The protein kinase Pak4 disrupts mammary acinar architecture and promotes mammary tumorigenesis.
The protein kinase Pak4 disrupts mammary acinar architecture and promotes mammary tumorigenesis.
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DOI：
10.1038/onc.2010.329
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发表时间：
2010-11-04
期刊：
影响因子：
8
通讯作者：
Minden, A.
中科院分区：
文献类型：
--
作者：
Liu, Y.;Chen, N.;Cui, X.;Zheng, X.;Deng, L.;Price, S.;Karantza, V.;Minden, A.
The Pak4 serine/threonine kinase is highly expressed in many cancer cell lines and human tumors. While several studies have addressed the role for Pak4 in transformation of fibroblasts, most human cancers are epithelial in origin. Epithelial cancers are associated not only with changes in cell growth, but also with changes in the cellular organization within the three dimensional (3D) architecture of the affected tissues. Here we used immortalized mouse mammary epithelial cells (iMMECs) as a model system to study the role for Pak4 in mammary tumorigenesis. iMMECs are an excellent model system for studying breast cancer they can grow in 3D-epithelial cell culture, where they form acinar structures that recapitulate in vivo mammary morphogenesis. While Pak4 is expressed at low levels in wild type iMMECs, it is overexpressed in response to oncogenes, such as oncogenic Ras and Her2/neu. Here we found that overexpression of Pak4 in iMMECs leads to changes in 3D acinar architecture that are consistent with oncogenic transformation. These include decreased central acinar cell death, abrogation of lumen formation, cell polarity alterations, and deregulation of acinar size and cell number. Furthermore, iMMECs overexpressing Pak4 form tumors when implanted into the fat pads of athymic mice. Our results suggest that overexpression of Pak4 triggers events that are important for the transformation of mammary epithelial cells. This is likely to be due to the ability of Pak4 to inhibit apoptosis and promote cell survival, and thus subsequent uncontrolled proliferation, and to its ability to deregulate cell shape and polarity.
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影响因子：
4.8
作者：
Debnath, J;Muthuswamy, SK;Brugge, JS
通讯作者：
Brugge, JS
影响因子：
11.4
作者：
Abo, A;Qu, J;Minden, A
通讯作者：
Minden, A
影响因子：
64.5
作者：
Zhan L;Rosenberg A;Bergami KC;Yu M;Xuan Z;Jaffe AB;Allred C;Muthuswamy SK
通讯作者：
Muthuswamy SK
影响因子：
5.3
作者：
Paliouras, Grigorios N.;Naujokas, Monica A.;Park, Morag
通讯作者：
Park, Morag
影响因子：
56.9
作者：
XIA, ZG;DICKENS, M;GREENBERG, ME
通讯作者：
GREENBERG, ME