Mutuku Shadrack M, Spotbeen Xander, Trim Paul J, Snel Marten F, Butler Lisa M, Swinnen Johannes V
Adelaide Medical School, University of Adelaide, Adelaide, SA 5005, Australia.
South Australian Health and Medical Research Institute (SAHMRI), Adelaide, SA 5000, Australia.
Cancers (Basel). 2022 Mar 27;14(7):1702. doi: 10.3390/cancers14071702.
Due to advances in the detection and management of prostate cancer over the past 20 years, most cases of localised disease are now potentially curable by surgery or radiotherapy, or amenable to active surveillance without treatment. However, this has given rise to a new dilemma for disease management; the inability to distinguish indolent from lethal, aggressive forms of prostate cancer, leading to substantial overtreatment of some patients and delayed intervention for others. Driving this uncertainty is the critical deficit of novel targets for systemic therapy and of validated biomarkers that can inform treatment decision-making and to select and monitor therapy. In part, this lack of progress reflects the inherent challenge of undertaking target and biomarker discovery in clinical prostate tumours, which are cellularly heterogeneous and multifocal, necessitating the use of spatial analytical approaches. In this review, the principles of mass spectrometry-based lipid imaging and complementary gene-based spatial omics technologies, their application to prostate cancer and recent advancements in these technologies are considered. We put in perspective studies that describe spatially-resolved lipid maps and metabolic genes that are associated with prostate tumours compared to benign tissue and increased risk of disease progression, with the aim of evaluating the future implementation of spatial lipidomics and complementary transcriptomics for prognostication, target identification and treatment decision-making for prostate cancer.
由于过去20年里前列腺癌检测和管理方面的进展,现在大多数局限性疾病病例通过手术或放疗有潜在治愈的可能,或者适合进行不治疗的主动监测。然而,这给疾病管理带来了一个新的困境;无法区分惰性与致命、侵袭性前列腺癌形式,导致一些患者过度治疗,而另一些患者干预延迟。导致这种不确定性的是系统治疗新靶点以及可指导治疗决策、选择和监测治疗的经过验证的生物标志物的严重不足。这种进展不足部分反映了在临床前列腺肿瘤中进行靶点和生物标志物发现的固有挑战,临床前列腺肿瘤细胞异质性且多灶性,需要使用空间分析方法。在本综述中,我们考虑了基于质谱的脂质成像和基于互补基因的空间组学技术的原理、它们在前列腺癌中的应用以及这些技术的最新进展。我们对描述与前列腺肿瘤相关的空间分辨脂质图谱和代谢基因的研究进行了展望,这些研究是与良性组织相比以及疾病进展风险增加相关的,目的是评估空间脂质组学和互补转录组学在前列腺癌预后、靶点识别和治疗决策中的未来应用。