P190-B, a Rho-GTPase-activating protein, is differentially expressed in terminal end buds and breast cancer.

G Chakravarty, D Roy, M Gonzales, J Gay, A Contreras, J M Rosen
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Abstract

Microdissection and differential display PCR were used to identify genes preferentially expressed in the highly proliferative terminal end buds (TEBs) in the mammary gland of 45-day-old virgin rats. One clone exhibited 87% homology to the human p190-B gene encoding a novel Rho-Gap. Using in situ hybridization, p190-B was detected in both the TEBs and the terminal ducts, with the highest expression observed in the outer layer of TEBs. During normal mammary gland development, p190-B mRNA expression was highest in the virgin mammary gland and decreased during late pregnancy and lactation. Interestingly, increased levels of p190-B mRNA relative to the normal mammary gland were seen in a subset of murine mammary tumors that appeared to be less well differentiated and potentially more aggressive. Transient transfection of a p190-B expression construct into MCF-10A human mammary epithelial cells resulted in disruption of the actin cytoskeleton, which suggests a role for p190-B in regulating the signaling pathways that influence cell migration and invasion. These results suggest that p190-B may be required for virgin mammary gland development, and its aberrant expression may occur in breast cancer.

P190-B是一种rho - gtpase激活蛋白,在终末芽和乳腺癌中存在差异表达。
采用显微解剖和差异显示PCR技术,对45日龄初生大鼠乳腺高增殖终末芽(TEBs)中优先表达的基因进行鉴定。其中一个克隆与人类编码新型Rho-Gap的p190-B基因具有87%的同源性。原位杂交发现,p190-B在teb和末端导管中均有表达,在teb的外层表达量最高。在正常乳腺发育过程中,p190-B mRNA在初生乳腺中表达最高,在妊娠晚期和哺乳期表达降低。有趣的是,与正常乳腺相比,p190-B mRNA水平升高出现在小鼠乳腺肿瘤的一个亚群中,这些肿瘤分化程度较低,可能更具侵袭性。将p190-B表达构建体短暂转染到MCF-10A人乳腺上皮细胞中,可导致肌动蛋白细胞骨架的破坏,这表明p190-B在调节影响细胞迁移和侵袭的信号通路中发挥作用。这些结果表明,p190-B可能是乳腺发育所必需的,其异常表达可能发生在乳腺癌中。
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