Department of Laboratory Medicine, The Affiliated Hospital of Southwest Medical University, Sichuan, China.
J Cell Mol Med. 2021 Aug;25(15):7307-7320. doi: 10.1111/jcmm.16760. Epub 2021 Jun 30.
Breast cancer (BC) is a molecular diverse disease which becomes the most common malignancy among women worldwide. There are four BC subtypes (Luminal A, Luminal B, HER2-enriched and Basal-like) robustly established following gene expression pattern-based characterization, behave significant differences in terms of their incidence, risk factors, prognosis and therapeutic sensitivity. Thus, there is an urgent need to provide mechanism research, treatment strategies and/or prognosis evaluation based on the patient stratification of BC subtypes. The prostate-derived ETS factor SPDEF was first identified as an activator of prostate specific antigen, and then, the involvements in many aspects of BC have been proposed. However, the subtype-specific molecular function of SPDEF in BC and insights into prognostic significance have not been clearly elucidated. This study demonstrated for the first time that SPDEF may play a diversity role in the expression levels, clinicopathologic importance, biological function and prognostic evaluation in BC via bioinformatics and experimental evidence, which mainly depends on different BC subtyping. In summary, our findings would help to better understand the possible mechanisms of various BC subtypes and to find possible candidate genes for prognostic and therapeutic usage.
乳腺癌(BC)是一种分子多样性疾病,已成为全球女性中最常见的恶性肿瘤。根据基于基因表达模式的特征,现已确立了四种 BC 亚型(Luminal A、Luminal B、HER2 富集型和基底样),它们在发病、风险因素、预后和治疗敏感性方面存在显著差异。因此,迫切需要根据 BC 亚型的患者分层提供机制研究、治疗策略和/或预后评估。前列腺衍生的 ETS 因子 SPDEF 最初被鉴定为前列腺特异性抗原的激活剂,随后提出了其在 BC 许多方面的参与。然而,SPDEF 在 BC 中的亚型特异性分子功能以及对预后意义的了解尚不清楚。本研究首次通过生物信息学和实验证据表明,SPDEF 可能通过不同的 BC 亚分型在 BC 中的表达水平、临床病理重要性、生物学功能和预后评估中发挥多样性作用。总之,我们的研究结果将有助于更好地理解各种 BC 亚型的可能机制,并找到可能用于预后和治疗的候选基因。