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正常发育和肿瘤发生过程中小鼠乳腺中Brca1及其剪接变体Brca1delta11 RNA水平的表达

Expression of Brca1 and splice variant Brca1delta11 RNA levels in mouse mammary gland during normal development and tumorigenesis.

作者信息

Mixon M, Kittrell F, Medina D

机构信息

Department of Cell Biology, Baylor College of Medicine, One Baylor Plaza, Houston, Texas, TX 77030, USA.

出版信息

Oncogene. 2000 Nov 2;19(46):5237-43. doi: 10.1038/sj.onc.1203905.

Abstract

Expression of Brca1 in mouse mammary cancer has yet to be analysed. We use a progressive model of neoplasia based on several mouse epithelial cell lines that represent distinct steps toward the fully tumorigenic state. Using RNase protection analysis because acceptable anti-Brca1 antibodies are not available we investigated the expression of Brca1 and a splice variant, Brca1Delta11, in several mammary hyperplasias and tumors that arose from them, and in normal mammary gland through pregnancy and involution. Expression of Brca1 was highest in rapidly proliferating cells. Expression of the full-length Brca1 was detectable in the virgin gland, was slightly elevated in the midpregnant gland, and decreased to levels similar to the age-matched virgin gland in the completely involuted gland. Expression of both forms of Brca1 was detectable in 9/9 paired hyperplasias and tumors, with levels of total Brca1, but not the splice variant Brca1Delta11, in tumors higher than those in the hyperplasias. While in disagreement with the observation that Brca1 levels decrease in human breast cancer progression, these patterns support the notion that Brca1 expression is associated with proliferating cells, and suggests that the link with differentiation seen in normal cells can be removed when cells become tumorigenic.

摘要

Brca1在小鼠乳腺癌中的表达尚未得到分析。我们使用了一种基于几种小鼠上皮细胞系的肿瘤形成渐进模型,这些细胞系代表了向完全致瘤状态发展的不同阶段。由于没有可用的可接受的抗Brca1抗体,我们使用核糖核酸酶保护分析方法,研究了Brca1及其剪接变体Brca1Delta11在几种乳腺增生症及其引发的肿瘤以及正常乳腺在怀孕和退化过程中的表达情况。Brca1在快速增殖的细胞中表达最高。全长Brca1在未孕乳腺中可检测到,在怀孕中期乳腺中略有升高,在完全退化的乳腺中降至与年龄匹配的未孕乳腺相似的水平。在9/9对的增生症和肿瘤中均可检测到两种形式的Brca1的表达,肿瘤中总Brca1的水平高于增生症中的水平,但剪接变体Brca1Delta11的水平并非如此。虽然这与人类乳腺癌进展过程中Brca1水平降低的观察结果不一致,但这些模式支持了Brca1表达与增殖细胞相关的观点,并表明当细胞发生肿瘤形成时,与正常细胞中所见的分化的联系可能会被消除。

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