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化学诱导和自发产生的小鼠肺泡源性癌的细胞培养模型

A cell culture model of chemically and spontaneously derived mouse lung alveologenic carcinoma.

作者信息

Smith G J, Steele J G, Bentel J M, Loo C K

机构信息

Carcinogenesis Research Unit, School of Pathology, University of New South Wales, Australia.

出版信息

Cell Biol Toxicol. 1988 Sep;4(3):333-48. doi: 10.1007/BF00058741.

Abstract

Malignant cell lines related to mouse lung alveologenic carcinoma have been established from urethane-induced tumors and after in vitro spontaneous transformation of preneoplastic cell lines. Both the chemically and spontaneously transformed cell lines formed invasive, poorly differentiated carcinomas with secondary lung deposits when implanted subcutaneously in immune-suppressed mice. They differed from the related preneoplastic cell line in coordinately exhibiting anchorage-independent growth, reduced epidermal growth factor receptor activity and absence of pericellular fibronectin. These data suggest that similar molecular events may occur in type 2 pneumocyte-related cells in order to generate mouse lung alveologenic adenomas and carcinomas by both spontaneous and chemical carcinogen induction mechanisms. A reduced level of pericellular fibronectin was also demonstrated in an in situ compressive urethane-induced mouse lung adenoma. Loss of pericellular fibronectin may therefore be an early and persistent phenotypic alteration during transformation to the alveologenic adenoma and carcinoma.

摘要

与小鼠肺泡源性癌相关的恶性细胞系已从氨基甲酸乙酯诱导的肿瘤以及肿瘤前细胞系的体外自发转化中建立。当将化学转化和自发转化的细胞系皮下植入免疫抑制小鼠体内时,它们都会形成具有肺继发性沉积物的侵袭性、低分化癌。它们与相关的肿瘤前细胞系不同,表现为协同呈现不依赖贴壁生长、表皮生长因子受体活性降低以及细胞周围纤连蛋白缺失。这些数据表明,在2型肺细胞相关细胞中可能发生类似的分子事件,以便通过自发和化学致癌物诱导机制产生小鼠肺泡源性腺瘤和癌。在原位压缩氨基甲酸乙酯诱导的小鼠肺腺瘤中也证实了细胞周围纤连蛋白水平降低。因此,细胞周围纤连蛋白的缺失可能是向肺泡源性腺瘤和癌转化过程中的一种早期且持续的表型改变。

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