Klf5基因缺失通过多种致癌信号通路促进由Pten基因缺失引发的管腔型小鼠前列腺肿瘤。
Klf5 deletion promotes Pten deletion-initiated luminal-type mouse prostate tumors through multiple oncogenic signaling pathways.
作者信息
Xing Changsheng, Ci Xinpei, Sun Xiaodong, Fu Xiaoying, Zhang Zhiqian, Dong Eric N, Hao Zhao-Zhe, Dong Jin-Tang
机构信息
Department of Genetics and Cell Biology, College of Life Sciences, Nankai University, Tianjin, China ; Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA, USA.
Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA, USA.
出版信息
Neoplasia. 2014 Nov 20;16(11):883-99. doi: 10.1016/j.neo.2014.09.006. eCollection 2014 Nov.
Krüppel-like factor 5 (KLF5) regulates multiple biologic processes. Its function in tumorigenesis appears contradictory though, showing both tumor suppressor and tumor promoting activities. In this study, we examined whether and how Klf5 functions in prostatic tumorigenesis using mice with prostate-specific deletion of Klf5 and phosphatase and tensin homolog (Pten), both of which are frequently inactivated in human prostate cancer. Histologic analysis demonstrated that when one Pten allele was deleted, which causes mouse prostatic intraepithelial neoplasia (mPIN), Klf5 deletion accelerated the emergence and progression of mPIN. When both Pten alleles were deleted, which causes prostate cancer, Klf5 deletion promoted tumor growth, increased cell proliferation, and caused more severe morphologic and molecular alterations. Homozygous deletion of Klf5 was more effective than hemizygous deletion. Unexpectedly, while Pten deletion alone expanded basal cell population in a tumor as reported, Klf5 deletion in the Pten-null background clearly reduced basal cell population while expanding luminal cell population. Global gene expression profiling, pathway analysis, and experimental validation indicate that multiple mechanisms could mediate the tumor-promoting effect of Klf5 deletion, including the up-regulation of epidermal growth factor and its downstream signaling molecules AKT and ERK and the inactivation of the p15 cell cycle inhibitor. KLF5 also appears to cooperate with several transcription factors, including CREB1, Sp1, Myc, ER and AR, to regulate gene expression. These findings validate the tumor suppressor function of KLF5. They also yield a mouse model that shares two common genetic alterations with human prostate cancer-mutation/deletion of Pten and deletion of Klf5.
Krüppel样因子5(KLF5)调节多种生物学过程。然而,其在肿瘤发生中的作用似乎相互矛盾,兼具肿瘤抑制和肿瘤促进活性。在本研究中,我们利用前列腺特异性缺失Klf5和磷酸酶及张力蛋白同源物(Pten)的小鼠,研究Klf5在前列腺肿瘤发生中的作用及机制,这两种基因在人类前列腺癌中常发生失活。组织学分析表明,当一个Pten等位基因缺失时,可导致小鼠前列腺上皮内瘤变(mPIN),而Klf5缺失会加速mPIN的出现和进展。当两个Pten等位基因均缺失时,可导致前列腺癌,Klf5缺失会促进肿瘤生长,增加细胞增殖,并引起更严重的形态学和分子改变。Klf5纯合缺失比杂合缺失更有效。出乎意料的是,正如报道的那样,单独缺失Pten会使肿瘤中的基底细胞群体增加,而在Pten缺失背景下缺失Klf5则明显减少基底细胞群体,同时增加管腔细胞群体。全基因组表达谱分析、通路分析和实验验证表明,多种机制可介导Klf5缺失的肿瘤促进作用,包括表皮生长因子及其下游信号分子AKT和ERK的上调以及p15细胞周期抑制剂的失活。KLF5似乎还与几种转录因子协同作用,包括CREB1、Sp1、Myc、ER和AR,以调节基因表达。这些发现证实了KLF5的肿瘤抑制功能。它们还产生了一种与人类前列腺癌具有两种共同基因改变的小鼠模型——Pten的突变/缺失和Klf5的缺失。