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细胞遗传学异常在未经培养的前列腺癌细胞中很常见。

Cytogenetic abnormalities are frequent in uncultured prostate cancer cells.

作者信息

Webb H D, Hawkins A L, Griffin C A

机构信息

Department of Pathology, Johns Hopkins University, Baltimore, Maryland, USA.

出版信息

Cancer Genet Cytogenet. 1996 Jun;88(2):126-32. doi: 10.1016/0165-4608(95)00305-3.

Abstract

Despite attempts by several laboratories to identify consistent chromosome abnormalities in cancer of the prostate, relatively few clonal changes have been found. We compared analysis of metaphases from uncultured specimens of primary prostate cancer (direct preparations) with those obtained from short-term culture using various media. While the number of metaphases in uncultured specimens was low, and chromosome morphology fair to poor, structural chromosome changes could be identified as clonal in 5 of 14 specimens (36%). In contrast, while clonal abnormalities were found in 20 of 61 (33%) specimens analyzed after short-term culture, these abnormalities were predominantly numerical and simple structural changes. Two tumors metastatic to lymph nodes were studied using direct preparations; both were near tetraploid, with multiple structural abnormalities, including isochromosome 8q in both and del(8)(p21) in one. Cytogenetic analyses of metastatic prostate tumors have been very limited, and these data suggest that formation of an i(8q) may be the mechanism by which loss of heterozygosity of 8p, reported frequently in molecular analyses, occurs. Our findings indicate that prostate cancers, like most solid tumors, do have clonal chromosome abnormalities that are frequently complex, but the method that reproducibly yields representative karyotypes from this particular tumor remains to be identified.

摘要

尽管多个实验室试图鉴定前列腺癌中一致的染色体异常,但发现的克隆性改变相对较少。我们将原发性前列腺癌未培养标本(直接制片)的中期分析与使用各种培养基进行短期培养获得的中期分析进行了比较。虽然未培养标本中的中期相数量较少,染色体形态中等至较差,但在14个标本中的5个(36%)中可将染色体结构改变鉴定为克隆性的。相比之下,虽然在短期培养后分析的61个标本中的20个(33%)中发现了克隆性异常,但这些异常主要是数目和简单的结构改变。使用直接制片法研究了两个转移至淋巴结的肿瘤;两者均接近四倍体,有多个结构异常,包括两者均有8号染色体长臂等臂染色体,其中一个有8号染色体短臂缺失(8p21)。转移性前列腺肿瘤的细胞遗传学分析非常有限,这些数据表明形成8号染色体长臂等臂染色体(i(8q))可能是分子分析中经常报道的8号染色体短臂杂合性缺失发生的机制。我们的研究结果表明,与大多数实体瘤一样,前列腺癌确实存在经常复杂的克隆性染色体异常,但从这种特定肿瘤中可重复产生代表性核型的方法仍有待确定。

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