Details

Autor(en) / Beteiligte

• Wang, Yanying
• Wang, Jing
• Li, Xiaoyu
• Xiong, Xushen
• Wang, Jianyi
• Zhou, Ziheng
• Zhu, Xiaoxiao
• Gu, Yang
• Dominissini, Dan
• He, Lei
• Tian, Yong
• Yi, Chengqi
• Fan, Zusen

Titel

N1-methyladenosine methylation in tRNA drives liver tumourigenesis by regulating cholesterol metabolism

Ist Teil von

• Nature communications, 2021-11, Vol.12 (1), p.6314-6314, Article 6314

Ort / Verlag

London: Nature Publishing Group

Erscheinungsjahr

2021

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• Abstract Hepatocellular carcinoma (HCC) accounts for the majority of primary liver cancers and is characterized by high recurrence and heterogeneity, yet its mechanism is not well understood. Here we show that N 1 -methyladenosine methylation (m 1 A) in tRNA is remarkably elevated in hepatocellular carcinoma (HCC) patient tumour tissues. Moreover, m 1 A methylation signals are increased in liver cancer stem cells (CSCs) and are negatively correlated with HCC patient survival. TRMT6 and TRMT61A, forming m 1 A methyltransferase complex, are highly expressed in advanced HCC tumours and are negatively correlated with HCC survival. TRMT6/TRMT61A-mediated m 1 A methylation is required for liver tumourigenesis. Mechanistically, TRMT6/TRMT61A elevates the m 1 A methylation in a subset of tRNA to increase PPARδ translation, which in turn triggers cholesterol synthesis to activate Hedgehog signaling, eventually driving self-renewal of liver CSCs and tumourigenesis. Finally, we identify a potent inhibitor against TRMT6/TRMT61A complex that exerts effective therapeutic effect on liver cancer.