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Record W2329053913 · doi:10.1158/1538-7445.am10-4551

Abstract 4551: 111In-NLS-Nimotuzumab: A potent auger electron-emitting radiotherapeutic agent for EGFR-overexpressing breast cancer

2010· article· en· W2329053913 on OpenAlexaffabout
R. M. REILLY, Ilia Tikhomirov

Bibliographic record

VenueCancer Research · 2010
Typearticle
Languageen
FieldMedicine
TopicRadiopharmaceutical Chemistry and Applications
Canadian institutionsAptose Biosciences (Canada)University of Toronto
Fundersnot available
KeywordsNLSChemistryNuclear localization sequenceInternalizationCytotoxicityCancer researchMolecular biologyClonogenic assayMonoclonal antibodyCellBiophysicsBiochemistryAntibodyBiologyIn vitroImmunologyCytoplasm

Abstract

fetched live from OpenAlex

Abstract Objective: To evaluate the cytotoxicity of nimotuzumab (Nmab), a monoclonal antibody specific for EGFR labeled with 111In and modified with nuclear localization sequence (NLS) peptides for importation into the nucleus of human breast cancer (BC) cells, where the emitted Auger electrons are most damaging to DNA and lethal. Methods: NMab was derivatized with sulfo-SMCC to introduce maleimide groups for reaction with NLS-peptides (CGYGPKKKRKVGG) and benzyl-DTPA (bn-DTPA) for complexing 111In. NLS substitution was quantified by a band shift on SDS-PAGE and bnDTPA substitution by an 111In-binding assay. The immunoreactivity (Kd) of NLS-Nmab was determined by the displacement of binding of 111In-Nmab to MDA-MB-468 BC cells (106 EGFR/cell). Internalization and nuclear importation were determined in MDA-MB-468 and MCF-7 (104 EGFR/cell) BC cells by subcellular fractionation at 37 oC and 4 oC up to 3 h. Clonogenic survival (CS) was measured in MDA-MB-468 and MCF-7 cells exposed to 2 to 40 nM (450-900 KBq/mL) of 111In-NLS-Nmab for 3 days. Results: Nmab was modified with 8.5±0.2 NLS and 2.1±2.1 bn-DTPA groups. The Kd for binding of 111In-NLS-Mab to MDA-MB-468 cells was 9.8±0.9 nM. NLS-Nmab was labeled with 111In to a radiochemical purity of 99.2±0.1% (specific activity 350±9 MBq/mg). The proportion of cell-bound 111In internalized into MDA-MB-468 cells at 3 h was 27.8±0.8% at 37 oC and 4.4±0.2 at 4 oC. Nuclear uptake was 31.2±2.6% for 111In-NLS-Nmab and 16.0±0.6% for 111In-Nmab (P<0.001). Binding and nuclear uptake were 20-fold and 6-fold lower, respectively for MCF-7 cells. The CS of MDA-MB-468 cells exposed to 111In-NLS-Nmab (20 nM) was 2.8±0.2% compared to 21.0±5.3% for 111In-Nmab (P=0.004) and 60.0±7.0% for Nmab (P=0.001). The CS of MCF-7 cells exposed to 111In-NLS-Nmab (40 nM) was 82.6±6.4% vs. 80.0±1.6% for 111In-Nmab (p>0.05) and 95±19.4% for Nmab (p>0.05). Conclusion: 111In-NLS-Nmab is a promising targeted radiotherapeutic agent for EGFR-overexpressing BC as evidenced by a 20-fold increased toxicity towards MDA-MB-468 cells compared to Nmab but lack of toxicity towards MCF-7 cells with 10-fold lower EGFR expression similar to that on most normal epithelial cells. Supported by the Canadian Breast Cancer Research Alliance (Grant 019513). Citation Format: {Authors}. {Abstract title} [abstract]. In: Proceedings of the 101st Annual Meeting of the American Association for Cancer Research; 2010 Apr 17-21; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2010;70(8 Suppl):Abstract nr 4551.

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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 score0.004

Distilled classifier scores by category (both heads)

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

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 head0.098
GPT teacher head0.483
Teacher spread0.385 · 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".

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Citations0
Published2010
Admission routes2
Has abstractyes

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