Laboratory of Chromatin Biology and Epigenetics, The Rockefeller University, New York, NY 10065.
Bioinformatics Resource Center, The Rockefeller University, New York, NY 10065.
Proc Natl Acad Sci U S A. 2020 Oct 13;117(41):25732-25741. doi: 10.1073/pnas.2008017117. Epub 2020 Sep 28.
Bladder cancer prognosis is closely linked to the underlying differentiation state of the tumor, ranging from the less aggressive and most-differentiated luminal tumors to the more aggressive and least-differentiated basal tumors. Sequencing of bladder cancer has revealed that loss-of-function mutations in chromatin regulators and mutations that activate receptor tyrosine kinase (RTK) signaling frequently occur in bladder cancer. However, little is known as to whether and how these two types of mutations functionally interact or cooperate to regulate tumor growth and differentiation state. Here, we focus on loss of the histone demethylase UTX (also known as KDM6A) and activation of the RTK FGFR3, two events that commonly cooccur in muscle invasive bladder tumors. We show that UTX loss and FGFR3 activation cooperate to disrupt the balance of luminal and basal gene expression in bladder cells. UTX localized to enhancers surrounding many genes that are important for luminal cell fate, and supported the transcription of these genes in a catalytic-independent manner. In contrast to UTX, FGFR3 activation was associated with lower expression of luminal genes in tumors and FGFR inhibition increased transcription of these same genes in cell culture models. This suggests an antagonistic relationship between UTX and FGFR3. In support of this model, UTX loss-of-function potentiated FGFR3-dependent transcriptional effects and the presence of UTX blocked an FGFR3-mediated increase in the colony formation of bladder cells. Taken together, our study reveals how mutations in UTX and FGFR3 converge to disrupt bladder differentiation programs that could serve as a therapeutic target.
膀胱癌的预后与肿瘤的基础分化状态密切相关,从侵袭性较低且分化程度较高的腔面肿瘤到侵袭性较强且分化程度较低的基底肿瘤不等。对膀胱癌的测序表明,染色质调节因子的功能丧失突变和激活受体酪氨酸激酶(RTK)信号的突变经常发生在膀胱癌中。然而,目前尚不清楚这两种突变是否以及如何在功能上相互作用或合作,以调节肿瘤生长和分化状态。在这里,我们重点关注组蛋白去甲基酶 UTX(也称为 KDM6A)的缺失和 RTK FGFR3 的激活,这两种事件在肌肉浸润性膀胱癌中经常同时发生。我们表明,UTX 的缺失和 FGFR3 的激活共同破坏了膀胱细胞中腔面和基底基因表达的平衡。UTX 定位于围绕许多对腔面细胞命运很重要的基因的增强子上,并以非催化依赖的方式支持这些基因的转录。与 UTX 相反,FGFR3 的激活与肿瘤中腔面基因的表达降低有关,而 FGFR 抑制则增加了这些相同基因在细胞培养模型中的转录。这表明 UTX 和 FGFR3 之间存在拮抗关系。为了支持这一模型,UTX 功能丧失突变增强了 FGFR3 依赖性转录效应,而 UTX 的存在阻止了 FGFR3 介导的膀胱细胞集落形成的增加。总之,我们的研究揭示了 UTX 和 FGFR3 中的突变如何共同破坏膀胱分化程序,这可能成为治疗靶点。