Evidence map›Paper›PMID 25881544›Full record

ArticleOncotarget2015

Estrogen receptor (ER) was regulated by RNPC1 stabilizing mRNA in ER positive breast cancer.

Liang Shi, Tian-Song Xia, Xiao-Long Wei, Wenbin Zhou, Jinqiu Xue, Lin Cheng, Peipei Lou, Chunlian Li, Ying Wang, Ji-Fu Wei and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
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  4. RBM38 in cancer: role and mechanism.Cellular and molecular life sciences : CMLS · 2021
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  10. RBMS2 inhibits the proliferation by stabilizing P21 mRNA in breast cancer.Journal of experimental & clinical cancer research : CR · 2018
    Article
  11. Genetic Ablation ofCancer research · 2018
    Article
  12. Article
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  14. The role of c-Myc-RBM38 loop in the growth suppression in breast cancer.Journal of experimental & clinical cancer research : CR · 2017
    Article
  15. Article
  16. Article
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

11 authors at 2 institutions in 1 country.

Liang ShiJiangsu Breast Disease Center, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.
Tian-Song XiaJiangsu Breast Disease Center, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.
Xiao-Long WeiDepartment of Pathology, Cancer Hospital of Shantou University Medical College, Shantou, China.
Wenbin ZhouJiangsu Breast Disease Center, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.
Jinqiu XueJiangsu Breast Disease Center, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.
Lin ChengJiangsu Breast Disease Center, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.
Peipei LouJiangsu Breast Disease Center, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.
Chunlian LiJiangsu Breast Disease Center, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.
Ying WangJiangsu Breast Disease Center, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.
Ji-Fu WeiResearch Division of Clinical Pharmacology, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.
Qiang DingJiangsu Breast Disease Center, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.
Nanjing Medical University · CNShantou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Estrogen receptors (ERs), including ERα and ERβ, mainly mediate the genotype effect of estrogen. ERα is highly expressed in most breast cancers. Endocrine therapy is the most effective and safety adjunctive therapy for ER positive breast cancers. RNPC1, an RNA binding protein (RBP), post-transcriptionally regulating gene expression, is emerging as a critical mechanism for gene regulation in mammalian cells. In this study, we revealed RNPC1's capability of regulating ERα expression. There was a significant correlation between RNPC1 and ERα expression in breast cancer tissues. Ectopic expression of RNPC1 could increase ERα transcript and expression in breast cancer cells, and vice versa. Consistent with this, RNPC1 was able to bind to ERα transcript to increase its stability. Furthermore, overexpression of ERα could decrease the level of RNPC1 transcript and protein. It suggested a novel mechanism by which ERα expression was regulated via stabilizing mRNA. A regulatory feedback loop between RNPC1 and ERα was proved. It indicated that RNPC1 played a crucial role in ERα regulation in ER-positive breast cancers via binding to ERα mRNA. These findings might provide new insights into breast cancer endocrine therapy and ERα research.

Indexed as

Breast NeoplasmsCell Line, TumorFemaleHumansReceptors, EstrogenRNA-Binding ProteinsRNA, MessengerReceptors, EstrogenRNA-Binding ProteinsRNA, Messengerbreast cancerestrogen receptormRNA stabilityRNPC1

Identifiers

PMID25881544
PMCPMC4494937
OpenAlexW1792229374

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.