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无血清培养的子宫癌肉瘤细胞系中组织多肽抗原的产生

Tissue polypeptide antigen production in a uterine carcinosarcoma cell line in a serum-free culture.

作者信息

Emoto M, Iwasaki H, Kikuchi M, Shirakawa K

机构信息

Department of Obstetrics and Gynecology, Fukuoka University School of Medicine, Japan.

出版信息

Gynecol Oncol. 1996 Mar;60(3):443-9. doi: 10.1006/gyno.1996.0071.

Abstract

Carcinosarcomas (malignant mixed Mullerian tumors, MMMT) of the female genital tract are uncommon neoplasms, most of which show a highly aggressive behavior. However, the biological characteristics of MMMT, especially the producibility of tumor-related substances in vitro, have yet to be clarified. Using a serum-free culture model system which was newly established from an FU-MMT-2 cell line originating from an MMMT of the human uterus, the biological and immunocytochemical characteristics of MMMT cells were examined in vitro. As a control model, the uterine fibroblasts were also cultured in the same conditions. Moreover, several tumor markers were also measured by a radioimmunoassay in the serum of five patients with MMMT. FU-MMT-2 produced and secreted tissue polypeptide antigen (TPA), a tumor marker closely related to the keratin family, under serum-free culture conditions. Moreover, TPA was also immunocytochemically demonstrated in carcinoma cells as well as sarcoma cells in FU-MMT-2. On the other hand, the uterine fibroblasts showed no detectable producibility of the substances examined in vitro. An elevation of the serum TPA levels was also detected in four of five (80%) patients with MMMT. This is the first serum-free culture study of MMMT, which appears to provide a useful model for further studies of the tumor biology in MMMT of the female genital tract. An evaluation of the serum TPA level thus appears to be useful in determining the optimum management of patients with MMMT. In addition, the demonstration of TPA in sarcoma cells of FU-MMT-2 in vitro supports both the theory of a single cell origin and the current concept of MMMT as a "metaplastic carcinoma," as substantiated in our previous study.

摘要

女性生殖道癌肉瘤(恶性米勒管混合瘤,MMMT)是一种罕见的肿瘤,其中大多数具有高度侵袭性。然而,MMMT的生物学特性,尤其是其在体外产生肿瘤相关物质的能力,尚未明确。利用从源自人类子宫MMMT的FU-MMT-2细胞系新建立的无血清培养模型系统,在体外研究了MMMT细胞的生物学和免疫细胞化学特性。作为对照模型,子宫成纤维细胞也在相同条件下培养。此外,还通过放射免疫分析法测定了5例MMMT患者血清中的几种肿瘤标志物。在无血清培养条件下,FU-MMT-2产生并分泌组织多肽抗原(TPA),这是一种与角蛋白家族密切相关的肿瘤标志物。此外,在FU-MMT-2的癌细胞和肉瘤细胞中也通过免疫细胞化学方法证实了TPA的存在。另一方面,子宫成纤维细胞在体外未检测到所研究物质的产生。在5例MMMT患者中,有4例(80%)血清TPA水平升高。这是首次对MMMT进行的无血清培养研究,似乎为进一步研究女性生殖道MMMT的肿瘤生物学提供了一个有用的模型。因此,评估血清TPA水平似乎有助于确定MMMT患者的最佳治疗方案。此外,在体外FU-MMT-2肉瘤细胞中TPA的证实既支持单细胞起源理论,也支持MMMT作为“化生癌”的当前概念,正如我们之前研究所证实的那样。

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