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Record W2530387696

Identification Of Novel Monocytoid Cell Activators To Reduce Brain Tumour Initiating Cell Growth

2013· article· en· W2530387696 on OpenAlexaffvenue
Yibo Li

Bibliographic record

VenueJournal of undergraduate research in Alberta · 2013
Typearticle
Languageen
FieldMedicine
TopicGlioma Diagnosis and Treatment
Canadian institutionsUniversity of Calgary
Fundersnot available
KeywordsMicrogliaNeurosphereGliomaCancer cellCell typeCancer researchCell cultureImmune systemBiologyStem cellCellImmunologyMedicineCancerPathologyCellular differentiationCell biologyInternal medicineInflammationBiochemistryAdult stem cell
DOInot available

Abstract

fetched live from OpenAlex

INTRODUCTION Malignant gliomas are the most common and deadly type of adult brain tumours. Brain tumour initiating cells (BTICs), a type of cancer stem cell, have been identified to contribute to the tumourigenesis and recurrence of gliomas. Surrounding BTICs in situ are monocytoid cells, which are innate immune cells of the central nerve system (CNS) (microglia) or cells which have infiltrated into the CNS (macrophages). Though thought to be initially recruited to eradicate the tumours, these cells are ultimately exploited by the tumour cells to promote their own growth. Thus, activating or reprogramming monocytoid cells may represent an approach to curb BTIC growth. Previously, a drug screen of 1040 compounds for their capacity to further activate lipopolysaccharide (LPS)-stimulated human microglia identified niacin, orlistat, bumetanide and meclocycline as hits [1]; demeclocycline was subsequently added to the list. METHODS Human adult and fetal microglia and human blood monocytes were plated at 50,000 cells/well/100μL and 100,000 cells/well/100μL, respectively, in 96-well plates, and transferred to BTIC medium an hour prior to treatment. Treatment involved administering each drug (10 μM) with and without LPS (100 ng/mL). Media were collected 48 hrs after treatment and termed microglia/monocyte conditioned medium (MCM/Mono CM). BTIC cells derived from glioma patients were exposed at 10,000 cells/well/100μL with either MCM or Mono CM in 96-well plates for 72 hrs. The number of neurospheres above 60 microns was counted with the assistance of a light microscope (n = 4 per well) for neurosphere assay analysis. RESULTS Microglia-conditioned media (MCM) generated in the presence of LPS and each drug attenuated growth of patient-derived BTICs in vitro when compared to LPS-MCM alone. Notably, these drugs also promoted BTIC differentiation into cells which exhibited reduced stemness.  A similar effect was observed with monocyte-conditioned media (Mono CM) with all four drugs in the presence of LPS (Figure 1). Interestingly, a combination of demeclocycline and niacin also reduced BTIC growth without the need for LPS. DISCUSSION AND CONCLUSIONS This study has verified a number of promising candidates for harnessing innate immune cells in the glioma micro-environment to curb BTIC growth, paving the way for future approaches to clinically targeting BTIC growth. Future directions could test combinations of drugs with alternatives to LPS, such as amphotericin B, a recently observed activator of monocytoid cells, and compounds observed endogenously, such as interleukin-1β and interferon gamma, which could lead to identifying more clinically-viable options. REFERENCES Samanani S, et al. CNS Neurol Disord Drug Targets. 12 :741-9, 2013. Zhai H, et al. Glia . 59 :472-85, 2011.

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 score0.003
Threshold uncertainty score0.009

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)0.0030.001

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 head0.066
GPT teacher head0.367
Teacher spread0.301 · 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
Published2013
Admission routes2
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