Evidence map›Paper›PMID 28337281›Full record

ArticleAmerican journal of translational research2017

C-MYC-induced upregulation of lncRNA SNHG12 regulates cell proliferation, apoptosis and migration in triple-negative breast cancer.

Ouchen Wang, Fan Yang, Yehuan Liu, Lin Lv, Ruimin Ma, Chuanzhi Chen, Jiao Wang, Qiufan Tan, Yue Cheng, Erjie Xia and 2 more

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 1 pooled it
7.4field-weighted citation impact, top 1% 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

80 citing papers in PubMed, 1 synthesis or guideline pooled it, 163 citations in OpenAlex.

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20 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

12 authors at 2 institutions in 1 country.

Ouchen WangDepartment of Surgical Oncology, The First Affiliated Hospital of Wenzhou Medical University Wenzhou, Zhejiang, PR China.
Fan YangDepartment of Surgical Oncology, The First Affiliated Hospital of Wenzhou Medical University Wenzhou, Zhejiang, PR China.
Yehuan LiuDepartment of Surgical Oncology, The First Affiliated Hospital of Wenzhou Medical University Wenzhou, Zhejiang, PR China.
Lin LvDepartment of Oncology, Jinhua Municipal Central Hospital Jinhua, Zhejiang, PR China.
Ruimin MaDepartment of Breast Surgery, The Second Affiliated Hospital of Wenzhou Medical University Wenzhou, Zhejiang, PR China.
Chuanzhi ChenDepartment of Surgical Oncology, The First Affiliated Hospital of Wenzhou Medical University Wenzhou, Zhejiang, PR China.
Jiao WangDepartment of Eye Hospital, Wenzhou Medical University Wenzhou, Zhejiang, PR China.
Qiufan TanDepartment of Eye Hospital, Wenzhou Medical University Wenzhou, Zhejiang, PR China.
Yue ChengDepartment of Surgical Oncology, The First Affiliated Hospital of Wenzhou Medical University Wenzhou, Zhejiang, PR China.
Erjie XiaDepartment of Surgical Oncology, The First Affiliated Hospital of Wenzhou Medical University Wenzhou, Zhejiang, PR China.
Yizuo ChenDepartment of Surgical Oncology, The First Affiliated Hospital of Wenzhou Medical University Wenzhou, Zhejiang, PR China.
Xiaohua ZhangDepartment of Surgical Oncology, The First Affiliated Hospital of Wenzhou Medical University Wenzhou, Zhejiang, PR China.
Wenzhou Medical University · CNJinhua Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) is one of the most aggressive subtypes of breast cancer, with a significantly higher recurrence and mortality rate. There is an urgent need to uncover the mechanism underlying TNBC and establish therapeutic targets. Long non-coding RNAs (lncRNAs) are involved in a series of biological functions and provide novel insights into the molecular mechanism of cancer. Based on their expression specificity and large number, lncRNAs are likely to serve as the basis for clinical applications in oncology. In our previous study, we utilized RNA sequencing (RNA-seq) to explore the lncRNAs expression profiles in TNBC and identified that small nucleolar RNA host gene 12 (SNHG12) was remarkably increased in TNBC. However, the role of SNHG12 in TNBC has not been clarified. Herein, we determine that SNHG12 is upregulated in TNBC, and its high expression is significantly correlated with tumor size and lymph node metastasis. Mechanistic investigations show that SNHG12 is a direct transcriptional target of c-MYC. Silencing SNHG12 expression inhibits TNBC cells proliferation and apoptosis promotion, whereas SNHG12 overexpression has the opposite effect. In addition, we reveal that SNHG12 may promote cells migration by regulating MMP13 expression. To the best of our knowledge, it is the first report indicating that SNHG12 is involved in breast cancer. Taken together, our findings suggest that SNHG12 contributes to the oncogenic potential of TNBC and may be a promising therapeutic target.

Indexed as

c-MYCLong non-coding RNASNHG12triple-negative breast cancer

Identifiers

PMID28337281
PMCPMC5340688
OpenAlexW2919361804

What OpenQuestion holds

Textmetadata
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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.