Evidence map›Paper›PMID 18581998›Full record

ArticleCancer immunity2008

Identification of tumor-associated antigens by large-scale analysis of genes expressed in human colorectal cancer.

Pedro M S Alves, Nicole Lévy, Brian J Stevenson, Hanifa Bouzourene, Grégory Theiler, Gabriel Bricard, Sebastien Viatte, Maha Ayyoub, Henri Vuilleumier, Jean-Claude R Givel and 5 more

Open access · greenAbstract read
In one paragraph

Article in Cancer immunity, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 14% 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, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Microorganisms · 2024
    Review
  5. Article
  6. Review
  7. Human Endogenous Retroviruses in Diseases.Sub-cellular biochemistry · 2023
    Article
  8. Article
  9. Up-regulation of MARVEL domain-containing protein 1 (MARVELD1) accelerated the malignant phenotype of glioma cancer cells via mediating JAK/STAT signaling pathway.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2021
    Article
  10. Review
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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

15 authors at 1 institution in 1 country.

Pedro M S AlvesNational Center of Competence in Research, Molecular Oncology, ISREC, Ch. des Boveresses 155, 1066 Epalinges, Switzerland.
Nicole Lévy
Brian J Stevenson
Hanifa Bouzourene
Grégory Theiler
Gabriel Bricard
Sebastien Viatte
Maha Ayyoub
Henri Vuilleumier
Jean-Claude R Givel
Donata Rimoldi
Daniel E Speiser
C Victor Jongeneel
Pedro J Romero
Frédéric Lévy
Swiss Institute of Comparative Law · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the high prevalence of colon cancer in the world and the great interest in targeted anti-cancer therapy, only few tumor-specific gene products have been identified that could serve as targets for the immunological treatment of colorectal cancers. The aim of our study was therefore to identify frequently expressed colon cancer-specific antigens. We performed a large-scale analysis of genes expressed in normal colon and colon cancer tissues isolated from colorectal cancer patients using massively parallel signal sequencing (MPSS). Candidates were additionally subjected to experimental evaluation by semi-quantitative RT-PCR on a cohort of colorectal cancer patients. From a pool of more than 6000 genes identified unambiguously in the analysis, we found 2124 genes that were selectively expressed in colon cancer tissue and 147 genes that were differentially expressed to a significant degree between normal and cancer cells. Differential expression of many genes was confirmed by RT-PCR on a cohort of patients. Despite the fact that deregulated genes were involved in many different cellular pathways, we found that genes expressed in the extracellular space were significantly over-represented in colorectal cancer. Strikingly, we identified a transcript from a chromosome X-linked member of the human endogenous retrovirus (HERV) H family that was frequently and selectively expressed in colon cancer but not in normal tissues. Our data suggest that this sequence should be considered as a target of immunological interventions against colorectal cancer.

Indexed as

Gene Expression ProfilingGene Expression Regulation, NeoplasticAntigens, NeoplasmBiomarkers, TumorColorectal NeoplasmsDown-RegulationEndogenous RetrovirusesHumansAntigens, NeoplasmBiomarkers, Tumorcolon-specific antigen

Identifiers

PMID18581998
PMCPMC2935784
OpenAlexW2118541620

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.