Evidence map›Paper›PMID 36316314›Full record

ArticleCell death discovery2022

NOP53 undergoes liquid-liquid phase separation and promotes tumor radio-resistance.

Jie Shi, Si-Ying Chen, Xiao-Ting Shen, Xin-Ke Yin, Wan-Wen Zhao, Shao-Mei Bai, Wei-Xing Feng, Li-Li Feng, Caolitao Qin, Jian Zheng and 2 more

Abstract read
In one paragraph

Article in Cell death discovery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

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  12. Ubiquitin-induced RNF168 condensation promotes DNA double-strand break repair.Proceedings of the National Academy of Sciences of the United States of America · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Jie Shi *Department of Radiation Oncology, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, 510655, P.R. China.
Si-Ying Chen *Guangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, 510655, P.R. China.
Xiao-Ting Shen *Center for Reproductive Medicine and Department of Gynecology & Obstetrics, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, P.R. China.
Xin-Ke YinGuangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, 510655, P.R. China.
Wan-Wen ZhaoGuangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, 510655, P.R. China.
Shao-Mei BaiGuangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, 510655, P.R. China.
Wei-Xing FengGuangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, 510655, P.R. China.
Li-Li FengGuangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, 510655, P.R. China.
Caolitao QinDepartment of Radiation Oncology, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, 510655, P.R. China.
Jian ZhengDepartment of Radiation Oncology, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, 510655, P.R. China.
Yun-Long WangDepartment of Radiation Oncology, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, 510655, P.R. China. wangylong7@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0002-5925-6938
Xin-Juan FanGuangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, 510655, P.R. China. fanxjuan@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0002-1843-9447

Funding

China Postdoctoral Science Foundation 2020M680138Guangdong Science and Technology Department (Science and Technology Department, Guangdong Province) 2020A1515010314Guangdong Science and Technology Department (Science and Technology Department, Guangdong Province) 2022A1515012363National Natural Science Foundation of China (National Science Foundation of China) 82103770National Natural Science Foundation of China (National Science Foundation of China) 82122057National Natural Science Foundation of China (National Science Foundation of China) 82171163Natural Science Foundation of Guangdong Province (Guangdong Natural Science Foundation) 2019A1515010901Natural Science Foundation of Guangdong Province (Guangdong Natural Science Foundation) 2019B030316003Natural Science Foundation of Guangdong Province (Guangdong Natural Science Foundation) 2021B1515020022
6 · The paper itself

Abstract

Aberrant DNA damage response (DDR) axis remains the major molecular mechanism for tumor radio-resistance. We recently characterized liquid-liquid phase separation (LLPS) as an essential mechanism of DDR, and identified several key DDR factors as potential LLPS proteins, including nucleolar protein NOP53. In this study, we found that NOP53 formed highly concentrated droplets in vivo and in vitro, which had liquid-like properties including the fusion of adjacent condensates, rapid fluorescence recovery after photobleaching and the sensitivity to 1,6-hexanediol. Moreover, the intrinsically disordered region 1 (IDR1) is required for NOP53 phase separation. In addition, multivalent-arginine-rich linear motifs (M-R motifs), which are enriched in NOP53, were essential for its nucleolar localization, but were dispensable for the LLPS of NOP53. Functionally, NOP53 silencing diminished tumor cell growth, and significantly sensitized colorectal cancer (CRC) cells to radiotherapy. Mechanically, NOP53 negatively regulated p53 pathway in CRC cells treated with or without radiation. Importantly, data from clinical samples confirmed a correlation between NOP53 expression and tumor radio-resistance. Together, these results indicate an important role of NOP53 in radio-resistance, and provide a potential target for tumor radio-sensitization.

Identifiers

PMID36316314
PMCPMC9622906

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.