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经体内组织学分化改变后建立的人卵巢癌肉瘤细胞系的特性分析

Characterization of a human carcinosarcoma cell line of the ovary established after in vivo change of histologic differentiation.

作者信息

Möbus V J, Gerharz C D, Weikel W, Merk O, Dreher L, Kreienberg R, Moll R

机构信息

Department of Obstetrics and Gynecology, Städtische Kliniken Frankfurt a.M., Frankfurt, Germany.

出版信息

Gynecol Oncol. 2001 Dec;83(3):523-32. doi: 10.1006/gyno.2001.6425.

Abstract

OBJECTIVES

Cell lines are valuable in vitro models for clinical and basic research. Most ovarian cancer cell lines described are serous cystadenocarcinomas or poorly differentiated adenocarcinomas. The establishment of ovarian cancer cell lines with rare histologic differentiation is especially of interest. We describe the establishment of a carcinosarcoma cell line of the ovary after in vivo selection.

METHODS

The cell line OV-MZ-22 was established from a solid tumor mass in the upper abdomen. At the time of establishment, the patient underwent secondary debulking and was pretreated with six cycles of cis-platinum/epirubicin/cyclophosphamide. Features of the cell line studied included morphology, ultrastructure, heterotransplantation, chromosome analysis, and analysis of intermediate filament proteins and actins by immunocytochemistry.

RESULTS

The first histologic report of the patient described a papillary cystadenocarcinoma, which changed to a carcinosarcoma with predominantly sarcomatous differentiation at secondary debulking. This cell line is aneuploid and shows no expression of the tumor-associated antigens CA-125 and CEA, but an overexpression of MDR-1, lung resistance protein, p53, and topoisomerase I and II, but not of multidrug-resistance-associated protein. The cell line did not give rise to transplant tumors in nude mice. The histologic and immunocytochemical comparison of the primary and the relapsed tumor proved evidence of an in vivo change of differentiation from predominantly papillary cystadenocarcinoma to carcinosarcoma. Morphological characteristics and intermediate filament pattern underlined the sarcomatous differentiation and origin of this cell line. The differentiation phenotype of OV-MZ-22 cells is that of smooth-muscle cells.

CONCLUSION

The change of histologic differentiation was apparently due to a selection process caused by platinum-containing chemotherapy. The origin of the cell line and its rarity make this new line an appropriate tool for further investigation.

摘要

目的

细胞系是临床和基础研究中很有价值的体外模型。所描述的大多数卵巢癌细胞系为浆液性囊腺癌或低分化腺癌。建立具有罕见组织学分化的卵巢癌细胞系尤其令人感兴趣。我们描述了经体内筛选后建立的一种卵巢癌肉瘤细胞系。

方法

OV-MZ-22细胞系由上腹部实性肿块建立。建立时,患者接受了二次肿瘤细胞减灭术,并接受了六个周期的顺铂/表柔比星/环磷酰胺预处理。对该细胞系的研究特征包括形态学、超微结构、异种移植、染色体分析以及通过免疫细胞化学分析中间丝蛋白和肌动蛋白。

结果

患者的首次组织学报告描述为乳头状囊腺癌,在二次肿瘤细胞减灭术时变为以肉瘤样分化为主的癌肉瘤。该细胞系为非整倍体,未显示肿瘤相关抗原CA-125和癌胚抗原的表达,但多药耐药蛋白1、肺耐药蛋白、p53以及拓扑异构酶I和II过表达,而多药耐药相关蛋白未过表达。该细胞系在裸鼠中未形成移植瘤。原发肿瘤和复发肿瘤的组织学及免疫细胞化学比较证明了在体内从主要为乳头状囊腺癌向癌肉瘤的分化改变。形态学特征和中间丝模式强调了该细胞系的肉瘤样分化及其起源。OV-MZ-22细胞的分化表型为平滑肌细胞的表型。

结论

组织学分化的改变显然是由含铂化疗引起的选择过程所致。该细胞系的起源及其稀有性使其成为进一步研究的合适工具。

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