Evidence map›Paper›PMID 25704881›Full record

ArticleOncotarget2015

Dysregulated CXCR4 expression promotes lymphoma cell survival and independently predicts disease progression in germinal center B-cell-like diffuse large B-cell lymphoma.

Jiayu Chen, Zijun Y Xu-Monette, Lijuan Deng, Qi Shen, Ganiraju C Manyam, Azahara Martinez-Lopez, Li Zhang, Santiago Montes-Moreno, Carlo Visco, Alexandar Tzankov and 20 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 6% 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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 80 citations in OpenAlex.

  1. Pooled it
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  6. Exploring G Protein-Coupled Receptors in Hematological Cancers.ACS pharmacology & translational science · 2024
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  10. Role of Fyn in hematological malignancies.Journal of cancer research and clinical oncology · 2023
    Review
  11. GPCR Inhibition in Treating Lymphoma.ACS medicinal chemistry letters · 2022
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
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

30 authors at 20 institutions in 9 countries.

Jiayu ChenMedical School of Taizhou University, Taizhou, Zhejiang, China.
Zijun Y Xu-MonetteDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Lijuan DengDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Qi ShenDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Ganiraju C ManyamDepartment of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Azahara Martinez-LopezHospital Universitario Marques de Valdecilla, Santander, Spain.
Li ZhangDepartment of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Santiago Montes-MorenoHospital Universitario Marques de Valdecilla, Santander, Spain.
Carlo ViscoSan Bortolo Hospital, Vicenza, Italy.
Alexandar TzankovUniversity Hospital, Basel, Switzerland.
Lihui YinDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Karen DybkaerAalborg University Hospital, Aalborg, Denmark.
April ChiuMemorial Sloan-Kettering Cancer Center, New York, NY, USA.
Attilio OraziWeill Medical College of Cornell University, New York, NY, USA.
Youli ZuThe Methodist Hospital, Houston, TX, USA.
Govind BhagatColumbia University Medical Center and New York Presbyterian Hospital, New York, NY, USA.
Kristy L RichardsUniversity of North Carolina School of Medicine, Chapel Hill, NC, USA.
Eric D HsiCleveland Clinic, Cleveland, OH, USA.
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, Netherlands.
Jooryung HuhAsan Medical Center, Ulsan University College of Medicine, Seoul, Korea.
Maurilio PonzoniSan Raffaele H. Scientific Institute, Milan, Italy.
Andrés J M FerreriSan Raffaele H. Scientific Institute, Milan, Italy.
Xiaoying ZhaoZhejiang University School of Medicine, Second University Hospital, Hangzhou, China.
Michael B MøllerOdense University Hospital, Odense, Denmark.
John P FarnenGundersen Lutheran Health System, La Crosse, WI, USA.
Jane N WinterFeinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Miguel A PirisHospital Universitario Marques de Valdecilla, Santander, Spain.
Lan PhamDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Ken H YoungDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
The University of Texas MD Anderson Cancer Center · USMarqués de Valdecilla University Hospital · ESSan Raffaele University of Rome · ITAalborg University Hospital · DKAsan Medical Center · KRCleveland Clinic · USCornell University · USGundersen Health System · USMemorial Sloan Kettering Cancer Center · USMethodist Hospital · USNewYork–Presbyterian Hospital · USNorthwestern University · USOdense University Hospital · DKOspedale San Bortolo · ITRadboud University Medical Center · NLSecond Affiliated Hospital of Zhejiang University · CNTaizhou University · CNUniversity Hospital of Basel · CHUniversity of Hong Kong · HKUniversity of North Carolina at Chapel Hill · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
Convergence of MicroRNAs and p53 Signaling in Multiple Myeloma: Environmental CoR01CA138688 · NCI · UNIVERSITY OF LOUISVILLE · PI LI, YONG · 2009 to 2017
$2.9M
MYC as a Biomarker in Aggressive Non-Hodgkin LymphomaR01CA187415 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI LI, YONG · 2015 to 2019
$2.2M
NCI NIH HHS P30 CA060553NCI NIH HHS R01 CA138688NCI NIH HHS R01CA138688NCI NIH HHS R01 CA187415NCI NIH HHS R01CA187415
6 · The paper itself

Abstract

Abnormal expression of the chemokine receptor CXCR4 plays an essential role in tumor cell dissemination and disease progression. However, the significance of CXCR4 overexpression in de novo diffuse large B cell lymphoma (DLBCL) is unknown. In 743 patients with de novo diffuse large B cell lymphoma (DLBCL) who received standard Rituximab-CHOP immunochemotherapy, we assessed the expression of CXCR4 and dissected its prognostic significance in various DLBCL subsets. Our results showed that CXCR4+ patients was associated with male, bulky tumor, high Ki-67 index, activated B-cell-like (ABC) subtype, and Myc, Bcl-2 or p53 overexpression. Moreover, CXCR4+ was an independent factor predicting poorer progression-free survival in germinal-center B-cell-like (GCB)-DLBCL, but not in ABC-DLBCL; and in patients with an IPI of ≤2, but not in those with an IPI>2. The lack of prognostic significance of CXCR4 in ABC-DLBCL was likely due to the activation of p53 tumor suppressor attenuating CXCR4 signaling. Furthermore, concurrent CXCR4+ and BCL2 translocation showed dismal outcomes resembling but independent of MYC/BCL2 double-hit DLBCL. Gene expression profiling suggested that alterations in the tumor microenvironment and immune responses, increased tumor proliferation and survival, and the dissemination of CXCR4+ tumor cells to distant organs or tissues were underlying molecular mechanisms responsible for the CXCR4+ associated poor prognosis.

Indexed as

Antibodies, Monoclonal, Murine-DerivedAntineoplastic Combined Chemotherapy ProtocolsCell Line, TumorCell ProliferationCell SurvivalChemokine CXCL12CyclophosphamideDisease ProgressionDoxorubicinFemaleGene Expression Regulation, NeoplasticGerminal CenterHumansLymphoma, Large B-Cell, DiffuseMaleMiddle AgedAntibodies, Monoclonal, Murine-DerivedBKT140Chemokine CXCL12CXCL12 protein, humanCXCR4 protein, humanCyclophosphamideDoxorubicinOligopeptidesPrednisoneR-CHOP protocolReceptors, CXCR4RituximabTP53 protein, humanTumor Suppressor Protein p53VincristineBCL2CXCR4DLBCLMycTP53 mutation

Identifiers

PMID25704881
PMCPMC4467389
OpenAlexW1949227380

What OpenQuestion holds

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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.