Hakozaki Michiyuki, Tamura Hirosumi, Dobashi Yuu, Yoshida Aki, Kato Kouki, Tajino Takahiro, Yamada Hitoshi, Kaneuchi Yoichi, Katahira Kiyoaki, Ezaki Junji, Waguri Satoshi, Konno Shinichi, Watanabe Shinya
Medical-Industrial Translational Research Center, Fukushima Global Medical Science Center, Fukushima Medical University, Fukushima, Japan
Department of Orthopaedic Surgery, Fukushima Medical University School of Medicine, Fukushima, Japan.
Anticancer Res. 2018 Sep;38(9):5035-5042. doi: 10.21873/anticanres.12822.
BACKGROUND/AIM: Clear cell sarcoma (CCS) of soft tissue is exceedingly rare and frequently exhibits aggressive behavior. Toward the goals of improving the aggressive course and poor prognosis of CCS, and establish new therapeutic methods, molecular genetic and biological characterizations of CCS are required.
A new human CCS cell line (designated RSAR001) was established from the pleural effusion of a 44-year-old man with multiple lung metastases and pleural dissemination. The cell line and its xenograft were characterized including their morphology, immunohistochemistry, cytogenetic analysis, reverse transcription-polymerase chain reaction, direct sequencing analysis, and fluorescence in situ hybridization analysis.
The cell line has been maintained for over 12 months with more than 50 passages. RSAR001 cells exhibited a fascicular or diffuse growth pattern of short spindle- or oval-shaped cells with clear cytoplasm in heterotransplanted tumor, that was similar to the primary tumor. Immunophenotypically, RSAR001 cells in vitro and in vivo exhibited almost the same characteristics as the primary tumor. Cytogenetic analyses revealed a translocation, t(12;22)(q13;q12). Reverse transcription-polymerase chain reaction and direct sequencing analysis detected transcripts of the Ewing sarcoma breakpoint region 1-activating transcription factor 1 (EWSR1-ATF1) type 1 fusion gene. Fluorescence in situ hybridization using a break-apart probe for the EWSR1 gene on 22q12 showed a rearrangement.
These findings indicate that the RSAR001 cell line harbors EWSR1-ATF1 type 1 chimeric fusion gene, which is specific to CCS. RSAR001 cells might be useful for investigating biological behaviors and developing new treatments such as molecular-targeting antitumor drugs or immunological drugs for CCS.
背景/目的:软组织透明细胞肉瘤(CCS)极为罕见,且常表现出侵袭性行为。为改善CCS的侵袭性病程和不良预后,并建立新的治疗方法,需要对CCS进行分子遗传学和生物学特征分析。
从一名44岁患有多处肺转移和胸膜播散的男性胸腔积液中建立了一种新的人CCS细胞系(命名为RSAR001)。对该细胞系及其异种移植瘤进行了特征分析,包括形态学、免疫组织化学、细胞遗传学分析、逆转录-聚合酶链反应、直接测序分析和荧光原位杂交分析。
该细胞系已传代50多次,维持了12个月以上。RSAR001细胞在异种移植瘤中呈现短梭形或椭圆形细胞的束状或弥漫性生长模式,细胞质清晰,与原发肿瘤相似。免疫表型分析显示,RSAR001细胞在体外和体内表现出与原发肿瘤几乎相同的特征。细胞遗传学分析发现了一种易位,t(12;22)(q13;q12)。逆转录-聚合酶链反应和直接测序分析检测到尤文肉瘤断点区域1-激活转录因子1(EWSR1-ATF1)1型融合基因的转录本。使用针对22q12上EWSR1基因的断裂探针进行荧光原位杂交显示有重排。
这些发现表明,RSAR001细胞系含有EWSR1-ATF1 1型嵌合融合基因,这是CCS所特有的。RSAR001细胞可能有助于研究CCS的生物学行为,并开发新的治疗方法,如分子靶向抗肿瘤药物或免疫药物。