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[DNA水平上的癌症诊断]

[Diagnosis of cancer at the DNA level].

作者信息

Kawa-Ha K, Yabuuchi H

机构信息

Dept. of Pediatrics, Osaka University Hospital.

出版信息

Gan To Kagaku Ryoho. 1988 Sep;15(9):2667-74.

PMID:3166365
Abstract

Recent recombinant DNA techniques have made possible the production of gene probes and the search for genetic damage in neoplastic cells, and now occupy one of the central place in cancer research. More recently, detection of immunoglobulin and T cell receptor gene rearrangements has been shown to be a powerful procedure for identifying monoclonality and the cellular lineage of lymphoid cells even when conventional studies give an ambiguous diagnosis. Such genetic markers are not only useful for differential diagnosis and classification, but serves also as a sensitive unique clonal marker to detect early cancer relapse. In a similar manner, chromosomal translocations associated with specific disease types can be detected with DNA probes in southern blot analysis without the use of conventional cytogenetics. These methods have wider application and will play an increasing role in the clinical use in the near future.

摘要

最近,重组DNA技术使得基因探针的生产以及对肿瘤细胞中基因损伤的研究成为可能,并且目前在癌症研究中占据核心地位之一。最近,免疫球蛋白和T细胞受体基因重排的检测已被证明是一种强大的方法,即使在传统研究给出模糊诊断的情况下,也能用于识别淋巴细胞的单克隆性和细胞谱系。此类基因标记不仅有助于鉴别诊断和分类,还可作为检测癌症早期复发的敏感独特的克隆标记。以类似的方式,通过Southern印迹分析中的DNA探针可以检测与特定疾病类型相关的染色体易位,而无需使用传统的细胞遗传学方法。这些方法具有更广泛的应用,并且在不久的将来将在临床应用中发挥越来越重要的作用。

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