Inhibition of CBP/p300 bromodomain activity increases chemosensitivity of p53 mutant colorectal cancers through inhibiting p53 aggregation
抑制 CBP/p300 溴结构域活性通过抑制 p53 聚集增加 p53 突变结直肠癌的化疗敏感性
基本信息
- 批准号:472399
- 负责人:
- 金额:$ 7.29万
- 依托单位:
- 依托单位国家:加拿大
- 项目类别:Operating Grants
- 财政年份:2022
- 资助国家:加拿大
- 起止时间:2022-09-01 至 2023-09-01
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
p53 mutations are found in over 50% of cancers and are often associated with a worse outcome for patients. It is well established that chemotherapy can cause mutant p53 to form aggregates, hereafter refered to as protein "clumps". We uncovered a previousl
p53突变在超过50%的癌症中发现,并且通常与患者的更差结果相关。众所周知,化疗可导致突变型p53形成聚集体,下文称为蛋白质“团块”。我们发现了一个
项目成果
期刊论文数量(0)
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O'Brien Catherine A其他文献
O'Brien Catherine A的其他文献
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{{ truncateString('O'Brien Catherine A', 18)}}的其他基金
Molecular drivers of the drug tolerant persister state in patient-derived colorectal cancer models
患者来源的结直肠癌模型中耐药持续状态的分子驱动因素
- 批准号:
434963 - 财政年份:2020
- 资助金额:
$ 7.29万 - 项目类别:
Operating Grants
Colorectal cancer stem cell plasticity: A novel therapeutic target
结直肠癌干细胞可塑性:一个新的治疗靶点
- 批准号:
334266 - 财政年份:2015
- 资助金额:
$ 7.29万 - 项目类别:
Operating Grants
Targeting colorectal cancer-initiating cells and anti-EGFR therapeutic resistance by manipulating levels of the reactive aldehyde, 4-hydroxynonenal.
通过控制活性醛 4-羟基壬烯醛的水平,靶向结直肠癌起始细胞和抗 EGFR 治疗耐药性。
- 批准号:
302201 - 财政年份:2013
- 资助金额:
$ 7.29万 - 项目类别:
Salary Programs
Targeting colorectal cancer-initiating cells and anti-EGFR therapeutic resistance by manipulating levels of the reactive aldehyde, 4-hydroxynonenal
通过控制活性醛 4-羟基壬烯醛的水平,靶向结直肠癌起始细胞和抗 EGFR 治疗耐药性
- 批准号:
281581 - 财政年份:2013
- 资助金额:
$ 7.29万 - 项目类别:
Operating Grants
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