Yanushko Darya, German Falcon Beatriz, El Bizri Rana, Pervizou Despoina, Dolgos Robin, Keime Céline, Ye Tao, Thibault-Carpentier Christelle, Le Magnen Clementine, Henri Sandrine, Laverny Gilles, Metzger Daniel
Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, France.
Centre National de la Recherche Scientifique (CNRS), Illkirch, France.
Cell Death Dis. 2025 Jan 26;16(1):46. doi: 10.1038/s41419-025-07361-1.
Prostate cancer is a heterogeneous disease with a slow progression and a highly variable clinical outcome. The tumor suppressor genes PTEN and TP53 are frequently mutated in prostate cancer and are predictive of early metastatic dissemination and unfavorable patient outcomes. The progression of solid tumors to metastasis is often associated with increased cell plasticity, but the complex events underlying TP53-loss-induced disease aggressiveness remain incompletely understood. Using genetically engineered mice, we show that Trp53 deficiency in Pten-null prostatic epithelial cells (PECs) does not impact early cell proliferation and neoplasia formation, nor growth arrest and senescence entry at a later time. However, Trp53-deficiency enhances invasive adenocarcinoma development and promotes metastatic cell dissemination. Importantly, our single-cell transcriptomic and chromatin accessibility analyses combined with histological examinations uncovered an epithelial cell population characterized by an induction of Jak/Stat3 signaling and displaying mesenchymal features. Moreover, we show that the transcriptomic signature of this cell population is prominent in tumors of patients with high-risk prostate cancer or metastatic disease. In addition, our in vivo and organoid-based experiments provide evidence that PEC plasticity occurs through bi-directional communication with cancer-associated fibroblasts (CAFs). Thus, our study demonstrates that p53 loss induces a protumorigenic crosstalk between PECs and CAFs, and identifies new vulnerabilities that might be targeted to limit cancer progression.
前列腺癌是一种异质性疾病,进展缓慢,临床结局高度可变。肿瘤抑制基因PTEN和TP53在前列腺癌中经常发生突变,可预测早期转移扩散和患者的不良预后。实体瘤向转移的进展通常与细胞可塑性增加有关,但TP53缺失诱导疾病侵袭性的复杂事件仍未完全了解。利用基因工程小鼠,我们发现Pten基因缺失的前列腺上皮细胞(PEC)中Trp53的缺失不影响早期细胞增殖和肿瘤形成,也不影响后期的生长停滞和衰老进入。然而,Trp53缺失会增强浸润性腺癌的发展并促进转移细胞的扩散。重要的是,我们的单细胞转录组和染色质可及性分析结合组织学检查发现了一个上皮细胞群体,其特征是Jak/Stat3信号的诱导并表现出间充质特征。此外,我们表明,该细胞群体的转录组特征在高危前列腺癌或转移性疾病患者的肿瘤中很突出。此外,我们的体内和基于类器官的实验提供了证据,表明PEC可塑性通过与癌症相关成纤维细胞(CAF)的双向通讯发生。因此,我们的研究表明p53缺失诱导了PEC和CAF之间的促肿瘤串扰,并确定了可能被靶向以限制癌症进展的新弱点。