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Polo样激酶5在癌症中的潜在肿瘤抑制作用。

Potential Tumor Suppressor Role of Polo-like Kinase 5 in Cancer.

作者信息

Su Shengqin, Ndiaye Mary Ann, Guzmán-Pérez Glorimar, Baus Rebecca Michael, Huang Wei, Patankar Manish Suresh, Ahmad Nihal

机构信息

Department of Dermatology, University of Wisconsin, Madison, WI 53705, USA.

Department of Pathology and Laboratory Medicine, University of Wisconsin, Madison, WI 53705, USA.

出版信息

Cancers (Basel). 2023 Nov 17;15(22):5457. doi: 10.3390/cancers15225457.

Abstract

The polo-like kinase (PLK) family of serine/threonine kinases contains five members (PLK1-5). Most PLKs are involved in cell cycle regulation and DNA damage response. However, PLK5 is different as it lacks a functional kinase domain and is not involved in cell cycle control. PLK5 remains the least-studied family member, and its role in oncogenesis remains enigmatic. Here, we identified tissues with high PLK5 expression by leveraging the Protein Atlas and GTEx databases with relevant literature and selected ovarian, lung, testis, endometrium, cervix, and fallopian tube tissues as candidates for further investigation. Subsequently, we performed immunohistochemical staining for PLK5 on multiple tissue microarrays followed by Vectra scanning and quantitative inForm analysis. This revealed consistently downregulated PLK5 expression in these cancers compared to normal tissues. To validate and extend our findings, we performed pan-cancer analysis of expression using public RNAseq databases (TCGA and GTEx). We found is downregulated in 18 cancer types, including our selected candidates. Interestingly, we also observed PLK5 expression remains consistently low in later stages of cancer, suggesting PLK5 may have a greater role in tumor initiation than cancer progression. Overall, our study demonstrates PLK5 downregulation in multiple cancers, highlighting its role as a tumor suppressor.

摘要

丝氨酸/苏氨酸激酶的polo样激酶(PLK)家族包含五个成员(PLK1 - 5)。大多数PLK参与细胞周期调控和DNA损伤反应。然而,PLK5有所不同,因为它缺乏功能性激酶结构域,不参与细胞周期控制。PLK5仍然是研究最少的家族成员,其在肿瘤发生中的作用仍然成谜。在这里,我们通过利用蛋白质图谱和GTEx数据库以及相关文献,确定了PLK5高表达的组织,并选择卵巢、肺、睾丸、子宫内膜、子宫颈和输卵管组织作为进一步研究的候选对象。随后,我们在多个组织微阵列上对PLK5进行免疫组织化学染色,然后进行Vectra扫描和定量inForm分析。结果显示,与正常组织相比,这些癌症中PLK5的表达持续下调。为了验证和扩展我们的发现,我们使用公共RNAseq数据库(TCGA和GTEx)对表达进行泛癌分析。我们发现PLK5在18种癌症类型中表达下调,包括我们选择的候选对象。有趣的是,我们还观察到PLK5在癌症后期的表达一直很低,这表明PLK5在肿瘤起始阶段可能比癌症进展中发挥更大的作用。总体而言,我们的研究证明了PLK5在多种癌症中的下调,突出了其作为肿瘤抑制因子的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dcc/10669931/391104c8e9b9/cancers-15-05457-g001.jpg

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