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在免疫功能正常的小鼠中,构建由同源性 Trp53 改变和 Pten 缺失驱动的侵袭性前列腺癌模型。

Modelling aggressive prostate cancers of young men in immune-competent mice, driven by isogenic Trp53 alterations and Pten loss.

机构信息

Peter MacCallum Cancer Centre, 305 Grattan St, Melbourne, VIC, 3000, Australia.

Sir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville, VIC, 3010, Australia.

出版信息

Cell Death Dis. 2022 Sep 8;13(9):777. doi: 10.1038/s41419-022-05211-y.

Abstract

Understanding prostate cancer onset and progression in order to rationally treat this disease has been critically limited by a dire lack of relevant pre-clinical animal models. We have generated a set of genetically engineered mice that mimic human prostate cancer, initiated from the gland epithelia. We chose driver gene mutations that are specifically relevant to cancers of young men, where aggressive disease poses accentuated survival risks. An outstanding advantage of our models are their intact repertoires of immune cells. These mice provide invaluable insight into the importance of immune responses in prostate cancer and offer scope for studying treatments, including immunotherapies. Our prostate cancer models strongly support the role of tumour suppressor p53 in functioning to critically restrain the emergence of cancer pathways that drive cell cycle progression; alter metabolism and vasculature to fuel tumour growth; and mediate epithelial to mesenchymal-transition, as vital to invasion. Importantly, we also discovered that the type of p53 alteration dictates the specific immune cell profiles most significantly disrupted, in a temporal manner, with ramifications for disease progression. These new orthotopic mouse models demonstrate that each of the isogenic hotspot p53 amino acid mutations studied (R172H and R245W, the mouse equivalents of human R175H and R248W respectively), drive unique cellular changes affecting pathways of proliferation and immunity. Our findings support the hypothesis that individual p53 mutations confer their own particular oncogenic gain of function in prostate cancer.

摘要

为了合理治疗前列腺癌,深入了解其发病机制和进展受到严重限制,因为缺乏相关的临床前动物模型。我们构建了一组遗传工程小鼠,模拟了源自前列腺上皮的人类前列腺癌。我们选择了与年轻男性癌症特别相关的驱动基因突变,因为侵袭性疾病会带来更大的生存风险。我们模型的一个突出优势是其完整的免疫细胞库。这些小鼠为研究免疫反应在前列腺癌中的重要性提供了宝贵的见解,并为研究治疗方法(包括免疫疗法)提供了可能。我们的前列腺癌模型强烈支持肿瘤抑制因子 p53 的作用,它可以严格抑制驱动细胞周期进程的癌症途径的出现;改变代谢和血管以滋养肿瘤生长;并介导上皮到间充质的转化,这对侵袭至关重要。重要的是,我们还发现,p53 改变的类型以时间依赖的方式显著破坏了特定的免疫细胞谱,这对疾病进展有影响。这些新的原位小鼠模型表明,研究的每个同型热点 p53 氨基酸突变(R172H 和 R245W,分别对应人类的 R175H 和 R248W)都驱动了独特的细胞变化,影响了增殖和免疫途径。我们的研究结果支持这样一种假设,即单个 p53 突变赋予了前列腺癌特有的致癌功能获得。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ff4/9465983/1ab0e32685b9/41419_2022_5211_Fig1_HTML.jpg

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