Giulietti Matteo, Occhipinti Giulia, Righetti Alessandra, Bracci Massimo, Conti Alessandro, Ruzzo Annamaria, Cerigioni Elisabetta, Cacciamani Tiziana, Principato Giovanni, Piva Francesco
Department of Specialistic Clinical and Odontostomatological Sciences, Polytechnic University of Marche, Ancona, Italy.
Department of Clinical and Molecular Sciences, Polytechnic University of Marche, Ancona, Italy.
Front Oncol. 2018 Oct 12;8:450. doi: 10.3389/fonc.2018.00450. eCollection 2018.
Bladder cancer is a very common malignancy. Although new treatment strategies have been developed, the identification of new therapeutic targets and reliable diagnostic/prognostic biomarkers for bladder cancer remains a priority. Generally, they are found among differentially expressed genes between patients and healthy subjects or among patients with different tumor stages. However, the classical approach includes processing these data taking into consideration only the expression of each single gene regardless of the expression of other genes. These complex gene interaction networks can be revealed by a recently developed systems biology approach called Weighted Gene Co-expression Network Analysis (WGCNA). It takes into account the expression of all genes assessed in an experiment in order to reveal the clusters of co-expressed genes (modules) that, very probably, are also co-regulated. If some genes are co-expressed in controls but not in pathological samples, it can be hypothesized that a regulatory mechanism was altered and that it could be the cause or the effect of the disease. Therefore, genes within these modules could play a role in cancer and thus be considered as potential therapeutic targets or diagnostic/prognostic biomarkers. Here, we have reviewed all the studies where WGCNA has been applied to gene expression data from bladder cancer patients. We have shown the importance of this new approach in identifying candidate biomarkers and therapeutic targets. They include both genes and miRNAs and some of them have already been identified in the literature to have a role in bladder cancer initiation, progression, metastasis, and patient survival.
膀胱癌是一种非常常见的恶性肿瘤。尽管已经开发了新的治疗策略,但确定膀胱癌的新治疗靶点和可靠的诊断/预后生物标志物仍然是当务之急。一般来说,它们存在于患者与健康受试者之间或不同肿瘤阶段患者之间差异表达的基因中。然而,传统方法仅考虑每个单一基因的表达来处理这些数据,而不考虑其他基因的表达。最近开发的一种称为加权基因共表达网络分析(WGCNA)的系统生物学方法可以揭示这些复杂的基因相互作用网络。它考虑了实验中评估的所有基因的表达,以揭示共表达基因(模块)的簇,这些簇很可能也受到共同调控。如果某些基因在对照中共同表达而在病理样本中不共同表达,则可以假设一种调节机制发生了改变,并且它可能是疾病的原因或结果。因此,这些模块中的基因可能在癌症中起作用,从而被视为潜在的治疗靶点或诊断/预后生物标志物。在这里,我们回顾了所有将WGCNA应用于膀胱癌患者基因表达数据的研究。我们已经展示了这种新方法在识别候选生物标志物和治疗靶点方面的重要性。它们包括基因和miRNA,其中一些已经在文献中被确定在膀胱癌的发生、进展、转移和患者生存中起作用。