CircularRNA abhydrolase domain containing 16A-microRNA-1237-5p-apoptosis associated tyrosine kinase axis regulates the apoptosis of michigan cancer foundation-7 in breast cancer cells

Z-G Sheng, Zhuanji Jiang, Binming Zhang
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Abstract

Objective To investigate the circular RNA abhydrolase domain containing 16A (circRNA ABHD16A)-microRNA (miRNA, miR)-1237-5p-Apoptosis associated tyrosine kinase (AATK) axis on apoptosis of breast cancer cell munggan cancer foundation-7 (MCF-7). Methods The correlation between ABHD16A and miR-1237-5p and miR-1237-5p and AATK was analyzed by CSCD and TargetScan online analysis. The luciferase assay was used to detect whether circRNA ABHD16A targets miR-1237-5p and whether miR-1237-5p targets AATK. The expression of apoptotic marker proteins in AATK and breast cancer cells MCF-7 was detected by Western blot after over-expression or knockdown of circRNA ABHD16A. Cell viability of breast cancer cells MCF-7 was analyzed by methyl thiazolyl tetrazolium (MTT) assay; staining by Annexin-V was performed by MTT assay. The level of apoptosis of breast cancer cells MCF-7 was measured. Student’s t-test analyzed two sets of one-way analysis of variance. Results circRNA ABHD16A targets miR-1237-5p; miR-1237-5p targets the 320-326 and 469-475 regions of the AATK 3’ UTR. When overexpressing ABHD16A, AATK expression increased significantly (t=15.295, P<0.01), apoptosis-related protein bcl-2 antagonist/killer 1 (bak), bcl-2 Associated X Apoptosis Regulator (bax) and cleaved Caspase-9 (cleaved-CAS9) expression levels increased significantly (t=7.403, 8.381, 21.583, P<0.01). The expression of bcl-2 Apoptosis Regulator (bcl-2) was significantly decreased (t=6.301, P<0.01), the activity of MCF7 cells was decreased (t=17.392, P<0.01), and the level of apoptosis was increased (t=8.491, P<0.05). When ABHD16A was knocked down, the expression of AATK was significantly decreased (t=9.290, P<0.01), and the expression levels of apoptosis-related proteins bak, bax and cleaved-CAS9 were significantly decreased (t=8.381, 5.296, 11.492, P<0.01), while the expression of bcl-2 increased significantly (t=5.609, P<0.01), the activity level of MCF7 cells increased (t=5.694, P<0.01), and the level of apoptosis decreased (t=13.502, P<0.01). Conclusion circRNA ABHD16A targets miR-1237-5p and increases the expression of AATK and promotes the apoptosis of breast cancer cells MCF-7. Key words: CircularRNA abhydrolase domain containing 16A; MicroRNA-1237-5p; Apoptosis associated tyrosine kinase; Breast cancer; Michigan cancer foundation-7; Cell apoptosis
含有16a - microrna -1237-5p-凋亡相关酪氨酸激酶轴的CircularRNA abhydrolase结构域调控乳腺癌细胞密歇根癌基础-7的凋亡
目的研究环RNA脱羧酶结构域16A(circRNAABHD16A)-微小RNA(miRNA,miR)-123-75p-凋亡相关酪氨酸激酶(AATK)轴对乳腺癌症细胞癌症基金会7(MCF-7)凋亡的影响。方法采用CSCD和TargetScan在线分析方法,分析ABHD16A与miR-1237-5p、miR-1237-5 p与AATK的相关性。荧光素酶测定用于检测circRNA ABHD16A是否靶向miR-1237-5p以及miR-1237-5-p是否靶向AATK。在过量表达或敲低circRNA ABHD16A后,通过蛋白质印迹检测AATK和乳腺癌症细胞MCF-7中凋亡标记蛋白的表达。采用甲基噻唑四唑(MTT)法检测癌症细胞MCF-7的细胞活力;采用MTT法进行Annexin-V染色。测定癌症细胞MCF-7的凋亡水平。Student的t检验分析了两组单向方差分析。结果circRNA ABHD16A靶向miR-1237-5p;miR-1237-5p靶向AATK 3’UTR的320-326和469-475区域。当过表达ABHD16A时,AATK表达显著增加(t=15.295,P<0.01),凋亡相关蛋白bcl-2拮抗剂/杀伤因子1(bak),bcl-2相关X细胞凋亡调节因子(bax)和裂解型半胱氨酸蛋白酶-9(cleaved-CAS9)的表达水平显著升高(t=7.403,8.381,21.583,P<0.01),bcl-2细胞凋亡调节蛋白(bcl-2)的表达显著降低(t=6.301,P<0.01)、MCF7细胞活性降低(t=17.392,P<0.01),ABHD16A敲低后,AATK的表达显著降低(t=9.290,P<0.01),凋亡相关蛋白bak、bax和裂解型CAS9的表达显著下降(t=8.381,5.296,11.492,P<0.01);bcl-2的表达显著增加(t=5.609,P<0.01),结论circRNAABHD16A靶向miR-1237-5p,增加AATK的表达,促进癌症MCF-7细胞凋亡。关键词:CircularRNA反水解酶结构域含16A;MicroRNA-1237-5p;细胞凋亡相关酪氨酸激酶;癌症;密歇根癌症基金会-7;细胞凋亡
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