Restoration of 5-hydroxymethylcytosine by ascorbate blocks kidney tumour growth

被引:41
作者
Ge, Guangzhe [1 ,2 ]
Peng, Ding [1 ,3 ,4 ,5 ]
Xu, Ziying [1 ,2 ]
Guan, Bao [3 ,4 ,5 ]
Xin, Zijuan [1 ,2 ]
He, Qun [3 ,4 ,5 ]
Zhou, Yuanyuan [1 ]
Li, Xuesong [3 ,4 ,5 ]
Zhou, Liqun [3 ,4 ,5 ]
Ci, Weimin [1 ,2 ]
机构
[1] Chinese Acad Sci, Key Lab Genom & Precis Med, Beijing Inst Genom, Beijing, Peoples R China
[2] Univ Chinese Acad Sci, Beijing, Peoples R China
[3] Peking Univ, Dept Urol, Hosp 1, Beijing, Peoples R China
[4] Peking Univ, Inst Urol, Beijing, Peoples R China
[5] Natl Urol Canc Ctr, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
5-hydroxymethylcytosine; clear-cell renal cell carcinoma; differentiation; epigenetic reprogramming; vitamin C; MEDIATED 5-METHYLCYTOSINE OXIDATION; I CLINICAL-TRIAL; DOSE VITAMIN-C; PHARMACOLOGICAL ASCORBATE; SUPPLEMENTAL ASCORBATE; SUPPORTIVE TREATMENT; DNA DEMETHYLATION; ADVANCED CANCER; SURVIVAL TIMES; SELF-RENEWAL;
D O I
10.15252/embr.201745401
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
Loss of 5-hydroxymethylcytosine (5hmC) occurs frequently in a wide variety of tumours, including clear-cell renal cell carcinoma (ccRCC). It remains unknown, however, whether the restoration of 5hmC patterns in tumours could have therapeutic efficacy. Here, we used sodium L-ascorbate (vitamin C, AsANa) and the oxidation-resistant form L-ascorbic acid 2-phosphate sesquimag-nesium (APM) for the restoration of 5hmC patterns in ccRCC cells. At physiological concentrations, both show anti-tumour efficacy during long-term treatment in vitro and in vivo. Strikingly, global 5hmC patterns in ccRCC cells after treatment resemble those of normal kidney tissue, which is observed also in treated xenograft tumours, and in primary cells from a ccRCC patient. Further, RNA-seq data show that long-term treatment with vitamin C changes the transcriptome of ccRCC cells. Finally, APM treatment induces less non-specific cell damage and shows increased stability in mouse plasma compared to AsANa. Taken together, our study provides proof of concept for an epigenetic differentiation therapy of ccRCC with vitamin C, especially APM, at low doses by 5hmC reprogramming.
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页数:14
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