Rosalind and Morris Goodman Cancer Research Centre, McGill University, 1160 Pine Avenue West, Montréal, QC H3A 1A3, Canada.
Institut de Génétique, Reproduction et Développement, Université Clermont Auvergne, CNRS UMR6293, INSERM U1103, 28 Place Henri Dunant, BP38, 63001 Clermont-Ferrand, France.
Cells. 2021 Sep 10;10(9):2387. doi: 10.3390/cells10092387.
Prostate cancer is the most common cancer in aging men. Despite recent progress, there are still few effective treatments to cure its aggressive and metastatic stages. A better understanding of the molecular mechanisms driving disease initiation and progression appears essential to support the development of more efficient therapies and improve patient care. To do so, multiple research models, such as cell culture and mouse models, have been developed over the years and have improved our comprehension of the biology of the disease. Recently, a new model has been added with the use of the accessory gland. With a high level of conservation of major signaling pathways implicated in human disease, this functional equivalent of the prostate represents a powerful, inexpensive, and rapid in vivo model to study epithelial carcinogenesis. The purpose of this review is to quickly overview the existing prostate cancer models, including their strengths and limitations. In particular, we discuss how the accessory gland can be integrated as a convenient complementary model by bringing new understanding in the mechanisms driving prostate epithelial tumorigenesis, from initiation to metastatic formation.
前列腺癌是老年男性中最常见的癌症。尽管最近取得了一些进展,但对于侵袭性和转移性阶段的治疗方法仍然很少。更好地了解驱动疾病发生和进展的分子机制对于支持更有效的治疗方法的开发和改善患者护理至关重要。为此,多年来已经开发了多种研究模型,如细胞培养和小鼠模型,这些模型提高了我们对疾病生物学的理解。最近,随着附属腺的使用,增加了一种新的模型。由于涉及人类疾病的主要信号通路具有高度保守性,这种前列腺的功能等效物代表了一种强大、廉价且快速的体内模型,可用于研究上皮癌发生。本文的目的是快速概述现有的前列腺癌模型,包括它们的优点和局限性。特别是,我们讨论了如何通过将附属腺整合为一种方便的互补模型,从起始到转移形成,在驱动前列腺上皮肿瘤发生的机制方面带来新的认识。