Investigating The Importance Of Mutations In The Estrogen Receptor-a Gene In Breast Cancer
Investigating The Importance Of Mutations In The Estrogen Receptor-a Gene In Breast Cancer
批准号:
2022896
负责人:
金额:
$0.0万
依托单位:
依托单位国家:
英国
项目类别:
Studentship
财政年份:
2017
资助国家:
英国
项目状态:
已结题
起止时间:
2017 至 --
中文摘要
乳腺癌是全世界女性中最常见的癌症,每年确诊病例超过150万例。每年有50万妇女死于这种疾病。乳腺癌的一个关键驱动因素是雌激素,它通过激活雌激素受体蛋白(ERa)起作用。我们已经使用CRISPR-Cas9基因组编辑系统在研究充分且广泛使用的雌激素应答型MCF7乳腺癌细胞系中制作基因敲入蛋白,以模拟最近在治疗耐药,转移性乳腺癌(endo - mbc)中发现的主要ERa突变。这些工程细胞系是一种独特而复杂的细胞资源,其目的是研究这些突变如何起作用,评估它们在转移中的作用,更重要的是,确定是否可以推断出一种合理的治疗途径,用于治疗内啡肽- mbc疾病。该项目的一个主要优势在于,它涉及到一个成熟的、领先的英国乳腺癌学术研究小组和阿斯利康(Astra Zeneca)的研发肿瘤学iMed小组之间的新合作,阿斯利康是一家领先的全球制药公司,负责开发主要的内分泌疗法,包括芳香化酶抑制剂和抗雌激素,用于乳腺癌。参考文献:Harrod等人,癌基因,2017 http://www.nature.com/onc/journal/vaop/ncurrent/full/onc2016382a.html
英文摘要
Breast cancer is the most common cancer in women Worldwide, with more than 1.5 million cases diagnosed each year. Half a million women die of the disease every year. A critical driver of breast cancer is the hormone estrogen, which works by activating the estrogen receptor protein (ERa). We have used the CRISPR-Cas9 genome editing system to make gene knockins in the well studied and widely used estrogen responsive MCF7 breast cancer cell line to model the major ERa mutations recently identified in treatment-resistant, metastatic breast cancer (EndoR-MBC). These engineered lines are a unique and sophisticated cell resource, which has been made with the purpose of investigating how these mutations act, evaluating their role in metastasis and, importantly, determining if a rationalised route to the treatment can be deduced for the treatment of EndoR-MBC disease. A major strength of this project is that it involves a new collaboration between a well established, leading UK academic breast cancer research group investigating endocrine resistance in breast cancer and the R&D Oncology iMed group at Astra Zeneca, a leading global pharmaceutical company responsible for the development of major endocrine therapies, including aromatase inhibitors and anti-estrogens, for breast cancer.Reference: Harrod et al , Oncogene, 2017 http://www.nature.com/onc/journal/vaop/ncurrent/full/onc2016382a.html
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