Shen Jiying, Ma Zhirong, Yang Jin, Qu Tianzhen, Xia Yu, Xu Yingjie, Zhou Ming, Liu Weiwei
Department of General Surgery, Shanghai Tongren Hospital, Shanghai Jiao Tong University School of Medicine, 1111 Xianxia Road, 200336, Shanghai, China.
BMC Cancer. 2024 Apr 23;24(1):511. doi: 10.1186/s12885-024-12199-5.
Although papillary thyroid carcinoma (PTC) has a favorable prognosis, it could affect patient life quality and become a serious threat because of invasion and metastasis. Many investigations have suggested that circular RNAs (circRNAs) are involved in different cancer regulations. Nevertheless, circRNAs role in invasive PTC remains unclear.
In the present investigation, next-generation sequencing was applied to explore abnormal circRNA expression. The expression of circRNA phosphoglycerate dehydrogenase (circPHGDH) in PTC cell lines and tissues were examined. Then, we investigated regulatory mechanism and circPHGDH downstream targets using bioinformatics analysis and luciferase reporting analysis. Then transwell migration, Cell Counting Kit-8 (CCK8) and 5-ethynyl-2'-deoxyuridine (EdU) assays were used for cells migration and proliferation analysis. In vivo metastasis and tumorigenesis assays were also employed to evaluate the circPHGDH role in PTC.
The data showcased that circPHGDH expression increased in both PTC cell lines and tissues, which suggested that circPHGDH functions in PTC progression. circPHGDH downregulation suppressed PTC invasion and proliferation in both in vivo and in vitro experiments. Bioinformatics and luciferase reporter results confirmed that both microRNA (miR)-122-5p and pyruvate kinase M2 subtype (PKM2) were downstream targets of circPHGDH. PKM2 overexpression or miR-122-5p suppression reversed PTC cell invasion and proliferation post silencing circPHGDH by restoring aerobic glycolysis.
Taken together, our research found that circPHGDH downregulation reduced PTC progression via miR-122-5p/PKM2 axis regulation mediated by aerobic glycolysis.
尽管甲状腺乳头状癌(PTC)预后良好,但由于侵袭和转移,它可能影响患者生活质量并构成严重威胁。许多研究表明,环状RNA(circRNA)参与不同的癌症调控。然而,circRNA在侵袭性PTC中的作用仍不清楚。
在本研究中,应用二代测序来探索异常的circRNA表达。检测了circRNA磷酸甘油酸脱氢酶(circPHGDH)在PTC细胞系和组织中的表达。然后,我们使用生物信息学分析和荧光素酶报告分析来研究调控机制和circPHGDH的下游靶点。然后使用Transwell迁移实验、细胞计数试剂盒-8(CCK8)和5-乙炔基-2'-脱氧尿苷(EdU)实验进行细胞迁移和增殖分析。还采用体内转移和肿瘤发生实验来评估circPHGDH在PTC中的作用。
数据显示,circPHGDH在PTC细胞系和组织中的表达均增加,这表明circPHGDH在PTC进展中发挥作用。在体内和体外实验中,circPHGDH下调均抑制了PTC的侵袭和增殖。生物信息学和荧光素酶报告结果证实,微小RNA(miR)-122-5p和丙酮酸激酶M2亚型(PKM2)均为circPHGDH的下游靶点。PKM2过表达或miR-122-5p抑制通过恢复有氧糖酵解逆转了circPHGDH沉默后PTC细胞的侵袭和增殖。
综上所述,我们的研究发现,circPHGDH下调通过有氧糖酵解介导的miR-122-5p/PKM2轴调控降低了PTC进展。