Evidence map›Paper›PMID 22341523›Full record

ArticleThe American journal of pathology2012

Role of ERRF, a novel ER-related nuclear factor, in the growth control of ER-positive human breast cancer cells.

Dan Su, Xiaoying Fu, Songqing Fan, Xiao Wu, Xin-Xin Wang, Liya Fu, Xue-Yuan Dong, Jianping Jenny Ni, Li Fu, Zhengmao Zhu and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

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  10. Coamplification ofProceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  11. Article
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  13. Association of estrogen receptor-α A908G (K303R) mutation with breast cancer risk.International journal of clinical and experimental medicine · 2013
    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 4 institutions in 2 countries.

Dan SuDepartment of Genetics and Cell Biology, Nankai University College of Life Sciences, Tianjin, China.
Xiaoying FuDepartment of Hematology and Medical Oncology, School of Medicine, Winship Cancer Institute, Emory University, Atlanta, Georgia.
Songqing FanDepartment of Pathology, Second Xiangya Hospital, Central South University, Hunan, China.
Xiao WuDepartment of Genetics and Cell Biology, Nankai University College of Life Sciences, Tianjin, China.
Xin-Xin WangKey Laboratory of Breast Cancer Research, Department of Breast Cancer Pathology and Research Laboratory, Cancer Hospital of Tianjin Medical University, Tianjin, China.
Liya FuDepartment of Genetics and Cell Biology, Nankai University College of Life Sciences, Tianjin, China.
Xue-Yuan DongDepartment of Hematology and Medical Oncology, School of Medicine, Winship Cancer Institute, Emory University, Atlanta, Georgia.
Jianping Jenny NiDepartment of Hematology and Medical Oncology, School of Medicine, Winship Cancer Institute, Emory University, Atlanta, Georgia.
Li FuKey Laboratory of Breast Cancer Research, Department of Breast Cancer Pathology and Research Laboratory, Cancer Hospital of Tianjin Medical University, Tianjin, China. Electronic address: fuli@tijmu.edu.cn.
Zhengmao ZhuDepartment of Genetics and Cell Biology, Nankai University College of Life Sciences, Tianjin, China. Electronic address: zhuzhengmao@nankai.edu.cn.
Jin-Tang DongDepartment of Genetics and Cell Biology, Nankai University College of Life Sciences, Tianjin, China; Department of Hematology and Medical Oncology, School of Medicine, Winship Cancer Institute, Emory University, Atlanta, Georgia. Electronic address: jtdong@nankai.edu.cn.
Nankai University · CNEmory University · USTianjin Medical University Cancer Institute and Hospital · CNCentral South University · CN

Funding

MOLECULAR DISSECTION OF 13Q14 IN PROSTATE CANCERR01CA085560 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI DONG, JIN-TANG · 2000 to 2010
$2.5M
NCI NIH HHS R01 CA085560NCI NIH HHS R01CA085560
6 · The paper itself

Abstract

Whereas estrogen-estrogen receptor α (ER) signaling plays an important role in breast cancer growth, it is also necessary for the differentiation of normal breast epithelial cells. How this functional conversion occurs, however, remains unknown. Based on a genome-wide sequencing study that identified mutations in several breast cancer genes, we examined some of the genes for mutations, expression levels, and functional effects on cell proliferation and tumorigenesis. We present the data for C1orf64 or ER-related factor (ERRF) from 31 cell lines and 367 primary breast cancer tumors. Whereas mutation of ERRF was infrequent (1 of 79 or 1.3%), its expression was up-regulated in breast cancer, and the up-regulation was more common in lower-stage tumors. In addition, increased ERRF expression was significantly associated with ER and/or progesterone receptor (PR) positivity, which was still valid in human epidermal growth factor receptor 2 (HER2)-negative tumors. In ER-positive tumors, ERRF expression was inversely correlated with HER2 status. Furthermore, higher ERRF protein expression was significantly associated with better disease-free survival and overall survival, particularly in ER- and/or PR-positive and HER2-negative tumors (luminal A subtype). Functionally, knockdown of ERRF in two ER-positive breast cancer cell lines, T-47D and MDA-MB-361, suppressed cell growth in vitro and tumorigenesis in xenograft models. These results suggest that ERRF plays a role in estrogen-ER-mediated growth of breast cancer cells and could, thus, be a potential therapeutic target.

Indexed as

AdultAgedAnimalsBreast NeoplasmsCell Line, TumorEstrogen Receptor alphaFemaleGene Knockdown TechniquesGenes, erbB-2HumansMiceMice, Inbred BALB CMice, NudeMiddle AgedNeoplasm TransplantationNuclear ProteinsESR1 protein, humanEstrogen Receptor alphaNuclear ProteinsRNA, Small InterferingSRARP protein, human

Identifiers

PMID22341523
PMCPMC3349889
OpenAlexW2045585997

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.