Evidence map›Paper›PMID 20415597›Full record

ReviewExpert opinion on biological therapy2010

Inhibiting the inhibitors: evaluating agents targeting cancer immunosuppression.

Theresa L Whiteside

Abstract readReview
In one paragraph

Review in Expert opinion on biological therapy, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.6field-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

38 citing papers in PubMed, 92 citations in OpenAlex.

  1. Observational
  2. CXCR5Nature communications · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Cancer immunoprevention.Current opinion in immunology · 2016
    Review
  14. Article
  15. Clinical Impact of Regulatory T cells (Treg) in Cancer and HIV.Cancer microenvironment : official journal of the International Cancer Microenvironment Society · 2015
    Article
  16. TLR9-Targeted STAT3 Silencing Abrogates Immunosuppressive Activity of Myeloid-Derived Suppressor Cells from Prostate Cancer Patients.Clinical cancer research : an official journal of the American Association for Cancer Research · 2015
    Article
  17. Review
  18. Murine lung cancer induces generalized T-cell exhaustion.The Journal of surgical research · 2015
    Article
  19. Programmed death-1 checkpoint blockade in acute myeloid leukemia.Expert opinion on biological therapy · 2015
    Review
  20. 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

1 author at 1 institution in 1 country.

Theresa L WhitesideUniversity of Pittsburgh Cancer Institute, Hillman Cancer Center, Pathology, 5117 Centre Avenue, Pittsburgh, 15213 USA. whitesidetl@upmc.edu
Weatherford College · US

Funding

Tissue Procurement / ImmunohistologyP01CA109688 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SCHLESSELMAN, JAMES J · 2006 to 2010
$5.9M
Second Primary Tumor Prevention w/EGFR TKIs & COX-2 inhibitors in H & N CancerR01CA112643 · NCI · EMORY UNIVERSITY · PI SHIN, DONG M · 2006 to 2011
$1.6M
NCI NIH HHS P01 CA109688NCI NIH HHS P01-CA109688NCI NIH HHS R01 CA112643NCI NIH HHS R01-CA112643
6 · The paper itself

Abstract

importance of the fieldImmunotherapy of cancer has not improved disease-free or overall patient survival. The lack of concordance between immunological and clinical responses in cancer immunotherapy trials is thought to result from the pervasive presence of tumor-driven immune suppression that allows tumor to escape and that has not been adequately targeted by current therapies. AREAS COVERED IN THIS REVIEW: Because multiple mechanisms of tumor induced suppression have been identified and shown to contribute to tumor escape, the opportunity arises to interfere with these mechanisms. A range of known tumor-derived inhibitors can now be blocked or neutralized by biologic or metabolic agents. Used alone or in combination with each other or with conventional cancer therapies, these agents offer novel therapeutic strategies for the control of tumor escape. WHAT THE READER WILL GAIN: This review deals with currently available inhibitors for counteracting tumor immune escape. The restoration of effective anti-tumor immunity in patients with cancer will require new approaches aiming at: i) protection of immune cells from adverse effects of myeloid-derived suppressor cells, regulatory T cells or inhibitory factors thus enhancing effector functions; and ii) prolonging survival of central memory T cells, thus ensuring long-term protection. TAKE HOME MESSAGE: Inhibitors of mechanisms responsible for tumor escape could restore anti-tumor immune responses in patients with cancer.

Indexed as

AnimalsAntibodies, MonoclonalAntineoplastic AgentsBiological ProductsEnzyme InhibitorsHumansImmunologic MemoryImmunotherapyLymphocytes, Tumor-InfiltratingNeoplasmsT-LymphocytesTreatment OutcomeTumor EscapeAntibodies, MonoclonalAntineoplastic AgentsBiological ProductsEnzyme Inhibitors

Identifiers

PMID20415597
PMCPMC2882984
OpenAlexW2115416471

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.