Evidence map›Paper›PMID 21990607›Full record

ArticleJournal of dental research2012

Unique FISH patterns associated with cancer progression of oral dysplasia.

C F Poh, Y Zhu, E Chen, K W Berean, L Wu, L Zhang, M P Rosin

Abstract read
In one paragraph

Article in Journal of dental research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

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

  1. Pooled it
  2. Recurrent copy number alterations involving EGFR, CDKN2A, and CCND1 in oral premalignant lesions.Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology · 2022
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  3. 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

7 authors.

C F PohDepartment of Oral Biological and Medical Science, the University of British Columbia, 2199 Wesbrook Mall, Vancouver, BC, Canada. cpoh@interchange.ubc.ca
Y Zhu
E Chen
K W Berean
L Wu
L Zhang
M P Rosin

Funding

Optical Techniques and Oral Precancer ManagementR01DE017013 · NIDCR · BRITISH COLUMBIA CANCER AGENCY · PI ROSIN, MIRIAM P. · 2005 to 2009
$1.9M
CIHR MOP-77663NIDCR NIH HHS R01 DE017013NIDCR NIH HHS R01DE17013
6 · The paper itself

Abstract

Subgroups of patients with oral pre-malignant lesions (OPLs) are at extremely high risk for developing invasive cancer in spite of surgical excision. The objective of this study was to evaluate the utility of specific genes and their associated centromeres as markers to stratify OPLs for their cancer risk. Samples used in this study included 35 oral dysplasia with known outcome and 20 normal oral mucosa. Of the dysplasias, 20 were from an ongoing longitudinal study showing progression. The remaining 15 cases (2 of which progressed) were chosen from the population-based, provincial BC Oral Biopsy Service (OBS). Copy number alterations at EGFR, CEP7, CCND1, and CEP11 were evaluated by fluorescent in situ hybridization (FISH). There was no significant difference in demographics between progressors and non-progressors. Specific FISH profiles at these genes and their corresponding centromeres were associated with progression. High gene gain of CCND1 was associated with an 8-fold elevated risk of progression compared with those with no gain in time-to-progression analysis. Numerical alterations of EGFR and CCND1 and their centromeres might be an effective means for identifying OPLs at risk. Future studies will expand on this analysis and set the stage for application of this approach in routine clinical practice.

Indexed as

Biomarkers, TumorCarcinoma, Squamous CellCase-Control StudiesCell Transformation, NeoplasticCentromereChromosomal InstabilityCyclin D1Disease ProgressionErbB ReceptorsFemaleGene DosageHumansIn Situ Hybridization, FluorescenceKaplan-Meier EstimateMaleMiddle AgedBiomarkers, TumorCCND1 protein, humanCyclin D1EGFR protein, humanErbB Receptors

Identifiers

PMID21990607
PMCPMC3232118

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.