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1
A Case Report of a Malignant Fibrous Histiocytoma in a T-cell Receptor β Chain and p53 Double-knockout Mouse.T细胞受体β链和p53双敲除小鼠发生恶性纤维组织细胞瘤的病例报告
J Toxicol Pathol. 2011 Dec;24(4):251-5. doi: 10.1293/tox.24.251. Epub 2012 Jan 7.
2
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Intestinal microflora are necessary for development of spontaneous adenocarcinoma of the large intestine in T-cell receptor beta chain and p53 double-knockout mice.肠道微生物群对于T细胞受体β链和p53双敲除小鼠自发性大肠腺癌的发展是必需的。
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Systemic deficits in transporter for antigen presentation (TAP)-1 or proteasome subunit LMP2 have little or no effect on tumor incidence.抗原呈递转运体(TAP)-1或蛋白酶体亚基LMP2的系统性缺陷对肿瘤发生率几乎没有影响。
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p53, the cellular gatekeeper for growth and division.p53,细胞生长和分裂的守门人。
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T-cell alpha beta + and gamma delta + deficient mice display abnormal but distinct phenotypes toward a natural, widespread infection of the intestinal epithelium.T细胞αβ +和γδ +缺陷小鼠对肠道上皮的自然广泛感染表现出异常但不同的表型。
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Spontaneous and carcinogen-induced tumorigenesis in p53-deficient mice.p53基因缺陷小鼠的自发及致癌物诱导的肿瘤发生
Nat Genet. 1993 Nov;5(3):225-9. doi: 10.1038/ng1193-225.
9
Spontaneous development of inflammatory bowel disease in T cell receptor mutant mice.T细胞受体突变小鼠中炎症性肠病的自发发展。
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Mutations in the p53 tumor suppressor gene: clues to cancer etiology and molecular pathogenesis.p53肿瘤抑制基因的突变:癌症病因学和分子发病机制的线索
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T细胞受体β链和p53双敲除小鼠发生恶性纤维组织细胞瘤的病例报告

A Case Report of a Malignant Fibrous Histiocytoma in a T-cell Receptor β Chain and p53 Double-knockout Mouse.

作者信息

Ando Minoru, Kado Shoichi, Suzuki Tomo, Yamamoto Ryota, Nagata Yuriko, Hata Chie, Uchida Kazumi, Kaneko Kimiyuki

机构信息

Yakult Central Institute for Microbiological Research, 1796 Yaho, Kunitachi-shi, Tokyo 186-8650, Japan.

出版信息

J Toxicol Pathol. 2011 Dec;24(4):251-5. doi: 10.1293/tox.24.251. Epub 2012 Jan 7.

DOI:10.1293/tox.24.251
PMID:22319239
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3266362/
Abstract

A subcutaneous tumor was found in the right abdomen of a 16-week-old male TCRβ and p53 double-knockout mouse. The tumor had indistinct borders with the surrounding tissue. The cut surface after formalin fixation was pale yellowish white, partially dark red and partly white. Histologically, the tumor was composed of three distinct regions. The first region showed pleomorphic cells arranged in sheets. The second region showed spindle cells arranged in interlacing fascicles. The final region contained a mixture of the above mentioned two types of cells. Furthermore, a small amount of collagen fibers, round cells, multinucleated giant cells, and cells with eosinophilic granules were observed between these tumor cells. Immunohistochemical examination and electron microscopy identified that the pleomorphic cells and spindle cells were histiocytes and fibroblasts, respectively, and that the round cells were undifferentiated mesenchymal cells. Based on these findings, the tumor was diagnosed as a malignant fibrous histiocytoma.

摘要

在一只16周龄的雄性TCRβ和p53双敲除小鼠的右腹部发现了一个皮下肿瘤。该肿瘤与周围组织边界不清。福尔马林固定后的切面为淡黄色白色,部分暗红色,部分白色。组织学上,肿瘤由三个不同区域组成。第一个区域显示多形性细胞呈片状排列。第二个区域显示梭形细胞呈交织束状排列。最后一个区域包含上述两种类型细胞的混合物。此外,在这些肿瘤细胞之间观察到少量胶原纤维、圆形细胞、多核巨细胞和嗜酸性颗粒细胞。免疫组织化学检查和电子显微镜鉴定多形性细胞和梭形细胞分别为组织细胞和成纤维细胞,圆形细胞为未分化间充质细胞。基于这些发现,该肿瘤被诊断为恶性纤维组织细胞瘤。