TRP53 (p53)的缺失加速了SJL/J小鼠的肿瘤发生,改变了肿瘤谱。

Q2 Biochemistry, Genetics and Molecular Biology
Jane A Branca, Benjamin E Low, Ruth L Saxl, Jennifer K Sargent, Rosalinda A Doty, Michael V Wiles, Beth L Dumont, Muneer G Hasham
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引用次数: 1

摘要

作为基因组的守护者,转化相关蛋白53 (TRP53)是一种众所周知的肿瘤抑制因子。在这里,我们描述了一种新的TRP53缺陷小鼠模型- sjl /J小鼠的肿瘤易发背景。TRP53的缺失(TRP53无合子性)导致肿瘤谱从非霍奇金样疾病转变为胸腺淋巴瘤和睾丸畸胎瘤,发病速度非常快,平均约为12周龄。在单倍型研究中,我们比较了肿瘤易发和肿瘤耐药的Trp53缺失小鼠品系,发现其他肿瘤抑制基因、DNA修复和/或免疫系统基因可以调节Trp53缺失品系的肿瘤发生率,这表明即使是Trp53这样的强肿瘤抑制基因也会受到遗传背景的调节。由于SJL/J TRP53缺失小鼠的肿瘤发展速度较快,因此本研究产生的SJL/J TRP53缺失小鼠可作为高效的化疗或免疫治疗筛选小鼠模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Loss of TRP53 (p53) accelerates tumorigenesis and changes the tumor spectrum of SJL/J mice.

Loss of TRP53 (p53) accelerates tumorigenesis and changes the tumor spectrum of SJL/J mice.

Loss of TRP53 (p53) accelerates tumorigenesis and changes the tumor spectrum of SJL/J mice.

Loss of TRP53 (p53) accelerates tumorigenesis and changes the tumor spectrum of SJL/J mice.

Known as the guardian of the genome, transformation-related protein 53 (TRP53) is a well -known tumor suppressor. Here, we describe a novel TRP53 deficient mouse model on a tumor prone background-SJL/J mice. The absence of TRP53 (TRP53 nullizygosity) leads to a shift in the tumor spectrum from a non-Hodgkin's-like disease to thymic lymphomas and testicular teratomas at a very rapid tumor onset averaging ~12 weeks of age. In haplotype studies, comparing tumor prone versus tumor resistant Trp53 null mouse strains, we found that other tumor suppressor, DNA repair and/or immune system genes modulate tumor incidence in TRP53 null strains, suggesting that even a strong tumor suppressor such as TRP53 is modulated by genetic background. Due to their rapid development of tumors, the SJL/J TRP53 null mice generated here can be used as an efficient chemotherapy or immunotherapy screening mouse model.

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来源期刊
Genes and Cancer
Genes and Cancer Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.90
自引率
0.00%
发文量
6
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