Evidence map›Paper›PMID 10193318›Full record

ArticleJournal of clinical pathology1998

De novo expression of CD44 in prostate carcinoma is correlated with systemic dissemination of prostate cancer.

V Paradis, P Eschwège, S Loric, F Dumas, N Ba, G Benoît, A Jardin, P Bedossa

Open access · bronzeAbstract read
In one paragraph

Article in Journal of clinical pathology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

11 citing papers in PubMed, 35 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

8 authors at 3 institutions in 1 country.

V ParadisService d'Anatomie Pathologique, Hôpital de Bicêtre, Paris, France. vparadis@teaser.fr
P Eschwège
S Loric
F Dumas
N Ba
G Benoît
A Jardin
P Bedossa
Sorbonne Université · FRBicêtre Hospital · FRHôpital Tenon · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsTo evaluate the role of CD44 in early steps in the development of prostate cancer, and to assess the biological significance of preneoplastic lesions in prostate cancer.

methods38 patients with clinically localised prostate cancer were studied. The standard form of CD44 (CD44H) and v6 isoform expressions were semiquantitatively evaluated on paraffin embedded tumour tissue by immunohistochemistry. Disseminated prostatic cells were detected by prostate specific membrane antigen reverse transcriptase polymerase chain reaction in the blood of each patient before radical prostatectomy.

resultsIn normal or benign prostate glands, only basal cells showed CD44H and v6 labelling. Fourteen of the 38 prostate cancers (37%) had CD44H membranous staining of prostatic tumour cells. In 18 patients (47%), circulating prostatic cells were detected in blood before surgery. Although no correlation between the expression of CD44 and the Gleason score or staging was observed, a significant correlation was found between the expression of CD44H by tumour cells and prostatic cell blood dissemination (p = 0.04). In 28 cases, foci of prostatic intraepithelial neoplasia were observed, and nine had CD44H immunostaining.

conclusionsDe novo expression of CD44 by prostatic tumour cells is associated with systemic dissemination of prostate cells independently of pathological criteria.

Indexed as

AdultAgedAntigens, NeoplasmBiomarkers, TumorCarcinoma, Acinar CellDisease ProgressionFollow-Up StudiesHumansHyaluronan ReceptorsImmunoenzyme TechniquesMaleMiddle AgedNeoplastic Cells, CirculatingProstatic Intraepithelial NeoplasiaProstatic NeoplasmsReverse Transcriptase Polymerase Chain ReactionAntigens, NeoplasmBiomarkers, TumorHyaluronan Receptors

Identifiers

PMID10193318
PMCPMC500969
OpenAlexW2148644797

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.