Ghani Muhammad Usman, Shi Junbo, Du Yi, Zhong Liping, Cui Hongjuan
Medical Research Institute, Southwest University, Chongqing 400715, China; State Key Laboratory of Resource Insects, Southwest University, Chongqing 400715, China.
State Key Laboratory of Targeting Oncology, Guangxi Medical University, Nanning, Guangxi 530021, China.
Int J Biol Macromol. 2024 Sep 19;280(Pt 3):135814. doi: 10.1016/j.ijbiomac.2024.135814.
Protein kinase 2 (CK2) is an enzyme ubiquitously present and exhibits extensive kinase activity. It has been strongly linked to tumor progression through the abnormal phosphorylation of key proteins. Research has consistently demonstrated that CK2 is deregulated in various cancer types, with enhanced protein expression and nuclear distribution in tumor cells. CK2 plays a crucial role in a complex network that promotes cell infiltration, migration, proliferation, apoptosis, and cancer progression through multiple pathways, including PI3K/AKT, JAK2/STAT3, ATF4/CDKN1, and HSP90/Cdc37. In addition to its role in cancer growth, there is mounting evidence that CK2 may also affect the immunological dynamics of cancer by altering immune cell functions within the tumor microenvironment, thus facilitating tumor immune evasion. Recent research has increasingly focused on CK2, recognizing it as a therapeutic objective for oncological interventions. This review will critically examine the structure and signaling pathways of CK2, highlighting the significance of further research aimed at enhancing our understanding of the CK2 machinery. Finally, we conclude by refining therapeutic options, notably transitioning from non-pharmacological techniques to strategic CK2 inhibitor use. This development shortens the path to the desired outcome, establishing a pioneering standard in cancer therapy.
蛋白激酶2(CK2)是一种普遍存在的酶,具有广泛的激酶活性。它通过关键蛋白的异常磷酸化与肿瘤进展密切相关。研究一直表明,CK2在各种癌症类型中失调,在肿瘤细胞中蛋白表达增强且呈核分布。CK2在一个复杂的网络中发挥关键作用,该网络通过多种途径促进细胞浸润、迁移、增殖、凋亡和癌症进展,包括PI3K/AKT、JAK2/STAT3、ATF4/CDKN1和HSP90/Cdc37。除了在癌症生长中的作用外,越来越多的证据表明,CK2还可能通过改变肿瘤微环境中的免疫细胞功能来影响癌症的免疫动力学,从而促进肿瘤免疫逃逸。最近的研究越来越关注CK2,将其视为肿瘤干预的治疗靶点。本综述将批判性地审视CK2的结构和信号通路,强调进一步研究以增强我们对CK2机制理解的重要性。最后,我们通过完善治疗选择得出结论,特别是从非药物技术转向战略性使用CK2抑制剂。这一进展缩短了通往预期结果的路径,在癌症治疗中建立了一个开创性的标准。