Jensen R A, Page D L, Holt J T
Department of Pathology, Vanderbilt University School of Medicine, Nashville, TN 37232.
Proc Natl Acad Sci U S A. 1994 Sep 27;91(20):9257-61. doi: 10.1073/pnas.91.20.9257.
Histopathologic study of human breast biopsy samples has identified specific lesions which are associated with a high risk of development of invasive breast cancer. Presumably, these lesions (collectively termed premalignant breast disease) represent the earliest recognizable morphologic expression of fundamental molecular events that lead to the development of invasive breast cancer. To study molecular events underlying premalignant breast disease, we have developed a method for isolating RNA from histologically identified lesions from frozen human breast tissue. This method specifically obtains mRNA from breast epithelial cells and has identified three genes which are differentially expressed in premalignant breast epithelial lesions. One gene identified by this method is overexpressed in four of five noncomedo ductal carcinoma in situ lesions and appears to be the human homologue of the gene encoding the M2 subunit of ribonucleotide reductase, an enzyme involved in DNA synthesis.
对人类乳腺活检样本的组织病理学研究已确定了一些特定病变,这些病变与浸润性乳腺癌的高发病风险相关。据推测,这些病变(统称为癌前乳腺疾病)代表了导致浸润性乳腺癌发生的基本分子事件最早可识别的形态学表现。为了研究癌前乳腺疾病背后的分子事件,我们开发了一种从冷冻人类乳腺组织的组织学鉴定病变中分离RNA的方法。该方法专门从乳腺上皮细胞中获取mRNA,并已鉴定出三个在癌前乳腺上皮病变中差异表达的基因。通过这种方法鉴定出的一个基因在五分之四的非粉刺性导管原位癌病变中过度表达,并且似乎是编码核糖核苷酸还原酶M2亚基的基因的人类同源物,核糖核苷酸还原酶是一种参与DNA合成的酶。