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Record W2332184346 · doi:10.1158/1538-7445.am2011-5105

Abstract 5105: Towards a multiparametric biomarker panel for pancreatic cancer detection

2011· article· en· W2332184346 on OpenAlexaff
Shalini Makawita, Christopher R. Smith, Ihor Batruch, Felix Rueckert, Eleftherios P. Diamandis

Bibliographic record

VenueCancer Research · 2011
Typearticle
Languageen
FieldMedicine
TopicPancreatic and Hepatic Oncology Research
Canadian institutionsMount Sinai HospitalUniversity Health NetworkUniversity of Toronto
Fundersnot available
KeywordsPancreatic cancerCancerBiomarkerProteomeProteomicsBiomarker discoveryCancer researchMedicineBiologyComputational biologyPathologyOncologyInternal medicineBioinformaticsBiochemistry

Abstract

fetched live from OpenAlex

Abstract Pancreatic cancer is one of the most highly lethal of all solid malignancies for which serological biomarkers to aid in the detection and clinical management of patients are urgently needed. To date, the lack of a single highly specific and sensitive marker for pancreatic cancer detection has led to a growing consensus in the field towards the development of panels of biomarkers, where-by the combinatorial assessment of multiple biomarkers will likely result in increased sensitivity and specificity. In this respect, we previously characterized the conditioned media of six pancreatic cancer cell lines (MIA-PaCa2, BxPc3, PANC1, Su.86.86, CAPAN1, CFPAC1) and the normal human pancreatic ductal epithelial cell line HPDE, as well as six pancreatic juice samples from pancreatic ductal adenocarcinoma patients using strong cation exchange followed by reverse-phase coupled online to an LTQ-Orbitrap mass spectrometer. This resulted in the identification of 3810 non-redundant proteins in the cell lines and 648 proteins in the pancreatic juice. All proteins were identified with 2 or more peptides. Through subsequent bioinformatic analyses which included hierarchical clustering, label-free protein quantification between the cancer and normal cell lines, cellular localization, tissue specificity and integration of the proteomes from the multiple biological fluids, a list of candidate pancreatic cancer biomarkers was generated. Preliminary verification of selected candidates using enzyme-linked immunosorbent assays (ELISAs) in a screening set of plasma samples from pancreatic cancer patients and healthy age-sex matched controls (n=40) show five proteins (designated PANC1, PANC2, PANC3, PANC4 and PANC5) to be significantly increased in pancreatic cancer plasma (p=0.0011, p<0.0001, p<0.0001, p<0.0001 and p=0.0098, respectively). Individually, these proteins did not exhibit improved area under the curve (AUC) in comparison to CA19.9 levels measured in the same samples; however the combination of the five proteins with CA19.9 showed improved AUC to CA19.9 alone (CA19.9 alone AUC = 0.97; all proteins with CA19.9 AUC = 1.0). These data suggest that this novel panel warrants further evaluation as a pancreatic cancer diagnostic tool. 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 5105. doi:10.1158/1538-7445.AM2011-5105

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)0.002
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.002
Threshold uncertainty score0.008

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0020.001
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0020.001
Science and technology studies0.0000.000
Scholarly communication0.0010.001
Open science0.0010.001
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0020.002

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 head0.404
GPT teacher head0.492
Teacher spread0.088 · 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 designObservational
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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