Evidence map›Paper›PMID 24681958›Full record

ArticleOncogene2015

High-resolution chromatin immunoprecipitation (ChIP) sequencing reveals novel binding targets and prognostic role for SOX11 in mantle cell lymphoma.

P-Y Kuo, V V Leshchenko, M J Fazzari, D Perumal, T Gellen, T He, J Iqbal, S Baumgartner-Wennerholm, L Nygren, F Zhang and 13 more

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
5.1field-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

40 citing papers in PubMed, 64 citations in OpenAlex.

  1. Trial
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  10. Endotype reversal as a novel strategy for screening drugs targeting familial Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2022
    Article
  11. Article
  12. Article
  13. SOX11 Inhibitors Are Cytotoxic in Mantle Cell Lymphoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Article
  14. Article
  15. Highly sensitive and specificHaematologica · 2020
    Article
  16. Article
  17. Sox11 promotes head and neck cancer progression via the regulation of SDCCAG8.Journal of experimental & clinical cancer research : CR · 2019
    Article
  18. Article
  19. SOX11: friend or foe in tumor prevention and carcinogenesis?Therapeutic advances in medical oncology · 2019
    Review
  20. Roles and regulation of SOX transcription factors in skeletogenesis.Current topics in developmental biology · 2019
    Review
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

23 authors at 8 institutions in 3 countries.

P-Y KuoDivision of Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID 0000000311419790
V V LeshchenkoDivision of Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
M J Fazzari1] Department of Population Health, Albert Einstein College of Medicine of Yeshiva University, Bronx, NY, USA [2] Department of Genetics, Albert Einstein College of Medicine of Yeshiva  University, Bronx, NY, USA.
D PerumalDivision of Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
T GellenAlbert Einstein Cancer Center, Albert Einstein College of Medicine of Yeshiva University, Bronx, NY, USA.
T HeDivision of Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
J IqbalDepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, USA.
S Baumgartner-WennerholmDepartment of Medicine, Center for Haematology, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden.
L NygrenDepartment of Laboratory Medicine, Division of Pathology, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden.
F ZhangBioinformatics Laboratory, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
W ZhangBioinformatics Laboratory, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
K S SuhGenomics and Biomarkers Program, John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, NJ, USA.
A GoyGenomics and Biomarkers Program, John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, NJ, USA.
D T YangDepartment of Pathology, School of Medicine and Public Health, University of Wisconsin, Madison, WI, USA.
W-C ChanDepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, USA.
B S KahlDepartment of Medicine, School of Medicine and Public Health, and The UW Carbone Cancer Center, University of Wisconsin, Madison, WI, USA.
A K VermaAlbert Einstein Cancer Center, Albert Einstein College of Medicine of Yeshiva University, Bronx, NY, USA.
R D GascoyneDepartment of Pathology and Experimental Therapeutics, British Columbia Cancer Agency, Vancouver, British Columbia, Canada.
E KimbyDepartment of Medicine, Center for Haematology, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden.
B SanderDepartment of Laboratory Medicine, Division of Pathology, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden.
B H YeDepartment of Cell Biology, Albert Einstein College of Medicine of Yeshiva University, Bronx, NY, USA.
A M Melnick1] Hematology and Oncology Division, Weill Cornell Medical College, New York, NY, USA [2] Department of Pharmacology, Weill Cornell Medical College, New York, NY, USA.
S ParekhDivision of Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Icahn School of Medicine at Mount Sinai · USAlbert Einstein College of Medicine · USKarolinska University Hospital · SEHackensack University Medical Center · USUniversity of Nebraska Medical Center · USUniversity of Wisconsin–Madison · USBC Cancer Agency · CACornell University · US

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI AMY TRENTHAM-DIETZ · 1985 to 2026
$142.6M
WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI THOMAS E ROHAN · 1985 to 2026
$111.2M
Institutional Clinical and Translational Science AwardUL1TR000427 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2012 to 2016
$32.2M
INSTITUTIONAL CTSA (UW-MADISON): CLINICAL TRIALSUL1RR025011 · NCRR · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2007 to 2011
$29.5M
Paul Calabresis Career Development Award For Clinical Oncology K12CA132783 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI PEREZ-SOLER, ROMAN, VERMA, AMIT K. · 2009 to 2019
$8.2M
NCATS NIH HHS 9U54TR000021NCATS NIH HHS UL1 TR000427NCI NIH HHS K12 CA132783NCI NIH HHS K12-CA132783-01NCI NIH HHS P30 CA013330NCI NIH HHS P30 CA014520NCRR NIH HHS 1UL1RR025011NCRR NIH HHS UL1 RR025011
6 · The paper itself

Abstract

Sex determining region Y-box 11 (SOX11) expression is specific for mantle cell lymphoma (MCL) as compared with other non-Hodgkin's lymphomas. However, the function and direct-binding targets of SOX11 in MCL are largely unknown. We used high-resolution chromatin immunoprecipitation sequencing to identify the direct target genes of SOX11 in a genome-wide, unbiased manner and elucidate its functional significance. Pathway analysis identified WNT, PKA and TGF-beta signaling pathways as significantly enriched by SOX11-target genes. Quantitative chromatin immunoprecipitation sequencing and promoter reporter assays confirmed that SOX11 directly binds to individual genes and modulates their transcription activities in these pathways in MCL. Functional studies using RNA interference demonstrate that SOX11 directly regulates WNT in MCL. We analyzed SOX11 expression in three independent well-annotated tissue microarrays from the University of Wisconsin (UW), Karolinska Institute and British Columbia Cancer Agency. Our findings suggest that high SOX11 expression is associated with improved survival in a subset of MCL patients, particularly those treated with intensive chemotherapy. Transcriptional regulation of WNT and other biological pathways affected by SOX11-target genes may help explain the impact of SOX11 expression on patient outcomes.

Indexed as

Antineoplastic Combined Chemotherapy Protocolsbeta CateninBinding SitesCell Cycle CheckpointsCell Line, TumorCell ProliferationCell SurvivalChromatin ImmunoprecipitationGene ExpressionGene Expression Regulation, NeoplasticHigh-Throughput Nucleotide SequencingHumansLymphoma, Mantle-CellNucleotide MotifsPrognosisProtein Bindingbeta CateninSOX11 protein, humanSOXC Transcription FactorsWnt Proteins

Identifiers

PMID24681958
PMCPMC4511176
OpenAlexW1989625297

What OpenQuestion holds

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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.