Evidence map›Paper›PMID 34465388›Full record

ArticleCell & bioscience2021

Long noncoding RNA SNHG1 promotes TERT expression by sponging miR-18b-5p in breast cancer.

Yujuan Kang, Lin Wan, Qin Wang, Yanling Yin, Jiena Liu, Lei Liu, Hao Wu, Lei Zhang, Xin Zhang, Shouping Xu and 1 more

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Cell & bioscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 35% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Yujuan Kang *Department of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China.
Lin Wan *Department of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China.
Qin WangDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China.
Yanling YinDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China.
Jiena LiuDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China.
Lei LiuDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China.
Hao WuDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China.
Lei ZhangDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China.
Xin ZhangDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China.
Shouping XuDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China. Shoupingxu@hrbmu.edu.cn.
Da PangDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150040, China. pangda@ems.hrbmu.edu.cn.ORCID http://orcid.org/0000-0003-2853-4170
Harbin Medical University · CN

Funding

National Natural Science Foundation of China 81972706National Natural Science Foundation of China 82072904
6 · The paper itself

Abstract

backgroundLong noncoding RNA (lncRNA) small nucleolar RNA host gene 1 (SNHG1) plays a positive role in the progression of human malignant tumors. However, the molecular mechanism of SNHG1 remains elusive in breast cancer.

resultsLncRNA SNHG1 was upregulated and had a positive relationship with poor prognosis according to bioinformatics analysis in pan-cancer including breast cancer. Silencing SNHG1 inhibited tumorigenesis in breast cancer both in vitro and in vivo. Mechanistically, SNHG1 functioned as a competing endogenous RNA (ceRNA) to promote TERT expression by sponging miR-18b-5p in breast cancer. miR-18b-5p acted as a tumor repressor in breast cancer. Moreover, the combination of SNHG1 knockdown and TERT inhibitor administration showed a synergistic inhibitory effect on breast cancer growth in vivo. Finally, E2F1 as a transcription factor, binding to SNHG1 promoter and enhanced SNHG1 transcription in breast cancer.

conclusionsOur results provide a comprehensive understanding of the oncogenic mechanism of lncRNA SNHG1 in breast cancer. Importantly, we identified a novel E2F1-SNHG1-miR-18b-5p-TERT axis, which may be a potential therapeutic target for breast cancer. Our results also provided a potential treatment for breast cancer when knockdown SNHG1 and TERT inhibitor administration simultaneously.

Indexed as

Breast cancerCompeting endogenous RNAE2F1SNHG1TERT

Identifiers

PMID34465388
PMCPMC8407068
OpenAlexW3134824709

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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.