Evidence map›Paper›PMID 35568705›Full record

ArticleCell death discovery2022

CircEIF3H-IGF2BP2-HuR scaffold complex promotes TNBC progression via stabilizing HSPD1/RBM8A/G3BP1 mRNA.

Xiaojin Song, Bing Chen, Yiran Liang, Yaming Li, Hanwen Zhang, Dianwen Han, Yajie Wang, Fangzhou Ye, Lijuan Wang, Wenjing Zhao and 1 more

Abstract read
In one paragraph

Article in Cell death discovery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

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  17. [Circular RNA circRSF1 binds to HuR to promote radiation-induced inflammatory phenotype in hepatic stellate cells].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2023
    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.

Xiaojin Song *Department of Breast Surgery, Qilu Hospital of Shandong University, Jinan, Shandong Province, 250012, China.
Bing Chen *Pathology Tissue Bank, Qilu Hospital of Shandong University, Jinan, Shandong Province, 250012, China.
Yiran LiangDepartment of Breast Surgery, Qilu Hospital of Shandong University, Jinan, Shandong Province, 250012, China.
Yaming LiDepartment of Breast Surgery, Qilu Hospital of Shandong University, Jinan, Shandong Province, 250012, China.
Hanwen ZhangDepartment of Breast Surgery, Qilu Hospital of Shandong University, Jinan, Shandong Province, 250012, China.
Dianwen HanDepartment of Breast Surgery, Qilu Hospital of Shandong University, Jinan, Shandong Province, 250012, China.
Yajie WangDepartment of Breast Surgery, Qilu Hospital of Shandong University, Jinan, Shandong Province, 250012, China.
Fangzhou YeDepartment of Breast Surgery, Qilu Hospital of Shandong University, Jinan, Shandong Province, 250012, China.
Lijuan WangPathology Tissue Bank, Qilu Hospital of Shandong University, Jinan, Shandong Province, 250012, China.
Wenjing ZhaoPathology Tissue Bank, Qilu Hospital of Shandong University, Jinan, Shandong Province, 250012, China.
Qifeng YangDepartment of Breast Surgery, Qilu Hospital of Shandong University, Jinan, Shandong Province, 250012, China. qifengy_sdu@163.com.ORCID http://orcid.org/0000-0003-0576-8513

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81874119
6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) is a molecular subtype with an unfavorable prognosis, and metastasis is the main reason for the failure of clinical treatment. However, the expression profile and regulatory function of circRNAs in TNBC progression are not fully understood. Herein, we performed high-throughput RNA-seq in paired breast cancer tissues and adjacent normal tissues and discovered a novel circRNA, circEIF3H, which was upregulated in breast cancer tissues. Large cohort survival analysis confirmed the association between high circEIF3H expression and poor prognosis of TNBC, indicating the vital function of circEIF3H in TNBC progression. Then we conducted both in vitro and in vivo experiments which illustrated that circEIF3H was essential for TNBC proliferation and metastasis. Further experiments showed that circEIF3H did not function as a microRNA sponge as in the most well-established pathway, but as a scaffold for IGF2BP2 and HuR to regulate the mRNA stability of HSPD1, RBM8A, and G3BP1. Our findings provide insight into a novel circRNA, circEIF3H, with significant cancer-promoting function via serving as a scaffold for IGF2BP2/HuR. These results identified circEIF3H as a potential target for developing individualized therapy of TNBC in the approaching future.

Identifiers

PMID35568705
PMCPMC9107465

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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.