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Record W2313634730 · doi:10.1158/1538-7445.am2011-4870

Abstract 4870: High-throughput proteomics using stable isotope labelling with amino acids in cell culture (SILAC) reveals potential modulators of androgen-independent prostate cancers

2011· article· en· W2313634730 on OpenAlexaff
Punit Saraon, Ihor Batruch, Christopher R. Smith, Atsushi Mizokami, Keith Jarvi, Eleftherios P. Diamandis

Bibliographic record

VenueCancer Research · 2011
Typearticle
Languageen
FieldChemistry
TopicAdvanced Proteomics Techniques and Applications
Canadian institutionsUniversity Health NetworkUniversity of TorontoMount Sinai Hospital
Fundersnot available
KeywordsLNCaPStable isotope labeling by amino acids in cell cultureProstate cancerAndrogenAndrogen receptorCancer researchBiologyAndrogen deprivation therapyInternal medicineProteomicsEndocrinologyChemistryCancerBiochemistryMedicineHormoneGenetics

Abstract

fetched live from OpenAlex

Abstract Prostate cancer is the most common malignancy and the second leading cause of cancer related deaths in men. One common treatment is androgen-deprivation therapy, which reduces symptoms in most patients. However, over time patients develop tumours that are androgen-independent and ultimately fatal. The mechanisms that cause this transition remain largely unknown, and as a result, there are no effective treatments against androgen-independent prostate cancer. As a model for androgen-independence, we used the LNCaP cell line which is naturally androgen-dependent grown in androgen depleted conditions for a 6 month period to generate the androgen-independent cell line LNCaP-SF. Preliminary experiments showed that the LNCaP-SF cell line had higher proliferation/viability rates in androgen-depleted conditions, and had increased expression of the androgen receptor protein, a key modulator in prostate cancer progression. Our next goal was to assess to differential global protein expression as well as differential expression of secreted proteins from each of the two cell lines. To identify differentially expressed proteins, we utilized Stable Isotope Labelling with Amino Acids in Cell Culture (SILAC) coupled to mass spectrometry. LNCaP cells were labelled in growth media containing light-Arg/Lys whereas LNCaP-SF was labelled in heavy Arg-Lys media. After proteomic analysis, we were able to quantify 3355 proteins with at least one peptide hit. From these proteins, using stringent criteria, 99 and 82 proteins were found to be up-regulated and down-regulated respectively, in LNCaP-SF cells compared to LNCaP cells. Using various bioinformatics tool, we found that genes involved in fatty acid degradation and ketogenesis as important pathways that with over-expressed in LNCaP-SF cells. We performed qPCR validation of genes involved in each of these pathways and found that LNCaP-SF cells generally had an increase in the expression of many these genes, compared to LNCaP cells. These preliminary results show that genes involved in fatty acid degradation and ketogenesis pathways could serve as potential biomarkers for androgen-independent prostate cancer. 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 4870. doi:10.1158/1538-7445.AM2011-4870

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 score0.002
Threshold uncertainty score0.007

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0020.001

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 head0.051
GPT teacher head0.336
Teacher spread0.285 · 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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