Wang Yan, Wang Ziliang, Qi Zihao, Yin Sheng, Zhang Na, Liu Yang, Liu Mingming, Meng Jiao, Zang Rongyu, Zhang Zhen, Yang Gong
Cancer Institute, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Mol Cancer. 2014 Apr 28;13:94. doi: 10.1186/1476-4598-13-94.
It is well known that the activation of Aurora A/B (Aur A/B) or inactivation of BRCA1/2 induces tumor formation. Others and we have reported that the mutual suppression between Aur A/B and BRCA1/2 may manipulate cancer cell growth and tumorigenesis, however, the interactive regulation and mechanism between these molecules are still elusive. In this study, by consecutive silencing of Aur A/B or/and BRCA1/2 with specific shRNAs, we showed that, in BRCA2-deficient pancreatic cancer cell line Capan-1 and in ovarian cancer cell line OVCA433, Aur A/B and BRCA1/2 inversely regulated the expression of each other likely through proteasome-mediated proteolysis but not through gene transcription. Aur A/B and BRCA1/2 conversely regulated cell cycle progression mainly through control of p53 and cyclin A. Moreover, the disruption of Aur A/B blocked abnormal cytokinesis and decreased cell multinuclearity and chromosome tetraploidy, whereas the deprivation of BRCA1/2 promoted the abnormal cytokinesis and enhanced the cell multinuclearity and tetraploidy. Furthermore, we showed by animal assays that the depletion of Aur A/B inhibited tumor growth of both cell lines, while the knockdown of BRCA1/2 promoted the tumor growth. However, the concurrent silencing of Aur A/B and BRCA1/2 diminished the effects of these molecules on the regulation of cell cycle, cytokinesis, and tetraploidy, leading to the burdened tumor sizes similar to those induced by scrambled shRNA-treated control cells. In summary, our study revealed that the negative interplay between Aur A/B and BRCA1/2 inversely controls the cell proliferation, cell cycle progression, cell multinuclearity, and tetraploidization to modulate tumorigenesis.
众所周知,极光激酶A/B(Aur A/B)的激活或乳腺癌1/2基因(BRCA1/2)的失活会诱导肿瘤形成。我们和其他人曾报道,Aur A/B与BRCA1/2之间的相互抑制可能会调控癌细胞的生长和肿瘤发生,然而,这些分子之间的相互调控及其机制仍不清楚。在本研究中,我们通过用特异性短发夹RNA(shRNA)连续沉默Aur A/B或/和BRCA1/2,发现在BRCA2缺陷的胰腺癌细胞系Capan-1和卵巢癌细胞系OVCA433中,Aur A/B和BRCA1/2可能通过蛋白酶体介导的蛋白水解而非基因转录来反向调节彼此的表达。Aur A/B和BRCA1/2主要通过控制p53和细胞周期蛋白A来反向调节细胞周期进程。此外,Aur A/B的缺失会阻断异常的胞质分裂,减少细胞多核性和染色体四倍体,而BRCA1/2的缺失则会促进异常的胞质分裂,增加细胞多核性和四倍体。此外,我们通过动物实验表明,Aur A/B的缺失会抑制这两种细胞系的肿瘤生长,而BRCA1/2的敲低则会促进肿瘤生长。然而,同时沉默Aur A/B和BRCA1/2会减弱这些分子对细胞周期、胞质分裂和四倍体的调控作用,导致肿瘤大小与乱序shRNA处理的对照细胞诱导的肿瘤大小相似。总之,我们的研究表明,Aur A/B与BRCA1/2之间的负向相互作用反向控制细胞增殖、细胞周期进程、细胞多核性和四倍体化,从而调节肿瘤发生。