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神经母细胞瘤中11号染色体及14q序列的缺失

Deletion of chromosome 11 and of 14q sequences in neuroblastoma.

作者信息

Srivatsan E S, Ying K L, Seeger R C

机构信息

Division of Hematology-Oncology, Childrens Hospital Los Angeles, CA 90027.

出版信息

Genes Chromosomes Cancer. 1993 May;7(1):32-7. doi: 10.1002/gcc.2870070106.

Abstract

Restriction fragment length polymorphism (RFLP) analysis carried out on 45 primary neuroblastomas showed deletion of chromosome 11 sequences in 12 of 37 (32%) informative cases. Both 11p and 11q probes were informative in seven tumors; loss of all of chromosome 11, of only 11p sequences, and of only 11q sequences was observed in 4, 1, and 2 tumors, respectively. A cytogenetic abnormality involving translocation of chromosome arm 11q to chromosome arm 1p was observed in a primary tumor. Deletion of 14q was observed in 6 of 27 (22%) informative cases. Deletion of chromosome 11 but not 14q may correlate with regional and metastatic disease. These results suggest a possible role for sequences localized to chromosome 11 and to 14q in the development and/or progression of neuroblastoma.

摘要

对45例原发性神经母细胞瘤进行的限制性片段长度多态性(RFLP)分析显示,在37例(32%)信息丰富的病例中,有12例存在11号染色体序列缺失。11p和11q探针在7例肿瘤中能提供信息;分别在4例、1例和2例肿瘤中观察到11号染色体全部缺失、仅11p序列缺失以及仅11q序列缺失。在1例原发性肿瘤中观察到涉及11号染色体长臂易位至1号染色体长臂的细胞遗传学异常。在27例(22%)信息丰富的病例中,有6例观察到14号染色体长臂缺失。11号染色体缺失但14号染色体长臂未缺失可能与局部和转移性疾病相关。这些结果表明定位于11号染色体和14号染色体长臂的序列在神经母细胞瘤的发生和/或进展中可能起作用。

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