A novel peptide encoded by N6-methyladenosine modified circMAP3K4 prevents apoptosis in hepatocellular carcinoma

被引:110
|
作者
Duan, Jin-Ling [1 ,2 ]
Chen, Wei [3 ]
Xie, Juan-Juan [1 ]
Zhang, Mao-Lei [4 ]
Nie, Run-Cong [1 ,5 ]
Liang, Hu [1 ,6 ]
Mei, Jie [1 ,5 ]
Han, Kai [1 ,5 ]
Xiang, Zhi-Cheng [1 ,2 ]
Wang, Feng-Wei [1 ]
Teng, Kai [7 ,8 ]
Chen, Ri-Xin [9 ]
Deng, Min-Hua [1 ,5 ]
Yin, Yi-Xin [1 ]
Zhang, Nu [4 ]
Xie, Dan [1 ,2 ]
Cai, Mu-Yan [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Canc Ctr, Collaborat Innovat Ctr Canc Med, State Key Lab Oncol South China, Guangzhou 510060, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Canc Ctr, Dept Pathol, Guangzhou 510060, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Affiliated Hosp 1, Ctr HepatoPancreat Biliary Surg, Guangzhou 510080, Guangdong, Peoples R China
[4] Sun Yat Sen Univ, Affiliated Hosp 1, Guangdong Prov Key Lab Brain Funct & Dis, Dept Neurosurg,Guangdong Translat Med Innovat Pla, Guangzhou 510080, Guangdong, Peoples R China
[5] Sun Yat Sen Univ, Canc Ctr, Dept Surg, Guangzhou 510060, Guangdong, Peoples R China
[6] Sun Yat Sen Univ, Canc Ctr, Dept Nasopharyngeal Carcinoma, Guangzhou 510060, Guangdong, Peoples R China
[7] Shandong First Med Univ, Shandong Canc Hosp & Inst, Dept Radiat Oncol, Jinan 250117, Shandong, Peoples R China
[8] Shandong Acad Med Sci, Jinan 250117, Shandong, Peoples R China
[9] Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Thorac Surg, Guangzhou 510080, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Hepatocellular carcinoma; circMAP3K4; N6-methyadenosine; Translation; AIF; MIB1; CIRCULAR RNAS; CELL-DEATH; TRANSLATION; AIF; CHEMOTHERAPY; CISPLATIN; DATABASE; CIRCRNA;
D O I
10.1186/s12943-022-01537-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background Circular RNAs (circRNAs) regulate various biological activities and have been shown to play crucial roles in hepatocellular carcinoma (HCC) progression. However, only a few coding circRNAs have been identified in cancers, and their roles in HCC remain elusive. This study aimed to identify coding circRNAs and explore their function in HCC. Methods CircMAP3K4 was selected from the CIRCpedia database. We performed a series of experiments to determine the characteristics and coding capacity of circMAP3K4. We then used in vivo and in vitro assays to investigate the biological function and mechanism of circMAP3K4 and its protein product, circMAP3K4-455aa, in HCC. Results We found circMAP3K4 to be an upregulated circRNA with coding potential in HCC. IGF2BP1 recognized the circMAP3K4 N6-methyladenosine modification and promoted its translation into circMAP3K4-455aa. Functionally, circMAP3K4-455aa prevented cisplatin-induced apoptosis in HCC cells by interacting with AIF, thus protecting AIF from cleavage and decreasing its nuclear distribution. Moreover, circMAP3K4-455aa was degraded through the ubiquitin-proteasome E3 ligase MIB1 pathway. Clinically, a high level of circMAP3K4 is an independent prognostic factor for adverse overall survival and adverse disease-free survival of HCC patients. Conclusions CircMAP3K4 is a highly expressed circRNA in HCC. Driven by m6A modification, circMAP3K4 encoded circMAP3K4-455aa, protected HCC cells from cisplatin exposure, and predicted worse prognosis of HCC patients. Targeting circMAP3K4-455aa may provide a new therapeutic strategy for HCC patients, especially for those with chemoresistance.
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页数:16
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