Timmy O'Connell, Tae-Hoon Chung, Sherrie L Perkins, Rodney R Miles, Janet Ayello, Erin Morris and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 4% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

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  3. Haematologica · 2024
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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

13 authors at 3 institutions in 2 countries.

Sanghoon LeeDepartments of Pediatrics, New York Medical College, Valhalla, New York, USA.
Wen LuoDepartments of Pediatrics, New York Medical College, Valhalla, New York, USA.
Tishi ShahDepartments of Pediatrics, New York Medical College, Valhalla, New York, USA.
Changhong YinDepartments of Pediatrics, New York Medical College, Valhalla, New York, USA.
Timmy O'ConnellDepartments of Pediatrics, New York Medical College, Valhalla, New York, USA.
Tae-Hoon ChungCancer Science Institute of Singapore, National University of Singapore, Singapore.
Sherrie L PerkinsDepartment of Pathology and ARUP Laboratories, University of Utah, Salt Lake City, Utah, USA.
Rodney R MilesDepartment of Pathology and ARUP Laboratories, University of Utah, Salt Lake City, Utah, USA.
Janet AyelloDepartments of Pediatrics, New York Medical College, Valhalla, New York, USA.
Erin MorrisDepartments of Pediatrics, New York Medical College, Valhalla, New York, USA.
Lauren HarrisonDepartments of Pediatrics, New York Medical College, Valhalla, New York, USA.
Carmella van de VenDepartments of Pediatrics, New York Medical College, Valhalla, New York, USA.
Mitchell S CairoDepartments of Pediatrics, New York Medical College, Valhalla, New York, USA.
New York Medical College · USARUP Laboratories (United States) · USNational University Cancer Institute, Singapore · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Following a multivariant analysis we demonstrated that children and adolescents with Burkitt lymphoma (BL) and a 13q14.3 deletion have a significant decrease in event free survival (EFS) despite identical short intensive multi-agent chemotherapy. However, how this deletion in the 13q14.3 region is associated with a significant decrease in EFS in children and adolescents with BL is largely unknown. The gene Deleted in Lymphocytic Leukemia 1 (DLEU1) is located in the region of 13q14.3. Here, we report that DLEU1 expression is implicated in the regulation of BL programmed cell death, cell proliferation, and expression of apoptotic genes in transcription activator-like effector nuclease (TALEN)s-induced DLEU1 knockdown and DLEU1 overexpressing BL cell lines. Furthermore, NSG mice xenografted with DLEU1 knockdown BL cells had significantly shortened survival (p < 0.05 and p < 0.005), whereas those xenografted with DLEU1 overexpressing BL cells had significantly improved survival (p < 0.05 and p < 0.0001), following treatment with rituximab and/or cyclophosphamide. These data suggest that DLEU1 may in part function as a tumor suppressor gene and confer chemoimmunotherapy resistance in children and adolescents with BL.

Indexed as

Chromosome DeletionAdolescentAnimalsAntineoplastic AgentsAntineoplastic Agents, ImmunologicalApoptosisBurkitt LymphomaCell Line, TumorCell ProliferationChildChromosomes, Human, Pair 13CyclophosphamideDisease-Free SurvivalDrug Resistance, NeoplasmFemaleGene Knockdown TechniquesAntineoplastic AgentsAntineoplastic Agents, ImmunologicalCyclophosphamideDLEU1 lncRNA, humanRituximabRNA, Long NoncodingTranscription Activator-Like Effector NucleasesTumor Suppressor ProteinsB-NHLchemoimmunotherapyDLEU1genome editingtumor suppressor

Identifiers

PMID28427156
PMCPMC5438612
OpenAlexW2591514617

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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.