Evidence map›Paper›PMID 28264987›Full record

ArticleEMBO reports2017

Nuclear retention of the lncRNA SNHG1 by doxorubicin attenuates hnRNPC-p53 protein interactions.

Yuan Shen, Shanshan Liu, Jiao Fan, Yinghua Jin, Baolei Tian, Xiaofei Zheng, Hanjiang Fu

Open access · bronzeAbstract read
In one paragraph

Article in EMBO reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
3.6field-weighted citation impact, top 6% of its field
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

66 citing papers in PubMed, 117 citations in OpenAlex.

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  16. LncRNA Fendrr: involvement in the protective role of nucleolin against HRedox report : communications in free radical research · 2023
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6 more citing papers are in PubMed but not listed here.

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

7 authors at 3 institutions in 1 country.

Yuan ShenBeijing Key Laboratory for Radiobiology, Beijing Institute of Radiation Medicine, Beijing, China.
Shanshan LiuBeijing Key Laboratory for Radiobiology, Beijing Institute of Radiation Medicine, Beijing, China.
Jiao FanBeijing Key Laboratory for Radiobiology, Beijing Institute of Radiation Medicine, Beijing, China.
Yinghua JinKey Laboratory for Molecular Enzymology and Engineering (The Ministry of Education), College of Life Sciences, Jilin University, Changchun, Jilin, China yhjin@jlu.edu.cn xfzheng100@126.com fuhj75@126.com.ORCID 0000-0002-7385-9903
Baolei TianBeijing Key Laboratory for Radiobiology, Beijing Institute of Radiation Medicine, Beijing, China.
Xiaofei ZhengBeijing Key Laboratory for Radiobiology, Beijing Institute of Radiation Medicine, Beijing, China yhjin@jlu.edu.cn xfzheng100@126.com fuhj75@126.com.ORCID 0000-0001-6032-729X
Hanjiang FuBeijing Key Laboratory for Radiobiology, Beijing Institute of Radiation Medicine, Beijing, China yhjin@jlu.edu.cn xfzheng100@126.com fuhj75@126.com.ORCID 0000-0002-4352-1178
Beijing Radiation Center · CNJilin University · CNChinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The protein p53 plays a crucial role in the regulation of cellular responses to diverse stresses. Thus, a major priority in cell biology is to define the mechanisms that regulate p53 activity in response to stresses or maintain it at basal levels under normal conditions. Moreover, further investigation is required to establish whether RNA participates in regulating p53's interaction with other proteins. Here, by conducting systematic experiments, we discovered a p53 interactor-hnRNPC-that directly binds to p53, destabilizes it, and prevents its activation under normal conditions. Upon doxorubicin treatment, the lncRNA SNHG1 is retained in the nucleus through its binding with nucleolin and it competes with p53 for hnRNPC binding, which upregulates p53 levels and promotes p53-dependent apoptosis by impairing hnRNPC regulation of p53 activity. Our results indicate that a balance between lncRNA SNHG1 and hnRNPC regulates p53 activity and p53-dependent apoptosis upon doxorubicin treatment, and further indicate that a change in lncRNA subcellular localization under specific circumstances is biologically significant.

Indexed as

ApoptosisCarrier ProteinsCell Line, TumorCell NucleusDoxorubicinHeterogeneous-Nuclear Ribonucleoprotein Group CHumansModels, BiologicalNucleotide MotifsProtein BindingProtein StabilityRNA, Long NoncodingRNA TransportTumor Suppressor Protein p53Carrier ProteinsDoxorubicinHeterogeneous-Nuclear Ribonucleoprotein Group CHNRNPC protein, humanlong non-coding RNA SNHG1, humanRNA, Long NoncodingTumor Suppressor Protein p53doxorubicinhnRNPClncRNAp53SNHG1

Identifiers

PMID28264987
PMCPMC5376760
OpenAlexW2594230179

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.