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猫乳腺肿瘤中基质(myofibroblast)和成纤维细胞黏附分子(tenascin-C)的形态和分布。

Appearance and distribution of stromal myofibroblasts and tenascin-C in feline mammary tumors.

机构信息

Department of Veterinary Pathology, Faculty of Veterinary Medicine, Nippon Veterinary and Life Science University, Tokyo, Japan.

出版信息

Histol Histopathol. 2011 Mar;26(3):297-305. doi: 10.14670/HH-26.297.

Abstract

Myofibroblasts and extracellular matrix protein tenascin-C (Tn-C) are known to be implicated in cancer progression in human cancer. In feline mammary tumors that are a suitable model for human breast cancer, however, little is known about stromal myofibroblasts and no information is available on the expression of Tn-C. Feline samples of normal mammary glands and proliferating mammary lesions were routinely processed and serial sections were cut and immunostained with anti-α-smooth muscle actin (α-SMA) or Tn-C antibody. Myofibroblasts were not included in the stroma of 90% (9/10) of normal mammary gland tissues, 92% (12/13) of adenosis, and 63% (5/8) of simple adenomas. On the other hand, all 40 simple carcinomas contained stromal myofibroblasts to a varied extent. Tn-C expression was detected in the stroma of 92% (37/40) of carcinomas, and its global distribution almost coincided with that of myofibroblasts. In addition, Tn-C immunoreactivity was occasionally observed in the basement membrane zone around ducts in some cases of normal mammary glands and benign lesions, but barely observed in the stroma. These results suggest that stromal myofibroblasts may be a major cellular source of Tn-C and be involved in malignant progression of feline mammary tumor.

摘要

肌成纤维细胞和细胞外基质蛋白 tenascin-C(Tn-C)已知与人类癌症的癌症进展有关。然而,在猫的乳腺肿瘤中,这种肿瘤是人类乳腺癌的合适模型,对于基质肌成纤维细胞知之甚少,并且关于 Tn-C 的表达也没有信息。对正常乳腺组织和增生性乳腺病变的猫样本进行了常规处理,并对其进行连续切片,用抗α-平滑肌肌动蛋白(α-SMA)或 Tn-C 抗体进行免疫染色。在 90%(9/10)的正常乳腺组织、92%(12/13)的腺病和 63%(5/8)的单纯腺瘤中,肌成纤维细胞不包含在基质中。另一方面,所有 40 个单纯癌均不同程度地含有基质肌成纤维细胞。在 92%(37/40)的癌中检测到 Tn-C 在基质中的表达,其整体分布几乎与肌成纤维细胞的分布一致。此外,在一些正常乳腺和良性病变的导管周围基底膜区偶尔观察到 Tn-C 免疫反应性,但在基质中几乎观察不到。这些结果表明,基质肌成纤维细胞可能是 Tn-C 的主要细胞来源,并参与猫乳腺肿瘤的恶性进展。

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