Evidence map›Paper›PMID 19935793›Full record

ArticleBritish journal of cancer2010

Immunophenotype and molecular characterisation of adenocarcinoma of the small intestine.

M J Overman, J Pozadzides, S Kopetz, S Wen, J L Abbruzzese, R A Wolff, H Wang

Abstract read
In one paragraph

Article in British journal of cancer, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

61 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  18. Small bowel adenocarcinoma: An overview.World journal of gastrointestinal oncology · 2022
    Review
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1 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

M J OvermanDepartment of Gastrointestinal Medical Oncology, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030, USA. moverman@mdanderson.org
J Pozadzides
S Kopetz
S Wen
J L Abbruzzese
R A Wolff
H Wang

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite having a dramatically larger surface area than the large intestine, the small intestine is an infrequent site for the development of adenocarcinoma. To better understand the molecular abnormalities in small bowel adenocarcinoma (SBA), we characterised a number of candidate oncogenic pathways and the immunophenotype of this rare cancer.

methodsTissue microarrays were constructed from tumour samples from 54 patients with all stages of the disease. Immunohistochemistry and microsatellite instability (MSI) testing were conducted.

resultsThe profile of cytokeratin 20 and 7 coexpression was variable, but expression of caudal type homeobox transcription factor 2 (CDX2) was present in 70% of cases. In this young population (median age 54 years), loss of mismatch repair (MMR) proteins occurred in 35% of patients, with confirmed MSI in 100% of tested cases. Expression of vascular endothelial growth factor-A (VEGF-A) and epidermal growth factor receptor (EGFR) was common, occurring in 96 and 71% of patients, respectively. Only one case showed HER2 expression and none showed loss of phosphatase and tensin homologue mutated on chromosome 10 (PTEN).

conclusionsThese results suggest that alterations in DNA MMR pathways are common in SBAs, similar to what is observed in large bowel adenocarcinomas. Furthermore, the high percentage of tumours expressing both EGFR and VEGF suggests that patients with this rare cancer may benefit from therapeutic strategies targeting EGFR and VEGF receptor (VEGFR).

Indexed as

Gene Expression ProfilingImmunophenotypingOncogenesAdenocarcinomaAdultAgedCDX2 Transcription FactorDNA Mismatch RepairDuodenal NeoplasmsErb-b2 Receptor Tyrosine KinasesErbB ReceptorsFemaleGenes, erbB-1Genes, erbB-2Homeodomain ProteinsHumansCDX2 protein, humanCDX2 Transcription FactorEGFR protein, humanERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesErbB ReceptorsHomeodomain ProteinsKeratinsNeoplasm ProteinsPTEN PhosphohydrolasePTEN protein, humanReceptors, Vascular Endothelial Growth Factor

Identifiers

PMID19935793
PMCPMC2813754

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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.