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乳腺导管原位癌中17号染色体上的等位基因缺失。

Allelic loss on a chromosome 17 in ductal carcinoma in situ of the breast.

作者信息

Radford D M, Fair K, Thompson A M, Ritter J H, Holt M, Steinbrueck T, Wallace M, Wells S A, Donis-Keller H R

机构信息

Division of Human Molecular Genetics, Washington University School of Medicine, St. Louis, Missouri 63110.

出版信息

Cancer Res. 1993 Jul 1;53(13):2947-9.

PMID:8391383
Abstract

Multiple tumor suppressor genes are implicated in the oncogenesis and progression of invasive carcinoma of the breast. To investigate the chronology of genetic changes we studied loss of heterozygosity on chromosome 17 in ductal carcinoma in situ, a preinvasive breast cancer. A microdissection technique was used to separate tumor from normal stromal cells prior to DNA extraction and loss of heterozygosity was assayed mainly using simple sequence repeat polymorphism markers and the polymerase chain reaction. Loss of heterozygosity on 17p was observed in 8 of 28 tumors (29%) when compared with normal control DNA, whereas no loss was seen on 17q, suggesting that at least one locus on 17p is involved early in the development of breast cancer.

摘要

多个肿瘤抑制基因与乳腺浸润性癌的发生和进展有关。为了研究基因改变的时间顺序,我们研究了导管原位癌(一种乳腺浸润前癌)中17号染色体上杂合性缺失的情况。在DNA提取之前,采用显微切割技术将肿瘤细胞与正常基质细胞分离,主要使用简单序列重复多态性标记和聚合酶链反应来检测杂合性缺失。与正常对照DNA相比,28个肿瘤中有8个(29%)观察到17p杂合性缺失,而17q未观察到杂合性缺失,这表明17p上至少有一个位点在乳腺癌发生早期就已受累。

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