乳腺癌中的 Speedy/RINGO 蛋白作为未来生物标志物的作用。

Cancer diagnosis & prognosis Pub Date : 2024-05-03 eCollection Date: 2024-05-01 DOI:10.21873/cdp.10310
Ozgur Tanriverdi, Aysegul Yildiz
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引用次数: 0

摘要

背景/目的:细胞周期蛋白依赖性激酶(CDKs)是一种需要与称为细胞周期蛋白的调控亚基结合的蛋白质,在细胞周期的进展和活化中起着关键作用。CDK 在许多实体恶性肿瘤的致癌过程中发挥着关键作用,临床前研究表明,抑制这些蛋白可产生抗癌效果。本叙述性综述旨在开发一种假设性方法,以确定与 CDK2 相关的蛋白质 Speedy/RINGO 是否可能成为接受 CDK4/6 抑制剂治疗的乳腺癌患者的预测因素:在 PubMed、Web of Science、Medline 和 Google Scholars 搜索引擎上进行文献检索,以匹配以下词条:"Speedy/RINGO "或 "Spy1 "和 "CDKs "或 "依赖细胞周期蛋白的激酶(CDKs)"和 "CDK4/6 抑制剂 "和 "调节 "和 "分子 "和 "乳腺癌 "和 "致癌"。只有在分子水平上研究 Speedy/RINGO 蛋白和 CDK 之间关系的文章才被收录。通过尝试建立与我们的假设问题之间的关系,对文献信息进行了汇编:Speedy/RINGO是一种受到严格调控的哺乳动物原癌蛋白,在体细胞周期中发挥着重要作用。研究强调,虽然它与细胞周期蛋白没有氨基酸序列同源性,但它能激活 CDK2。此外,通过激活 CDK2 对 CDK4/6 抑制作用进行分子补偿的结果也表明,CDK2 可以预测耐药性。另一个重要发现是,在CDK4/6抑制剂治疗期间,过表达的Speedy/RINGO可强烈激活CDK2,从而导致对治疗的负反应:尽管已经研究了许多预测因素,以显示对 CDK4/6 抑制剂的反应或确定耐药性,但尚未建立一个共识生物标志物。根据我们的综述所获得的信息,可以得出结论:Speedy/RINGO 蛋白作为一种预测性生物标志物,可能对 CDK4/6 抑制剂治疗患者的治疗反应、治疗持续性和耐药性具有重要作用。
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The Role of Speedy/RINGO Protein in Breast Cancer as a Future Biomarker.

Background/aim: Cyclin-dependent kinases (CDKs) are proteins that require the binding of regulatory subunits called cyclins and play a key role in cell cycle progression and activation. CDKs play a key role in carcinogenesis of many solid malignancies, and inhibition of these proteins has produced anti-cancer effects demonstrated in preclinical studies. This narrative review was conducted to develop a hypothetical approach to determine whether Speedy/RINGO, a protein associated with CDK2, could be a possible predictive factor in breast cancer patients treated with a CDK4/6 inhibitor.

Materials and methods: A literature search was conducted in PubMed, Web of Science, Medline, and Google Scholars search engines to match the following words: "Speedy/RINGO" or "Spy1" and "CDKs" or "Cyclin-dependent kinases (CDKs)" and "CDK4/6 inhibitors" and "Regulation" and "Molecular" and "Breast cancer" and "Carcinogenesis". Only articles investigating the relationship between the Speedy/RINGO protein and CDKs at the molecular level were included. Literature information was compiled by trying to establish a relationship with our hypothesis question.

Results: Speedy/RINGO is a tightly regulated proto-oncogenic mammalian protein playing important roles in the somatic cell cycle. Studies have emphasized that although it does not have amino acid sequence homology with cyclins, it can activate CDK2. In addition, results showing molecular compensation of CDK4/6 inhibition through CDK2 activation, also showed that CDK2 can predict drug resistance. Another important finding was that overexpressed Speedy/RINGO, during CDK4/6 inhibitor treatment, could strongly activate CDK2, resulting in a negative response to treatment.

Conclusion: Although many predictive factors have been investigated to indicate response to CDK4/6 inhibitors or determine drug resistance, a consensus biomarker has yet to be established. In light of the information obtained from our review, it can be concluded that the Speedy/RINGO protein may have an important role as a predictive biomarker in terms of response to treatment, continuity of treatment and drug resistance in patients treated with CDK4/6 inhibitors.

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