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Skp2是乳腺癌中一个很有前景的治疗靶点。

Skp2 is a promising therapeutic target in breast cancer.

作者信息

Wang Zhiwei, Fukushima Hidefumi, Inuzuka Hiroyuki, Wan Lixin, Liu Pengda, Gao Daming, Sarkar Fazlul H, Wei Wenyi

机构信息

Department of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.

出版信息

Front Oncol. 2012 Jan 4;1(57). doi: 10.3389/fonc.2011.00057.

Abstract

Breast cancer is the most common type of cancer among American women, and remains the second leading cause of cancer-related death for female in the United States. It has been known that several signaling pathways and various factors play critical roles in the development and progression of breast cancer, such as estrogen receptor, Notch, PTEN, human epidermal growth factor receptor 2, PI3K/Akt, BRCA1, and BRCA2. Emerging evidence has shown that the F-box protein S-phase kinase associated protein 2 (Skp2) also plays an important role in the pathogenesis of breast cancer. Therefore, in this brief review, we summarize the novel functions of Skp2 in the pathogenesis of breast cancer. Moreover, we provide further evidence regarding the state of our knowledge toward the development of novel Skp2 inhibitors especially natural "chemopreventive agents" as targeted approach for the prevention and/or treatment of breast cancer.

摘要

乳腺癌是美国女性中最常见的癌症类型,并且仍然是美国女性癌症相关死亡的第二大主要原因。众所周知,几种信号通路和各种因素在乳腺癌的发生和发展中起着关键作用,如雌激素受体、Notch、PTEN、人表皮生长因子受体2、PI3K/Akt、BRCA1和BRCA2。新出现的证据表明,F-box蛋白S期激酶相关蛋白2(Skp2)在乳腺癌的发病机制中也起着重要作用。因此,在这篇简短的综述中,我们总结了Skp2在乳腺癌发病机制中的新功能。此外,我们提供了更多证据,说明我们对新型Skp2抑制剂尤其是天然“化学预防剂”作为预防和/或治疗乳腺癌的靶向方法的了解情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e70/3355927/bcc0649e1d4f/fonc-01-00057-g001.jpg

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