Evidence map›Paper›PMID 25124685›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2014

Clinical implications of phosphorylated STAT3 expression in De Novo diffuse large B-cell lymphoma.

Chi Young Ok, Jiayu Chen, Zijun Y Xu-Monette, Alexandar Tzankov, Ganiraju C Manyam, Ling Li, Carlo Visco, Santiago Montes-Moreno, Karen Dybkær, April Chiu and 18 more

Abstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
–field-weighted citation impact
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

42 citing papers in PubMed.

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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

28 authors.

Chi Young OkDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Jiayu ChenMedical School of Taizhou University, Taizhou, Zhejiang, China.
Zijun Y Xu-MonetteDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Alexandar TzankovUniversity Hospital, Basel, Switzerland.
Ganiraju C ManyamDepartment of Biostatistics and Bioinformatics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Ling LiDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Carlo ViscoSan Bartolo Hospital, Vicenza, Italy.
Santiago Montes-MorenoHospital Universitario Marques de Valdecilla, Santander, Spain.
Karen DybkærAalborg University Hospital, Aalborg, Denmark.
April ChiuMemorial Sloan-Kettering Cancer Center, New York, New York.
Attilio OraziWeill Medical College of Cornell University, New York, New York.
Youli ZuHouston Methodist Hospital, Houston, Texas.
Govind BhagatColumbia University Medical Center and New York Presbyterian Hospital, New York, New York.
Kristy L RichardsUniversity of North Carolina School of Medicine, Chapel Hill, North Carolina.
Eric D HsiCleveland Clinic, Cleveland, Ohio.
William W L ChoiUniversity of Hong Kong Li Ka Shing Faculty of Medicine, Hong Kong, China.
J Han van KriekenRadboud University Nijmegen Medical Centre, Nijmegen, the Netherlands.
Jooryung HuhAsan Medical Center, Ulsan University College of Medicine, Seoul, Korea.
Xiaoying ZhaoZhejiang University School of Medicine, Second University Hospital, Hangzhou, China.
Maurilio PonzoniSan Raffaele H. Scientific Institute, Milan, Italy.
Andrés J M FerreriSan Raffaele H. Scientific Institute, Milan, Italy.
Francesco BertoniIOR Institute of Oncology Research and IOSI Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
John P FarnenGundersen Lutheran Health System, La Crosse, Wisconsin.
Michael B MøllerOdense University Hospital, Odense, Denmark.
Miguel A PirisHospital Universitario Marques de Valdecilla, Santander, Spain.
Jane N WinterFeinberg School of Medicine, Northwestern University, Chicago, Illinois.
L Jeffrey MedeirosDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Ken H YoungDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas. khyoung@mdanderson.org.

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
P4 -TARGETING MULTIPLE MYELOMA BY COMBINING CDK INHIBITORS AND BCL-2 ANTAGONISTSP50CA142509 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KWAK, LARRY W · 2010 to 2014
$11.1M
Convergence of MicroRNAs and p53 Signaling in Multiple Myeloma: Environmental CoR01CA138688 · NCI · UNIVERSITY OF LOUISVILLE · PI LI, YONG · 2009 to 2017
$2.9M
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
Deep Sequencing of Small Regulatory RNAs in Diffuse Large B cell LymphomaRC1CA146299 · NCI · SCRIPPS RESEARCH INSTITUTE, THE · PI XIAO, CHANGCHUN · 2009 to 2010
$1000k
NCI NIH HHS 1RC1CA146299NCI NIH HHS CA016672NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA136411NCI NIH HHS P50CA136411NCI NIH HHS P50 CA142509NCI NIH HHS P50CA142509NCI NIH HHS R01 CA138688NCI NIH HHS R01CA138688NCI NIH HHS RC1 CA146299
6 · The paper itself

Abstract

purposeActivated signal transducer and activator of transcription 3 (STAT3) regulates tumor growth, invasion, cell proliferation, angiogenesis, immune response, and survival. Data regarding expression of phosphorylated (activated) STAT3 in diffuse large B-cell lymphoma (DLBCL) and the impact of phosphorylated STAT3 (pSTAT3) on prognosis are limited. EXPERIMENTAL

designWe evaluated expression of pSTAT3 in de novo DLBCL using immunohistochemistry, gene expression profiling (GEP), and gene set enrichment analysis (GSEA). Results were analyzed in correlation with cell-of-origin (COO), critical lymphoma biomarkers, and genetic translocations.

resultspSTAT3 expression was observed in 16% of DLBCL and was associated with advanced stage, multiple extranodal sites of involvement, activated B-cell-like (ABC) subtype, MYC expression, and MYC/BCL2 expression. Expression of pSTAT3 predicted inferior overall survival (OS) and progression-free survival (PFS) in patients with de novo DLBCL. When DLBCL cases were stratified according to COO or MYC expression, pSTAT3 expression did not predict inferior outcome, respectively. Multivariate analysis showed that the prognostic predictability of pSTAT3 expression was due to its association with the ABC subtype, MYC expression, and adverse clinical features. GEP demonstrated upregulation of genes, which can potentiate function of STAT3. GSEA showed the JAK-STAT pathway to be enriched in pSTAT3(+) DLBCL.

conclusionsThe results of this study provide a rationale for the ongoing successful clinical trials targeting the JAK-STAT pathway in DLBCL.

Indexed as

AdultAgedAntibodies, Monoclonal, Murine-DerivedAntineoplastic Combined Chemotherapy ProtocolsCohort StudiesCyclin D1CyclophosphamideDoxorubicinFemaleGene ExpressionGenes, bcl-2Genes, mycHumansLymphoma, Large B-Cell, DiffuseMaleMiddle AgedAntibodies, Monoclonal, Murine-DerivedCyclin D1CyclophosphamideDoxorubicinNF-kappa BPrednisoneProto-Oncogene Proteins c-aktR-CHOP protocolRituximabSTAT3 Transcription FactorTumor Suppressor Protein p53Vincristine

Identifiers

PMID25124685
PMCPMC4184926

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.