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Record W2395533450 · doi:10.1158/1557-3125.advbc15-b45

Abstract B45: De novo generation of highly aggressive human breast tumors by rapid serial passaging of oncogene-transduced starting populations of purified normal cells

2016· article· en· W2395533450 on OpenAlexaff
Sylvain Lefort, Davide Pellacani, Long Nguyen, Connie J. Eaves

Bibliographic record

VenueMolecular Cancer Research · 2016
Typearticle
Languageen
FieldMedicine
TopicCancer Cells and Metastasis
Canadian institutionsTerry Fox Research Institute
Fundersnot available
KeywordsBiologyCancer researchMUC1MatrigelCarcinogenesisIn vivoProgenitor cellSyngenicXenotransplantationCD44Cell cultureCancerCellPathologyTransplantationImmunologyStem cellAngiogenesisAntigenCell biologyMedicineInternal medicine

Abstract

fetched live from OpenAlex

Abstract Human breast cancers are clonal outgrowths that have diversified genetically and biologically by the time they are clinically evident. However, early events that predicate malignant transformation of normal human mammary epithelial cells and the importance of the specific cell type to first be altered has remained elusive. We have developed an in vivo system that allows analysis of the initial steps of tumorigenesis from defined subsets of normal human mammary cells within 8 weeks using a single (KRASG12D) or multiple oncogenes. Using a protocol in which we first isolate biologically, transcriptionally and phenotypically different human mammary cell types by FACS using EpCAM and CD49f or CD10 as distinguishing markers, and then transduce the cells with lentiviral constructs, and immediately transplant them into highly immunodeficient NOD/RAG1-/-IL2rγ-/- (NRG) female mice, we have found that invasive ductal carcinomas expressing a variety of basal and luminal-associated markers (such as CK5, CK8/18, EGFR and MUC1) can be obtained at high frequency from purified starting populations of both basal cells and luminal progenitors within 8 weeks. Many tumours could be passaged both in vivo and under multiple conditions in vitro (on collagen, in suspension “mammopshere” culture or 3D matrigel cultures). After only 4passages in vivo, an aggressive tumor cell line that is tumorigenic within 6 weeks in vivo at unit efficiency has emerged. Intravenous injections shown that these cells can colonize multiple organs including the lung, kidney and spleen. Molecular characterization of these aggressive tumors has established that they are EpCAM+ and CD44+. Additional examples of de novo tumors able to be serially passaged are now being characterized. This new tumorigenesis model will allow us to compare the sequential changes that accompany and underlie the full process of malignant progression and should thus enable key molecular determinants that drive cancer initiation and progression to be identified. Citation Format: Sylvain Lefort, Davide Pellacani, Long Nguyen, Connie J. Eaves. De novo generation of highly aggressive human breast tumors by rapid serial passaging of oncogene-transduced starting populations of purified normal cells. [abstract]. In: Proceedings of the AACR Special Conference on Advances in Breast Cancer Research; Oct 17-20, 2015; Bellevue, WA. Philadelphia (PA): AACR; Mol Cancer Res 2016;14(2_Suppl):Abstract nr B45.

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 distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation 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 score0.016
Threshold uncertainty score0.557

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

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 head0.087
GPT teacher head0.384
Teacher spread0.297 · 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 teacher head, 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
Published2016
Admission routes1
Has abstractyes

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