Long non-coding RNA TILR constitutively represses TP53 and apoptosis in lung cancer

被引:8
作者
Iwai, Mika [1 ]
Kajino, Taisuke [1 ,2 ]
Nakatochi, Masahiro [3 ]
Yanagisawa, Kiyoshi [1 ,4 ]
Hosono, Yasuyuki [5 ,6 ]
Isomura, Hisanori [1 ,2 ]
Shimada, Yukako [1 ,2 ]
Suzuki, Motoshi [1 ,7 ]
Taguchi, Ayumu [2 ,8 ]
Takahashi, Takashi [1 ,9 ]
机构
[1] Nagoya Univ, Ctr Neurol Dis & Canc, Div Mol Carcinogenesis, Grad Sch Med, Nagoya 4668550, Japan
[2] Aichi Canc Ctr, Div Mol Diagnost, Res Inst, Nagoya 4648681, Japan
[3] Nagoya Univ, Dept Integrated Hlth Sci, Publ Hlth Informat Unit, Grad Sch Med, Nagoya 4618673, Japan
[4] Meijo Univ, Fac Pharm, Dept Mol & Canc Med, Nagoya 4688502, Japan
[5] Aichi Canc Ctr, Div Mol Therapeut, Res Inst, Nagoya 4648681, Japan
[6] Okayama Univ, Dept Pharmacol, Grad Sch Med Dent & Pharmaceut Sci, Okayama 7008558, Japan
[7] Fujita Hlth Univ, Sch Med, Dept Mol Oncol, Toyoake 4701192, Japan
[8] Nagoya Univ, Dept Canc Diagnost & Therapeut, Div Adv Canc Diagnost, Grad Sch Med, Nagoya 4648681, Japan
[9] Aichi Canc Ctr, Nagoya 4648681, Japan
基金
日本学术振兴会;
关键词
FANCONI-ANEMIA; P53; ADENOCARCINOMA; EXPRESSION; PROTEINS; CLASSIFICATION; ASSOCIATION; TRANSLATION;
D O I
10.1038/s41388-022-02546-w
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
Non-coding RNAs have an integral regulatory role in numerous functions related to lung cancer development. Here, we report identification of a novel lncRNA, termed TP53-inhibitinglncRNA (TILR), which was found to function as a constitutive negative regulator of p53 expression, including activation of downstream genes such as p21 and MDM2, and induction of apoptosis. A proteomic search for TILR-associated proteins revealed an association with PCBP2, while the mid-portion of TILR was found to be required for both PCBP2 and p53 mRNA binding. In addition, depletion of PCBP2 resulted in phenocopied effects of TILR silencing. TILR was also shown to suppress p53 expression in a post-transcriptional manner, as well as via a positive feedback loop involving p53 and Fanconi anemia pathway genes. Taken together, the present findings clearly demonstrate that TILR constitutively inhibits p53 expression in cooperation with PCBP2, thus maintaining p53 transcriptional activity at a level sufficiently low for avoidance of spurious apoptosis induction.
引用
收藏
页码:364 / 373
页数:10
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