Gomez Eduardo Wandame, De Paula Laura Berti, Weimer Rafael Diogo, Hellwig Alessandra Helena da Silva, Rodrigues Grazielle Motta, Alegretti Ana Paula, de Oliveira Jarbas Rodrigues
Laboratory of Cell Biophysics and Inflammation, School of Health and Life Sciences, Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre, Brazil.
Laboratory of Molecular Biology, Laboratory Diagnostic Service, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.
Front Oncol. 2024 Mar 5;14:1330592. doi: 10.3389/fonc.2024.1330592. eCollection 2024.
Chronic myeloid leukemia (CML) is a myeloproliferative disorder characterized by leukocytosis and left shift. The primary molecular alteration is the BCR::ABL1, chimeric oncoprotein with tyrosine kinase activity, responsible for the initial oncogenesis of the disease. Therapy of CML was revolutionized with the advent of tyrosine kinase inhibitors, but it is still not considered curative and may present resistance and serious adverse effects. Discoveries in CML inaugurated a new era in cancer treatment and despite all the advances, a new biomarker is needed to detect resistance and adverse effects. Circular RNAs (circRNAs) are a special type of non-coding RNA formed through a process called backsplicing. The majority of circRNAs are derived from protein-coding genes. CircHIPK3 is formed from the second exon of the HIPK3 gene and has been found in various pathologies, including different types of cancer. New approaches have demonstrated the potential of circular RNAs in cancer research, and circHIPK3 has shown promising results. It is often associated with cellular regulatory pathways, suggesting an important role in the molecular dynamics of tumors. The identification of biomarkers is an important tool for therapeutic improvement; thus we review the role of circHIPK3 and its potential as a biomarker in CML.
慢性髓性白血病(CML)是一种以白细胞增多和核左移为特征的骨髓增殖性疾病。主要分子改变是具有酪氨酸激酶活性的BCR::ABL1嵌合癌蛋白,它是该疾病初始肿瘤发生的原因。随着酪氨酸激酶抑制剂的出现,CML的治疗发生了革命性变化,但仍不被认为是治愈性的,并且可能出现耐药性和严重不良反应。CML的研究发现开创了癌症治疗的新纪元,尽管取得了所有这些进展,但仍需要一种新的生物标志物来检测耐药性和不良反应。环状RNA(circRNA)是一种通过称为反向剪接的过程形成的特殊类型的非编码RNA。大多数circRNA来源于蛋白质编码基因。CircHIPK3由HIPK3基因的第二个外显子形成,已在包括不同类型癌症在内的各种病理状态中被发现。新方法已经证明了环状RNA在癌症研究中的潜力,circHIPK3已显示出有前景的结果。它经常与细胞调节途径相关,表明在肿瘤分子动力学中起重要作用。生物标志物的鉴定是改善治疗的重要工具;因此,我们综述了circHIPK3的作用及其作为CML生物标志物的潜力。