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Record W7005958473

Role of histone methylation in the regulation of tumour suppressor networks

2016· dissertation· en· W7005958473 on OpenAlexfundno aff

Bibliographic record

VenueeScholarship@McGill (McGill) · 2016
Typedissertation
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicLepidoptera: Biology and Taxonomy
Canadian institutionsnot available
FundersNational Cancer InstituteCanadian Institutes of Health ResearchTerry Fox Foundation
KeywordsHistoneSuppressorDNA methylationEpigeneticsMethylationHistone H2A
DOInot available

Abstract

fetched live from OpenAlex

Cellular senescence is a tumour suppressor mechanism which prevents the proliferation of malignant cells.In normal cells, oncogenic stimuli induce a senescence response and growth arrest coordinated by tumour suppressor genes, but the loss of expression of these genes impairs the establishment of senescence in cancer cells.We studied the role of histone methylation and oncogenic histone modifiers to assess their responsibility throughout the bypass of tumour suppressor pathways.We first used a PRMT6 knock-out mouse model to recognize the potential effect of PRMT6mediated histone arginine methylation in cancer.Herein, we report that PRMT6 catalyzes the asymmetric di-methylation of histone H3 at arginine R2 (H3R2me2a) inside the promoter region of the Trp53 gene, resulting in the transcriptional repression of p53.In mice, functional inactivation of p53 is sufficient to bypass oncogene-induced senescence (OIS).We demonstrated that the overexpression of PRMT6 cooperates with oncogenic Ras in the bypass of OIS, suggesting an important role for histone arginine methylation mediated by PRMT6 in promoting tumourigenesis.In the second part of my thesis, I describe miR-137 as an inhibitor of KDM4A expression.KDM4A is a histone lysine demethylase participating in gene repression and the bypass of OIS to promote tumourigenesis in vivo.Specifically, KDM4A targets CHD5, a tumour suppressor and positive regulator p53 expression.We observed that miR-137 expression is lost in Ras-dependent pancreatic cancer.Moreover, restoration of its expression led to cellular growth arrest and senescence in pancreatic cancer cells.We used short hairpin inhibitors of p53 and p16 INK4A to dissect the senescence pathways controlled by miR-137 and noticed that both ARF/p53 and p16 INK4A /pRb tumour suppressor pathways were independently induced by miR-137.Importantly, expression of miR-137 is enhanced upon Ras activation, and the inhibition of miR-137 activity led to the bypass of OIS.These results suggest that miR-137 targets KDM4A to mediate senescence in response to oncogenic Ras, and that silencing of miR-137 could promote the Ras-driven transformation of pancreatic cancer cells.The work presented in this thesis emphasizes on the importance of the senescence response in tumour suppression.Our results provide a connection between deregulated histone methylation and defective OIS signaling in cancer.I propose that modulating the enzymes responsible for the repression of tumour suppressor genes could be a promising avenue in the prevention or treatment of cancer.

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: Not applicable · Consensus signal: none
GenreCandidate signal: Other · Consensus signal: none
Teacher disagreement score0.003
Threshold uncertainty score0.000

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 communication0.0010.000
Open science0.0000.000
Research integrity0.0000.000
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 head0.010
GPT teacher head0.248
Teacher spread0.238 · 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 designNot applicable
Domainnot available
GenreOther

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
Published2016
Admission routes1
Has abstractyes

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