Department of Neuroscience, UT Southwestern Medical Center, Dallas, Texas.
Quantitative Biomedical Research Center, Peter O'Donnell Jr. School of Public Health, UT Southwestern Medical Center, Dallas, Texas.
Cancer Res. 2024 Nov 4;84(21):3522-3537. doi: 10.1158/0008-5472.CAN-24-1388.
Most patients with prostate adenocarcinoma develop resistance to therapies targeting the androgen receptor (AR). Consequently, a portion of these patients develop AR-independent neuroendocrine (NE) prostate cancer (NEPC), a rapidly progressing cancer with limited therapies and poor survival outcomes. Current research to understand the progression to NEPC suggests a model of lineage plasticity whereby AR-dependent luminal-like tumors progress toward an AR-independent NEPC state. Genetic analysis of human NEPC identified frequent loss of RB1 and TP53, and the loss of both genes in experimental models mediates the transition to a NE lineage. Transcriptomics studies have shown that lineage transcription factors ASCL1 and NEUROD1 are present in NEPC. In this study, we modeled the progression of prostate adenocarcinoma to NEPC by establishing prostate organoids and subsequently generating subcutaneous allograft tumors from genetically engineered mouse models harboring Cre-induced loss of Rb1 and Trp53 with Myc overexpression (RPM). These tumors were heterogeneous and displayed adenocarcinoma, squamous, and NE features. ASCL1 and NEUROD1 were expressed within NE-defined regions, with ASCL1 being predominant. Genetic loss of Ascl1 in this model did not decrease tumor incidence, growth, or metastasis; however, there was a notable decrease in NE identity and an increase in basal-like identity. This study provides an in vivo model to study progression to NEPC and establishes the requirement for ASCL1 in driving NE differentiation in prostate cancer. Significance: Modeling lineage transitions in prostate cancer and testing dependencies of lineage transcription factors have therapeutic implications, given the emergence of treatment-resistant, aggressive forms of neuroendocrine prostate cancer. See related commentary by McQuillen and Brady, p. 3499.
大多数前列腺腺癌患者对靶向雄激素受体 (AR) 的治疗产生耐药性。因此,这些患者中的一部分会发展为 AR 非依赖性神经内分泌 (NE) 前列腺癌 (NEPC),这是一种进展迅速的癌症,治疗方法有限,生存预后较差。目前,为了了解向 NEPC 进展的机制,研究提出了谱系可塑性模型,即 AR 依赖性腔型肿瘤向 AR 非依赖性 NEPC 状态进展。对人 NEPC 的遗传分析表明,RB1 和 TP53 经常缺失,在实验模型中缺失这两个基因可介导向 NE 谱系的转变。转录组学研究表明,谱系转录因子 ASCL1 和 NEUROD1 存在于 NEPC 中。在这项研究中,我们通过建立前列腺类器官,并随后从携带 Cre 诱导的 Rb1 和 Trp53 缺失以及 Myc 过表达的基因工程小鼠模型中生成皮下同种异体移植肿瘤,来模拟前列腺腺癌向 NEPC 的进展 (RPM)。这些肿瘤具有异质性,显示出腺癌、鳞状和 NE 特征。ASCL1 和 NEUROD1 在 NE 定义的区域内表达,其中 ASCL1 占主导地位。在该模型中遗传缺失 Ascl1 不会降低肿瘤的发生率、生长或转移;然而,NE 特征明显减少,基底样特征增加。这项研究提供了一个体内模型来研究向 NEPC 的进展,并确定了 ASCL1 在驱动前列腺癌中 NE 分化中的作用。意义:对前列腺癌中谱系转变进行建模,并测试谱系转录因子的依赖性,鉴于治疗抵抗性、侵袭性神经内分泌前列腺癌的出现,这具有治疗意义。另见 McQuillen 和 Brady 的相关评论,第 3499 页。