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Establishment and Characterization of a Small Round Cell Sarcoma Cell Line SCCH‐196 with t(11;22)(q24;q12)

机译:t(11; 22)(q24; q12)的小圆形细胞肉瘤细胞系SCCH-196的建立和表征

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摘要

A cell line designated SCCH‐196 was established from an extraskeletal small round cell sarcoma developed in a 16‐year‐old Japanese girl. The cells grew as a monolayer, and have been continuously propagated by serial subcultures during the past 26 months. Cells from the primary tumor and those from the SCCH‐196 cell line at passage 10 both showed the same karyotype, 51, XX, + 8, + 20, + 21, t(11;22)(q24;q12), + i(1q), + i(1q). Histologically the primary tumor was difficult to classify as either Ewing's sarcoma (ES) or peripheral neuroepithelioma (NE). Neuron‐specific enolase‐positive cells in the primary tumor and the occurrence in the upper extremity were in favor of NE, while positive reaction of SCCH‐196 cells to an ES‐speciflc monoclonal antibody 5C11 suggested a diagnosis of ES. The SCCH‐196 cell line may be useful for basic studies on differentiation of neuroectodermal tumors, and for future cloning of still unidentified genes which may be located at the breakpoints of the 11;22 translocation.
机译:从一名16岁日本女孩体内发育的骨骼外小圆形细胞肉瘤建立了一个名为SCCH-196的细胞系。细胞以单层生长,并在过去26个月中通过连续传代培养连续繁殖。来自第10代的原发性肿瘤细胞和SCCH-196细胞系的细胞均显示相同的核型,即51,XX,+ 8,+ 20,+ 21,t(11; 22)(q24; q12),+ i (1q),+ i(1q)。从组织学上讲,原发肿瘤很难归类为尤因肉瘤(ES)或周围神经上皮瘤(NE)。原发性肿瘤中神经元特异性烯醇化酶阳性细胞和上肢的发生均支持NE,而SCCH-196细胞对ES特异性单克隆抗体5C11的阳性反应则提示诊断为ES。 SCCH-196细胞系可用于神经外胚层肿瘤分化的基础研究,以及将来克隆可能位于11; 22易位断点的尚不清楚的基因。

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