Evidence map›Paper›PMID 27831553›Full record

ArticleCell death & disease2016

Reed-Sternberg cells in Hodgkin's lymphoma present features of cellular senescence.

J Gopas, E Stern, U Zurgil, J Ozer, A Ben-Ari, G Shubinsky, A Braiman, R Sinay, J Ezratty, V Dronov and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.2field-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

27 citing papers in PubMed, 52 citations in OpenAlex.

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  14. Case report: GermlineFrontiers in oncology · 2024
    Article
  15. Therapy-induced senescent tumor cells in cancer relapse.Journal of the National Cancer Center · 2023
    Review
  16. Article
  17. Review
  18. Review
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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.

J GopasThe Shraga Segal Department of Microbiology Immunology and Genetics, Faculty of Health Sciences, Ben Gurion University of The Negev, Beer Sheva 84105, Israel.
E SternThe Shraga Segal Department of Microbiology Immunology and Genetics, Faculty of Health Sciences, Ben Gurion University of The Negev, Beer Sheva 84105, Israel.
U ZurgilThe Shraga Segal Department of Microbiology Immunology and Genetics, Faculty of Health Sciences, Ben Gurion University of The Negev, Beer Sheva 84105, Israel.
J OzerThe Shraga Segal Department of Microbiology Immunology and Genetics, Faculty of Health Sciences, Ben Gurion University of The Negev, Beer Sheva 84105, Israel.
A Ben-AriThe Shraga Segal Department of Microbiology Immunology and Genetics, Faculty of Health Sciences, Ben Gurion University of The Negev, Beer Sheva 84105, Israel.
G ShubinskyThe Shraga Segal Department of Microbiology Immunology and Genetics, Faculty of Health Sciences, Ben Gurion University of The Negev, Beer Sheva 84105, Israel.
A BraimanThe Shraga Segal Department of Microbiology Immunology and Genetics, Faculty of Health Sciences, Ben Gurion University of The Negev, Beer Sheva 84105, Israel.
R SinayThe Shraga Segal Department of Microbiology Immunology and Genetics, Faculty of Health Sciences, Ben Gurion University of The Negev, Beer Sheva 84105, Israel.
J EzrattyThe Shraga Segal Department of Microbiology Immunology and Genetics, Faculty of Health Sciences, Ben Gurion University of The Negev, Beer Sheva 84105, Israel.
V DronovDepartment of Pathology, Soroka University Medical Center, Beer Sheva 84105, Israel.
S BalachandranBlood Cell Development and Function Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
D BenharrochDepartment of Pathology, Soroka University Medical Center, Beer Sheva 84105, Israel.
E LivnehThe Shraga Segal Department of Microbiology Immunology and Genetics, Faculty of Health Sciences, Ben Gurion University of The Negev, Beer Sheva 84105, Israel.
Ben-Gurion University of the Negev · ILSoroka Medical Center · ILFox Chase Cancer Center · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Margaret von Mehren · 1985 to 2026
$138.8M
NCI NIH HHS P30 CA006927
6 · The paper itself

Abstract

Hodgkin's Lymphoma (HL) is one of the most prevailing malignancies in young adults. Reed-Sternberg (RS) cells in HL have distinctive large cell morphology, are characteristic of the disease and their presence is essential for diagnosis. Enlarged cells are one of the hallmarks of senescence, but whether RS cells are senescent has not been previously investigated. Here we show that RS cells have characteristics of senescent cells; RS cells in HL biopsies specifically express the senescence markers and cell cycle inhibitors p21

Indexed as

Cellular Senescencebeta-GalactosidaseBiomarkers, TumorBiopsyCell Line, TumorCell SizeCytokinesFemaleHodgkin DiseaseHumansImmunohistochemistryInflammation MediatorsMaleMiddle AgedNF-kappa BOxidative Stressbeta-GalactosidaseBiomarkers, TumorCytokinesInflammation MediatorsNF-kappa B

Identifiers

PMID27831553
PMCPMC5287295
OpenAlexW2550461686

What OpenQuestion holds

Textmetadata
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.