Evidence map›Paper›PMID 20023378›Full record

ReviewCell cycle (Georgetown, Tex.)2010

Blocking ovarian cancer progression by targeting tumor microenvironmental leukocytes.

Juan R Cubillos-Ruiz, Melanie Rutkowski, Jose R Conejo-Garcia

Open access · bronzeAbstract readReview
In one paragraph

Review in Cell cycle (Georgetown, Tex.), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

28 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Immunostaining of stromal CD56 cells in ovarian malignancies.Revista da Associacao Medica Brasileira (1992) · 2023
    Article
  3. Review
  4. Inflammation and immunity in ovarian cancer.EJC supplements : EJC : official journal of EORTC, European Organization for Research and Treatment of Cancer ... [et al.] · 2020
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. VEGF Potentiates GD3-Mediated Immunosuppression by Human Ovarian Cancer Cells.Clinical cancer research : an official journal of the American Association for Cancer Research · 2016
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Reprogramming immune responses via microRNA modulation.microRNA diagnostics and therapeutics · 2013
    Article
  18. The immune system in the pathogenesis of ovarian cancer.Critical reviews in immunology · 2013
    Review
  19. Review
  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

3 authors at 1 institution in 1 country.

Juan R Cubillos-RuizDepartments of Microbiology and Immunology, Lebanon, NH, USA.
Melanie Rutkowski
Jose R Conejo-Garcia
Dartmouth Hospital · GB

Funding

THE ROLE OF CAL IN CIF-MEDIATED DEGRADATION OF CFTRP20RR018787 · NCRR · DARTMOUTH COLLEGE · PI O'TOOLE, GEORGE A. · 2003 to 2011
$21.9M
Vascular Leukocytes Influence the Tumor MicroenvironmentR01CA124515 · NCI · WISTAR INSTITUTE · PI Jose R Conejo-Garcia · 2007 to 2026
$7.1M
Boosting anti-tumor immune responses by modulating genes with nanoparticlesR21CA132026 · NCI · WISTAR INSTITUTE · PI CONEJO-GARCIA, JOSE R · 2009 to 2010
$403k
NCI NIH HHS R01 CA124515NCI NIH HHS R01CA124515NCI NIH HHS R01CA124515-S3NCI NIH HHS R21 CA132026NCI NIH HHS R21CA132026NCRR NIH HHS P20 RR018787NCRR NIH HHS P20RR018787NIMHD NIH HHS L60 MD001952
6 · The paper itself

Abstract

Current therapies for metastatic ovarian carcinoma are based on surgical debulking followed by chemotherapy. After more than three decades implementing treatments that selectively target the tumor cell, the 5-year survival rate for metastatic ovarian cancer patients is still lower than 30%. Novel strategies are therefore urgently needed to complement classical treatments for this malignancy. Recently, leukocytes in the ovarian cancer microenvironment such as regulatory T cells and immature pro-angiogenic/tolerogenic myeloid cells have been demonstrated to play a fundamental role in tumor progression. This review focuses on our recent understanding of the potential of eliminating and/or modulating the phenotype of these leukocytes in vivo and in situ as a novel intervention to complement standard ovarian cancer treatments. The significant effects of targeting these crucial microenvironmental players on cancer vascularization, local tumor growth, distal metastatic spreading and spontaneous anti-tumor immune responses are discussed.

Indexed as

ArginaseCarcinomaDendritic CellsDisease ProgressionFemaleHumansIndoleamine-Pyrrole 2,3,-DioxygenaseInterleukin-10LeukocytesOvarian NeoplasmsT-Lymphocytes, RegulatoryTransforming Growth Factor betaArginaseIndoleamine-Pyrrole 2,3,-DioxygenaseInterleukin-10Transforming Growth Factor beta

Identifiers

PMID20023378
PMCPMC3056209
OpenAlexW2044199851

What OpenQuestion holds

Textmetadata
LicenceTDM
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.