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Abstract B44: Probing the effects of linker flexibility in second mitochondria-derived activator of caspases mimetic dimers and assessing their ability to induce apoptosis in a MDA-MB-231 cell line

2010· article· en· W1986849223 on OpenAlexaff
Taz Cheema, Robert N. Ben, Herman Cheung, Eric C. LaCasse

Bibliographic record

VenueClinical Cancer Research · 2010
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicMitochondrial Function and Pathology
Canadian institutionsChildren's Hospital of Eastern OntarioUniversity of Ottawa
Fundersnot available
KeywordsXIAPCaspaseApoptosisInhibitor of apoptosisProgrammed cell deathActivator (genetics)ProteasesIntrinsic apoptosisAmino acidCancer cellCell biologyChemistryBiochemistryBiologyMolecular biologyEnzymeReceptorCancerGenetics

Abstract

fetched live from OpenAlex

Abstract Programmed cell death (apoptosis) is the most common mechanism of cell death in eukaryotes. The ability of cancer cells to evade and inhibit apoptosis has become a hallmark feature of cancer. This is accomplished through a family of proteins known as the inhibitor of apoptosis proteins (lAPs). X-linked inhibitor of apoptosis protein (XIAP) is one of the best characterized lAPs. XIAP suppresses apoptosis by forming complexes with cysteine-aspartic proteases (caspase), in particular caspase −3, −7, and −9 through one of its baculovirus IAP repeat (BIR) domains. Second mitochondria-derived activator of caspases (SMAC) is an antagonist protein released from the mitochondria and into the cytosol, to disrupt the complexes produced between XIAP and caspase. SMAC binds to the BIR domains in XIAP through its tetra-peptide motif, AVPI. Studies have demonstrated that the first and third amino acid positions of this tetra-peptide motif are important for binding, while positions two and four can be modified to increase binding affinity (AXPX). It has also been shown that dimers of SMAC mimetics show greater potency than their monomer counter parts. Previously, our laboratory has synthesized and tested SMAC dimers using three glycine amino acids to link AXPX sequences. These compounds showed very little activity. We also synthesized and tested SMAC dimers comprised of a lysine amino acid, linking two AXPX sequences; these mimetics did display significant activity. In particular an (AKPF)2K sequence showed 50% cell death at 10 uM when combined with death ligand TRAIL. Synthesis of these compounds was conducted using solid phase peptide synthesis (SPPS) on a polystyrene resin. We hypothesized that flexibility in the linker joining the two AXPX sequences was necessary to increase binding affinity. Consequently several SMAC mimetic dimers built on two different linkers (gamma-amino butyric acid and ornithine), both of which have a four carbon spacer between each terminus, have been prepared and evaluated for activity using a MDA-MB-231 breast cancer cell line. The first series of SMAC mimetic compounds consists of MeAXPX-GABA-MeAXPX amino acid sequence while the second series of SMAC mimetics are comprised of a MeAXPX-Ornithine-XPXMeA amino acid sequence. All data and results, including synthesis, biological assays, and the testing of these compounds will be the major focus of this presentation. Citation Information: Clin Cancer Res 2010;16(14 Suppl):B44.

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 score0.004

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 integrity0.0000.001
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 head0.088
GPT teacher head0.432
Teacher spread0.345 · 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
Published2010
Admission routes1
Has abstractyes

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