Evidence map›Paper›PMID 28801451›Full record

ArticleBlood2017

Adult high-grade B-cell lymphoma with Burkitt lymphoma signature: genomic features and potential therapeutic targets.

Alyssa Bouska, Chengfeng Bi, Waseem Lone, Weiwei Zhang, Ambreen Kedwaii, Tayla Heavican, Cynthia M Lachel, Jiayu Yu, Roberto Ferro, Nanees Eldorghamy and 22 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
10.2field-weighted citation impact, top 1% 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

41 citing papers in PubMed, 83 citations in OpenAlex.

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  18. Genetic mechanism for the loss of PRAME in B cell lymphomas.The Journal of clinical investigation · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

32 authors at 15 institutions in 4 countries.

Alyssa BouskaPathology and Microbiology and.
Chengfeng BiPathology and Microbiology and.
Waseem LonePathology and Microbiology and.
Weiwei ZhangPathology and Microbiology and.
Ambreen KedwaiiPathology and Microbiology and.
Tayla HeavicanPathology and Microbiology and.
Cynthia M LachelDivision of Hematology and Oncology, University of Nebraska Medical Center, Omaha, NE.
Jiayu YuPathology and Microbiology and.
Roberto FerroDivision of Hematology and Oncology, University of Nebraska Medical Center, Omaha, NE.
Nanees EldorghamyPathology and Microbiology and.
Timothy C GreinerPathology and Microbiology and.
Julie VoseDivision of Hematology and Oncology, University of Nebraska Medical Center, Omaha, NE.
Dennis D WeisenburgerDepartment of Pathology, City of Hope National Medical Center, Duarte, CA.
Randy D GascoyneCenter for Lymphoid Cancer, British Columbia Cancer Agency, Vancouver, BC, Canada.
Andreas RosenwaldDepartment of Pathology, University of Würzburg and Comprehensive Cancer Center Mainfranken, Würzburg, Germany.
German OttDepartment of Clinical Pathology, Robert-Bosch-Krankenhaus, and Dr. Margarete Fischer-Bosch Institute of Clinical Pharmacology, Stuttgart, Germany.
Elias CampoHematopathology Unit, Hospital Clinic, Barcelona, Spain.
Lisa M RimszaDepartment of Pathology, University of Arizona, Tucson, AZ.
Elaine S JaffeLaboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health (NIH), Bethesda, MD.
Rita M BrazielOregon Health Sciences Center, Portland, OR.
Reiner SiebertInstitute of Human Genetics, University Hospital of Ulm, Ulm, Germany.
Rodney R MilesDepartment of Pathology, University of Utah Health Sciences Center, Salt Lake City, UT.
Sandeep DaveInstitute of Genome Sciences and Department of Medicine, Duke University Medical Center, Durham, NC.
Anupama ReddyInstitute of Genome Sciences and Department of Medicine, Duke University Medical Center, Durham, NC.
Jan DelabieDepartment of Pathology, University of Toronto, Toronto, ON, Canada.
Louis M StaudtMetabolism Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD.
Joo Y SongDepartment of Pathology, City of Hope National Medical Center, Duarte, CA.
Timothy W McKeithanDepartment of Pathology, City of Hope National Medical Center, Duarte, CA.
Kai FuPathology and Microbiology and.
Michael GreenEppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, NE; and.
Wing C ChanDepartment of Pathology, City of Hope National Medical Center, Duarte, CA.
Javeed IqbalPathology and Microbiology and.
City Of Hope National Medical Center · USUniversity of Nebraska Medical Center · USBC Cancer Agency · CACenter for Cancer Research · USDr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology · DEDuke Medical Center · USDuke University Hospital · USHospital Clínic de Barcelona · ESNational Institutes of Health · USOregon Health & Science University · USUniversity Hospital Ulm · DEUniversity of Arizona · USUniversity of Toronto · CAUniversity of Utah · USUniversity of Würzburg · DE

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI STANLEY R. HAMILTON · 1985 to 2026
$86.3M
UNMC/EPPLEY CANCER CENTER SUPPORT GRANTP30CA036727 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Apar Kishor Ganti · 1985 to 2026
$55.0M
Molecular diagnosis and outcome prediction in lymphomaZIABC011006 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI STAUDT, LOUIS · 2009 to 2025
$21.0M
Molecular Diagnosis and Prognosis in Aggressive LymphomaU01CA157581 · NCI · UNIVERSITY OF ARIZONA · PI RIMSZA, LISA · 2011 to 2015
$3.1M
UT M.D. Anderson Cancer Center Lymphoma SPOREP50CA136411 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KWAK, LARRY W · 2009 to 2011
$1.5M
NCI NIH HHS P30 CA033572NCI NIH HHS P30 CA036727NCI NIH HHS P50 CA136411NCI NIH HHS U01 CA157581
6 · The paper itself

Abstract

The adult high-grade B-cell lymphomas sharing molecular features with Burkitt lymphoma (BL) are highly aggressive lymphomas with poor clinical outcome. High-resolution structural and functional genomic analysis of adult Burkitt lymphoma (BL) and high-grade B-cell lymphoma with BL gene signature (adult-molecularly defined BL [mBL]) revealed the MYC-ARF-p53 axis as the primary deregulated pathway. Adult-mBL had either unique or more frequent genomic aberrations (del13q14, del17p, gain8q24, and gain18q21) compared with pediatric-mBL, but shared commonly mutated genes. Mutations in genes promoting the tonic B-cell receptor (BCR)→PI3K pathway (

Indexed as

Gene Expression Regulation, NeoplasticTranscriptomeAdolescentAdultAgedAged, 80 and overB-LymphocytesBurkitt LymphomaCell Line, TumorChildChild, PreschoolFemaleHumansImmunophenotypingLymphoma, B-CellMale

Identifiers

PMID28801451
PMCPMC5649549
OpenAlexW2743064314

What OpenQuestion holds

Textmetadata
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.