Gao Shujun, Fang Lekun, Phan Liem Minh, Qdaisat Aiham, Yeung Sai-Ching J, Lee Mong-Hong
Obstetrics and Gynecology Hospital Fudan University, Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases, Shanghai 200011, China.
Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA.
Oncotarget. 2015 Sep 29;6(29):28026-41. doi: 10.18632/oncotarget.4731.
Cervical cancer is one of the leading causes of cancer death in women. Human papillomaviruses (HPVs) are the major cause in almost 99.7% of cervical cancer. E6 oncoprotein of HPV and E6-associated protein (E6AP) are critical in causing p53 degradation and malignancy. Understanding the E6AP regulation is critical to develop treating strategy for cervical cancer patients. The COP9 signalosome subunit 6 (CSN6) is involved in ubiquitin-mediated protein degradation. We found that both CSN6 and E6AP are overexpressed in cervical cancer. We characterized that CSN6 associated with E6AP and stabilized E6AP expression by reducing E6AP poly-ubiquitination, thereby regulating p53 activity in cell proliferation and apoptosis. Mechanistic studies revealed that CSN6-E6AP axis can be regulated by EGF/Akt signaling. Furthermore, inhibition of CSN6-E6AP axis hinders cervical cancer growth in mice. Taken together, our results indicate that CSN6 is a positive regulator of E6AP and is important for cervical cancer development.
宫颈癌是女性癌症死亡的主要原因之一。人乳头瘤病毒(HPV)是几乎99.7%的宫颈癌的主要病因。HPV的E6癌蛋白和E6相关蛋白(E6AP)在导致p53降解和恶性肿瘤方面至关重要。了解E6AP的调控对于制定宫颈癌患者的治疗策略至关重要。COP9信号体亚基6(CSN6)参与泛素介导的蛋白质降解。我们发现CSN6和E6AP在宫颈癌中均过度表达。我们鉴定出CSN6与E6AP相关,并通过减少E6AP多聚泛素化来稳定E6AP的表达,从而在细胞增殖和凋亡中调节p53活性。机制研究表明,CSN6-E6AP轴可受表皮生长因子/蛋白激酶B(EGF/Akt)信号传导调节。此外,抑制CSN6-E6AP轴可阻碍小鼠宫颈癌的生长。综上所述,我们的结果表明CSN6是E6AP的正调控因子,对宫颈癌的发展很重要。