Evidence map›Paper›PMID 20002690›Full record

ArticleColorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland2011

The role of cell proliferation and crypt fission in adenoma aggressiveness: a comparison of ileoanal pouch and rectal adenomas in familial adenomatous polyposis.

O C C Will, M Deheragoda, R K S Phillips, S K Clark, I P M Tomlinson

Abstract readComparative Study
In one paragraph

Article in Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact, top 92% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

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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

5 authors at 4 institutions in 1 country.

O C C Will *The Polyposis Registry, St Mark's Hospital, Harrow, UK.
M Deheragoda *London Research Institute, Cancer Research UK, London, UK.
R K S PhillipsThe Polyposis Registry, St Mark's Hospital, Harrow, UK.
S K ClarkThe Polyposis Registry, St Mark's Hospital, Harrow, UK.
I P M TomlinsonWellcome Trust Institute for Human Genetics, Oxford, UK.
St Mark's Hospital · GBCancer Research UK · GBCentre for Human Genetics · GBUniversity College Hospital · GB

Funding

Cancer Research UKWellcome Trust 084818Wellcome Trust 090532
6 · The paper itself

Abstract

aimIn patients with familial adenomatous polyposis (FAP), ileoanal pouch cancer is rare whereas rectal cancer is common, despite polyp initiation at the two sites being similar at the molecular level. This study investigated whether the disparity in adenoma aggressiveness reflects underlying differences in histogenesis.

methodNormal mucosal biopsies and 2-3 mm adenomas from patients with FAP were dissected into individual crypts. Crypt area, morphology, fission and mitoses were analysed for crypts from pouch, rectum and supra-anastomotic ileum. Immunohistochemistry of similar archival samples was performed for lysozyme, β-catenin and TP53 expression.

resultsThe morphology of normal crypts was similar at each site, although crypt area differed. The area of normal pouch crypts was intermediate between rectum and ileum. The area of adenomatous crypts of rectum and pouch was similar, but the latter had increased asymmetrical fission. Crypt mitoses were proportional to area in all tissues, but crypt fission was reduced in adenomatous crypts from the rectum compared with the pouch. Pouch adenomas retained lysozyme expression as seen in normal ileum. Nuclear β-catenin accumulation was similar, but TP53 expression was increased in rectal adenomas.

conclusionDiminutive polyps from rectum and pouch differ in morphology and proliferation. Aggressiveness in rectal polyps is not conferred by increased crypt proliferation, fission, or activation of the Wnt signalling pathway. Increased TP53 expression suggests other molecular mechanisms may be responsible. While crypt mitoses are proportional to crypt area, the threshold for fission may be site specific, indicating that tissue origin may influence histogenesis and thus malignant potential.

Indexed as

Cell ProliferationAdenomaAdenomatous Polyposis ColiAdenomatous Polypsbeta CateninBiopsyColonic PouchesDisease ProgressionHumansIntestinal MucosaIntestinal PolypsRectal NeoplasmsTumor Suppressor Protein p53beta CateninCTNNB1 protein, humanTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID20002690
PMCPMC4610058
OpenAlexW1940008050

What OpenQuestion holds

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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.