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用于癌症和遗传研究、诊断及预后的中期和间期细胞的分子细胞遗传学。在组织切片和细胞悬液中的应用。

Molecular cytogenetics in metaphase and interphase cells for cancer and genetic research, diagnosis and prognosis. Application in tissue sections and cell suspensions.

作者信息

Mühlmann Maria

机构信息

Comisión Nacional de Energía Atómica (CNEA), Consejo Nacional de Ciencia y Tecnología (CONICET), Buenos Aires, Argentina.

出版信息

Genet Mol Res. 2002 Jun 30;1(2):117-27.

Abstract

As the pioneer among molecular cytogenetics techniques, fluorescence in situ hybridization (FISH) allows identification of specific sequences in a structurally preserved cell, in metaphase or interphase. This technique, based on the complementary double-stranded nature of DNA, hybridizes labeled specific DNA (probe). The probe, bound to the target, will be developed into a fluorescent signal. The fact that the signal can be detected clearly, even when fixed in interphase, improves the accuracy of the results, since in some cases it is extremely difficult to obtain mitotic samples. FISH is still used mostly in research, but there are diagnostic applications. New nomenclature is being developed in order to define many of the aberrations that were not distinguished before FISH. Prenatal diagnosis of aneuploidies and malignancies are promptly detected with FISH, which is very useful in critical cases. In some tumors, where chromosomal abnormalities are too complicated to classify manually, the technique of comparative genomic hybridization (CGH), a competitive FISH, allows examiners to determine complete or partial gain or loss of chromosomes. CGH results allow the classification of many tumor cell lines and along with other complementary techniques, like microdissection-FISH, PRINS, etc., increase the possibility of choosing an appropriate treatment for cancer patients.

摘要

作为分子细胞遗传学技术中的先驱,荧光原位杂交(FISH)可在中期或间期的结构完整细胞中鉴定特定序列。该技术基于DNA的互补双链性质,使标记的特定DNA(探针)进行杂交。与靶标结合的探针会产生荧光信号。即使在间期固定时也能清晰检测到信号,这提高了结果的准确性,因为在某些情况下获取有丝分裂样本极其困难。FISH目前仍主要用于研究,但也有诊断应用。为了定义许多在FISH之前未被区分的畸变,正在制定新的命名法。FISH可迅速检测非整倍体和恶性肿瘤的产前诊断,在危急情况下非常有用。在一些染色体异常过于复杂而难以手动分类的肿瘤中,比较基因组杂交(CGH)技术,即一种竞争性FISH,可让检查人员确定染色体的全部或部分增减情况。CGH结果可对许多肿瘤细胞系进行分类,并且与其他互补技术(如显微切割-FISH、引物原位标记等)一起,增加了为癌症患者选择合适治疗方法的可能性。

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