Patel Girijesh Kumar, Chugh Natasha, Tripathi Manisha
Department of Cell Biology and Biochemistry, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.
Cancers (Basel). 2019 Sep 20;11(10):1405. doi: 10.3390/cancers11101405.
Our understanding of neuroendocrine prostate cancer (NEPC) has assumed a new perspective in light of the recent advances in research. Although classical NEPC is rarely seen in the clinic, focal neuroendocrine trans-differentiation of prostate adenocarcinoma occurs in about 30% of advanced prostate cancer (PCa) cases, and represents a therapeutic challenge. Even though our knowledge of the mechanisms that mediate neuroendocrine differentiation (NED) is still evolving, the role of androgen deprivation therapy (ADT) as a key driver of this phenomenon is increasingly becoming evident. In this review, we discuss the molecular, cellular, and therapeutic mediators of NED, and emphasize the role of the tumor microenvironment (TME) in orchestrating the phenotype. Understanding the role of the TME in mediating NED could provide us with valuable insights into the plasticity associated with the phenotype, and reveal potential therapeutic targets against this aggressive form of PCa.
鉴于最近的研究进展,我们对神经内分泌前列腺癌(NEPC)的理解有了新的视角。虽然经典的NEPC在临床上很少见,但前列腺腺癌的局灶性神经内分泌转分化在约30%的晚期前列腺癌(PCa)病例中出现,这是一个治疗挑战。尽管我们对介导神经内分泌分化(NED)的机制的了解仍在不断发展,但雄激素剥夺疗法(ADT)作为这一现象的关键驱动因素的作用越来越明显。在这篇综述中,我们讨论了NED的分子、细胞和治疗介质,并强调了肿瘤微环境(TME)在协调表型方面的作用。了解TME在介导NED中的作用可以为我们提供有关该表型可塑性的宝贵见解,并揭示针对这种侵袭性PCa形式的潜在治疗靶点。