Evidence map›Paper›PMID 34589276›Full record

ArticleMolecular therapy. Nucleic acids2021

ERα determines the chemo-resistant function of mutant p53 involving the switch between lincRNA-p21 and DDB2 expressions.

Yu-Hao He, Ming-Hsin Yeh, Hsiao-Fan Chen, Tsu-Shing Wang, Ruey-Hong Wong, Ya-Ling Wei, Thanh Kieu Huynh, Dai-Wei Hu, Fang-Ju Cheng, Jhen-Yu Chen and 10 more

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

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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

20 authors at 4 institutions in 1 country.

Yu-Hao HeThe PhD Program for Cancer Biology and Drug Discovery, China Medical University and Academia Sinica, Taichung 40402, Taiwan.
Ming-Hsin YehDepartment of Surgery, Chung Shan Medical University Hospital, Taichung 40201, Taiwan.
Hsiao-Fan ChenCenter for Molecular Medicine, China Medical University Hospital, Taichung 40402, Taiwan.
Tsu-Shing WangDepartment of Biomedical Sciences, Chung Shan Medical University, Taichung 40201, Taiwan.
Ruey-Hong WongDepartment of Public Health, Chung Shan Medical University, Taichung 40201, Taiwan.
Ya-Ling WeiCenter for Molecular Medicine, China Medical University Hospital, Taichung 40402, Taiwan.
Thanh Kieu HuynhCenter for Molecular Medicine, China Medical University Hospital, Taichung 40402, Taiwan.
Dai-Wei HuCenter for Molecular Medicine, China Medical University Hospital, Taichung 40402, Taiwan.
Fang-Ju ChengCenter for Molecular Medicine, China Medical University Hospital, Taichung 40402, Taiwan.
Jhen-Yu ChenCenter for Molecular Medicine, China Medical University Hospital, Taichung 40402, Taiwan.
Shu-Wei HuCenter for Molecular Medicine, China Medical University Hospital, Taichung 40402, Taiwan.
Chia-Chen HuangDepartment of Public Health, Chung Shan Medical University, Taichung 40201, Taiwan.
Yeh ChenDrug Development Center, China Medical University, Taichung 40402, Taiwan.
Jiaxin YuAI Innovation Center, China Medical University Hospital, Taiwan 40402, Taiwan.
Wei-Chung ChengThe PhD Program for Cancer Biology and Drug Discovery, China Medical University and Academia Sinica, Taichung 40402, Taiwan.
Pei-Chun ShenResearch Center for Cancer Biology, China Medical University, Taichung 40402, Taiwan.
Liang-Chih LiuDivision of Breast Surgery, China Medical University Hospital, Taichung 40402, Taiwan.
Chih-Hao HuangDivision of Breast Surgery, China Medical University Hospital, Taichung 40402, Taiwan.
Ya-Jen ChangThe PhD Program for Cancer Biology and Drug Discovery, China Medical University and Academia Sinica, Taichung 40402, Taiwan.
Wei-Chien HuangThe PhD Program for Cancer Biology and Drug Discovery, China Medical University and Academia Sinica, Taichung 40402, Taiwan.
China Medical University · TWChung Shan Medical University Hospital · TWAsia University · TWChung Shan Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutant p53 (mutp53) commonly loses its DNA binding affinity to p53 response elements (p53REs) and fails to induce apoptosis fully. However, the p53 mutation does not predict chemoresistance in all subtypes of breast cancers, and the critical determinants remain to be identified. In this study, mutp53 was found to mediate chemotherapy-induced long intergenic noncoding RNA-p21 (lincRNA-p21) expression by targeting the G-quadruplex structure rather than the p53RE on its promoter to promote chemosensitivity. However, estrogen receptor alpha (ERα) suppressed mutp53-mediated lincRNA-p21 expression by hijacking mutp53 to upregulate damaged DNA binding protein 2 (

Indexed as

chemotherapyDDB2estrogen receptorG-quadruplexlincRNA-p21mutant p53

Identifiers

PMID34589276
PMCPMC8463322
OpenAlexW3190630403

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.