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Record W2086609246 · doi:10.1158/1538-7445.am2011-3906

Abstract 3906: Gene expression profiling of ductal carcinoma in situ reveals novel alterations in the tumor and stromal compartments related to progession and outcome of invasive breast cancer

2011· article· en· W2086609246 on OpenAlexaff
Agnieszka K. Witkiewicz, Adam Ertel, Jessica Kline, Elai Davicioni, Erik S. Knudsen

Bibliographic record

VenueCancer Research · 2011
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicCancer-related molecular mechanisms research
Canadian institutionsGenome British Columbia
Fundersnot available
KeywordsMyoepithelial cellBiologyDuctal carcinomaStromal cellBreast cancerMetastasisGene expression profilingCancer researchPathologyGene expressionGene signatureCancerEstrogen receptorGeneMedicineImmunohistochemistryImmunologyGenetics

Abstract

fetched live from OpenAlex

Abstract An increasing number of women are diagnosed with ductal carcinoma in situ (DCIS). DCIS is non-obligate precursor to invasive breast cancer. Mechanisms leading to development and progression of DCIS to invasive breast cancer (IBC) are still largely unknown. When DCIS and IBC coexist in the same lesion, their transcriptional profiles are nearly identical; however, there are very few studies investigating gene expression in pure DCIS. The goal of this study was to compare gene expression profiles of microdissected epithelial and stromal components of pure DCIS and IBC. Epithelium and stroma were laser microdissected from 10 cases of pure DCIS and 10 invasive breast carcinomas. DCIS and IBC were matched with regard to estrogen, progesterone receptor and HER2 expression. Gene expression was analyzed using Affymetrix Human Exon 1.0 ST microarrays. Analyses of gene expression in IBC and DCIS revealed a number of differentially expressed genes in the epithelial (n=211) and stromal (n=143) LCM obtained cells. In the epithelial compartment many of the genes specifically associated with IBC are part of previously described epithelial to mesenchymal transition, metastasis and myoepithelial cell gene expression signatures. Consistent with these findings, gene ontology analyses found overrepresentation of GO Biological Process terms such as ‘cell adhesion’ (44 genes, p = 1.47E-14), ‘extracellular matrix organization’ (16 genes, p = 3.46E-09), ‘skeletal system development’ (22 genes, p = 5.87E-07) and ‘vasculature development’ (14 genes, P = 4.56E-03). Applying differentially expressed epithelial genes to a larger invasive breast cancer dataset showed association with decreased metastasis free and progression free survival. Our study reveals that pure dcis and invasive breast cancer are distinct at the transcriptome level. Future work will show if genes differentially expressed between IBC and pure DCIS may be useful for identifying at the time of diagnosis DCIS patients likely to progress to IBC. Citation Format: {Authors}. {Abstract title} [abstract]. In: Proceedings of the 102nd Annual Meeting of the American Association for Cancer Research; 2011 Apr 2-6; Orlando, FL. Philadelphia (PA): AACR; Cancer Res 2011;71(8 Suppl):Abstract nr 3906. doi:10.1158/1538-7445.AM2011-3906

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.001
Threshold uncertainty score0.005

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.001
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.079
GPT teacher head0.382
Teacher spread0.303 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2011
Admission routes1
Has abstractyes

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