Yonamine K, Hayashi K, Iida T
Department of Obstetrics and Gynecology, St. Marianna University.
Hum Cell. 1999 Sep;12(3):139-48.
A novel cell line derived from a surgically resected ovarian clear cell adenocarcinoma of 46 year-old Japanese woman was established and designated SMOV-2. Cells of this lineage were continuously propagated in vitro over 44 months and were grown in a mono-layered sheet with a doubling time of 48.2 hours. The histopathology of the transplanted tumor in nude mice showed two distinctive cell types, hobnail cells and clear cells, which demonstrated recognizable characteristics of clear cell adenocarcinoma, as compared to resected original tumors. At the molecular level, SMOV-2 cells had the wild type p53 genes that were free from missence mutations. Anticancer agents (cisplatin and paclitaxel) were examined for cytotoxity against these SMOV-2 cells in vitro. These examinations revealed that the chemotherapy-treated cells had decreased proliferation, cell cycle arrests, and induction of apoptosis by the anticancer agents. As can be gleaned from this research, SMOV-2 is a valuable model to study the mechanism of apoptotic responses of solid tumors to future anticancer agents.
从一名46岁日本女性手术切除的卵巢透明细胞腺癌中建立了一种新的细胞系,并命名为SMOV-2。该细胞系的细胞在体外连续传代44个月,以单层培养,倍增时间为48.2小时。裸鼠移植瘤的组织病理学显示出两种不同的细胞类型,鞋钉样细胞和透明细胞,与切除的原发肿瘤相比,表现出透明细胞腺癌可识别的特征。在分子水平上,SMOV-2细胞具有野生型p53基因,无错义突变。检测了抗癌药物(顺铂和紫杉醇)对这些SMOV-2细胞的体外细胞毒性。这些检测表明,经化疗处理的细胞增殖减少、细胞周期停滞,并被抗癌药物诱导凋亡。从这项研究可以看出,SMOV-2是研究实体瘤对未来抗癌药物凋亡反应机制的有价值模型。