Evidence map›Paper›PMID 14685780›Full record

ReviewCancer immunology, immunotherapy : CII2004

Tumour escape: antitumour effectors too much of a good thing?

Graham Pawelec

Open access · greenAbstract readReview
In one paragraph

Review in Cancer immunology, immunotherapy : CII, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
4.9field-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

22 citing papers in PubMed, 87 citations in OpenAlex.

  1. Review
  2. Stroma as an Active Player in the Development of the Tumor Microenvironment.Cancer microenvironment : official journal of the International Cancer Microenvironment Society · 2015
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Revisiting the seed and soil in cancer metastasis.The international journal of biochemistry & cell biology · 2009
    Review
  9. Article
  10. Review
  11. Article
  12. HLA class I antigen processing machinery component expression and intratumoral T-Cell infiltrate as independent prognostic markers in ovarian carcinoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2008
    Article
  13. Examination of oral cancer biomarkers by tissue microarray analysis.Archives of otolaryngology--head & neck surgery · 2008
    Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Tumor escape mechanisms in prostate cancer.Cancer immunology, immunotherapy : CII · 2007
    Review
  19. Tumor stroma-associated antigens for anti-cancer immunotherapy.Cancer immunology, immunotherapy : CII · 2006
    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.

Graham PawelecCenter for Medical Research (ZMF), University of Tübingen, Waldhörnlestr. 22, 72072, Tübingen, Germany. graham.pawelec@uni-tuebingen.de
University of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although even "spontaneous" tumours are immunogenic and are commonly infiltrated by tumour antigen-specific T cells (at least in melanoma), most tumours are not completely rejected by the host, and cancer progresses. There is a growing realisation that many responses defined as antitumour effector mechanisms act as double-edged swords and under different conditions either become ineffective or even protumorigenic. Examples are interleukin 2 (also proapoptotic for activated T cells), interferon gamma (by induction of ligands for T and NK cell inhibitory receptors), angiogenesis inhibition (by hypoxia-mediated induction of growth factors promoting metastasis), and macrophage free radical-mediated cytotoxicity (by inhibiting T cells). Immune selection pressure itself, resulting in outgrowth of resistant tumour variants could also be viewed in this light. On the other hand, knowledge of the many tumour escape pathways offers the theoretical possibility of reconstituting antitumour immunity. Tumour escape from immunosurveillance represents the last series of hurdles to be overcome in formulating truly effective cancer immunotherapy, but given the immense plasticity of the tumour cell, and the complex balance between pro- and antitumour activity of the very same effector pathways, this remains a major challenge.

Indexed as

Antigens, NeoplasmHistocompatibility Antigens Class IHistocompatibility Antigens Class IIHumansInterleukin-10Interleukin-6Lymphocytes, Tumor-InfiltratingNeoplasmsSignal TransductionT-Lymphocytes, CytotoxicT-Lymphocytes, RegulatoryAntigens, NeoplasmHistocompatibility Antigens Class IHistocompatibility Antigens Class IIInterleukin-10Interleukin-6

Identifiers

PMID14685780
PMCPMC11032803
OpenAlexW2089045526

What OpenQuestion holds

Textmetadata
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.