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Cannabinoids Control Breast Cancer Progression Through Id-1

Cannabinoids Control Breast Cancer Progression Through Id-1
大麻素通过 Id-1 控制乳腺癌进展
批准号:
8300959
负责人:
Sean D McAllister
金额:
$33.96万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-28 至 2014-07-31

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项目成果

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中文摘要
翻译
描述(由申请人提供):癌症进展的路径由生长/侵袭和分化的调节机制的改变决定。Id-1蛋白(碱性螺旋-环-螺旋转录因子的抑制剂)的表达已被报道在超过二十种类型的癌症中失调,并且被认为是广泛组织(特别是乳腺)中肿瘤发生和/或转移的关键决定因素。我们对正常和癌性乳腺细胞、小鼠乳腺以及人乳腺癌活检组织中Id-1表达的研究表明,Id-1基因表达与增殖、迁移和侵袭表型相关。因此,降低Id-1表达可能为治疗侵袭性乳腺癌提供合理的治疗策略。我们最近表明,CBD是一种来自大麻的非精神活性大麻素化合物,可以代表第一种可以下调Id-1表达的无毒外源性药物。这种下调以及对人乳腺癌细胞增殖和侵袭力的相应抑制可以为该化合物的抗转移活性提供潜在机制。该提案的目的是确定1)新型CBD类似物通过Id-1下调降低小鼠乳腺癌细胞增殖,侵袭和转移进展的程度,以及2)大麻素化合物抑制Id-1表达的机制。所提出的实验有可能导致开发用于治疗乳腺癌转移的新型化合物。此外,从概述的实验中获得的信息将大大拓宽我们对Id-1和大麻素生物学的知识,因为它与癌症进展有关。了解这些分子事件也可能导致未来开发新的,有效的和无毒的治疗乳腺癌患者。 公共卫生相关性:我们假设,大麻素是一种耐受性良好的化合物,已经用于临床试验,目的与其抗癌活性无关,通过下调Id-1表达和相应的乳腺癌细胞侵袭和转移的能力,对乳腺癌患者有益。使用可以模拟Id-1蛋白在人类肿瘤进展过程中的作用的小鼠模型,我们期望开发新的策略来特异性靶向其表达以用于治疗目的。这项研究可能会导致新的研究领域,用于治疗扩散到身体其他部位的侵袭性乳腺癌,使用新型大麻素化合物,如大麻二酚类似物。
英文摘要
DESCRIPTION (provided by applicant): The path of cancer progression is determined by alterations in the regulatory mechanisms of growth/invasion and differentiation. The expression of Id-1 protein (an inhibitor of basic helix-loop-helix transcription factors) has been reported to be dysregulated in over twenty types of cancer, and suggested as a key determinant of tumorigenesis and/or metastasis in a wide range of tissues, particularly in the breast. Our studies on Id-1 expression in normal and cancerous breast cells, in mouse mammary glands as well as in human breast cancer biopsies, demonstrated that Id-1 gene expression was associated with a proliferative, migratory and invasive phenotype. Reducing Id-1 expression could therefore provide a rational therapeutic strategy for the treatment of aggressive breast cancer. We recently showed that CBD, a non-psychoactive cannabinoid compound derived from cannabis, could represent the first non-toxic exogenous agent that can down-regulate Id-1 expression. This down-regulation, and the corresponding inhibition of human breast cancer cell proliferation and invasiveness, could provide a potential mechanism for the anti-metastatic activity of the compound. The aims of this proposal are to determine 1) the extent to which novel CBD analogs reduce breast cancer cell proliferation, invasion and metastatic progression in mice through Id-1 down-regulation, and 2) the mechanisms behind the inhibition of Id-1 expression by cannabinoid compounds. The proposed experiments have the potential to lead to the development of novel compounds for the treatment of breast cancer metastasis. Additionally, the information gained from the outlined experiments will greatly broaden our knowledge of both Id-1 and cannabinoid biology as it pertains to cancer progression. Understanding these molecular events may also lead to the future development of novel, efficacious and non-toxic treatments for breast cancer patients. PUBLIC HEALTH RELEVANCE: We hypothesize that cannabinoids, well-tolerated compounds that are already being used in clinical trials for purposes unrelated to their anticancer activity, will be of benefit for patients with breast cancers through their ability to down-regulate Id-1 expression and corresponding breast cancer cell invasion and metastasis. Using mouse models that can mimic the role of Id-1 protein during tumor progression in humans, we expect to develop novel strategies to specifically target its expression for therapeutic purposes. This research could lead to new areas of investigation in the treatment of aggressive forms of breast cancer, which spread to other parts of the body, with novel cannabinoid compounds such as analogs of cannabidiol.
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DOI: 10.1007/s11481-015-9608-y
发表时间: 2015-06
期刊: JOURNAL OF NEUROIMMUNE PHARMACOLOGY
影响因子: 6.2
作者: [McAllister, Sean D., Soroceanu, Liliana, Desprez, Pierre-Yves]
通讯作者: Desprez, Pierre-Yves
Cannabinoids Control Breast Cancer Progression Through Id-1
Cannabinoids Control Breast Cancer Progression Through Id-1
Control of Breast Cancer by the Endocannabinoid System
Control of Breast Cancer by the Endocannabinoid System
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