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原发性嗅神经母细胞瘤中的8号染色体三体。

Trisomy 8 in primary esthesioneuroblastoma.

作者信息

VanDevanter D R, George D, McNutt M A, Vogel A, Luthardt F

机构信息

Clinical Research Division, Swedish Hospital Medical Center, Seattle, WA 98104.

出版信息

Cancer Genet Cytogenet. 1991 Nov;57(1):133-6. doi: 10.1016/0165-4608(91)90198-4.

Abstract

Esthesioneuroblastoma is a rare malignancy believed to be derived from neuroectodermal stem cells within the olfactory epithelium. We have obtained the karyotype of a primary esthesioneuroblastoma following brief (7-day) in vitro culture, and have determined that the only observable cytogenetic anomaly is the presence of an additional chromosome 8. Previously, the karyotypes of two cell lines established from metastatic esthesioneuroblastomas have been reported to contain the equivalent of three copies of chromosome 8, in addition to other chromosomal aberrations, including the reciprocal translocation, t(11;22)(q24;q12). Examination of the cytogenetic literature suggests that an extra copy of chromosome 8 is a common occurrence in undifferentiated small round cell tumors frequently observed to carry the t(11;22), including esthesioneuroblastoma, Ewing's sarcoma, peripheral neuroepithelioma, Askin's tumor, and rhabdomyosarcoma. These data, combined with our report of a small round cell tumor with the karyotype 47,XY, +8, indicate that trisomy 8 may be a common phenomenon in these tumors, and may also provide some sort of selective advantage to these tumor types.

摘要

嗅神经母细胞瘤是一种罕见的恶性肿瘤,被认为起源于嗅上皮内的神经外胚层干细胞。我们在短期(7天)体外培养后获得了一例原发性嗅神经母细胞瘤的核型,并确定唯一可观察到的细胞遗传学异常是额外出现了一条8号染色体。此前,据报道,从转移性嗅神经母细胞瘤建立的两个细胞系的核型除了包含其他染色体畸变,包括相互易位t(11;22)(q24;q12)外,还含有相当于三条8号染色体的拷贝。对细胞遗传学文献的研究表明,额外的一条8号染色体在经常观察到携带t(11;22)的未分化小细胞肿瘤中很常见,包括嗅神经母细胞瘤、尤因肉瘤、外周神经上皮瘤、阿金氏瘤和横纹肌肉瘤。这些数据,再加上我们关于一例核型为47,XY, +8的小细胞肿瘤的报告,表明8号染色体三体可能是这些肿瘤中的常见现象,并且可能也为这些肿瘤类型提供了某种选择性优势。

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