Evidence map›Paper›PMID 34006305›Full record

ArticleDiagnostic pathology2021

A novel tumor suppressor ASMTL-AS1 regulates the miR-1228-3p/SOX17/β-catenin axis in triple-negative breast cancer.

Jie Sun, Xiaohua Li, Enqiao Yu, Jianxia Liu, Liang Sun, Qin He, Qiran Lu

Open access · goldAbstract read
In one paragraph

Article in Diagnostic pathology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Jie Sun *Department of Breast Surgery, The 1st Affiliated Hospital of Soochow University, Ward 6, 2F Surgical Building, 188 Shizi Street, Gusu District, Jiangsu, 215006, Suzhou, China.
Xiaohua Li *Department of Breast Surgery, Wuzhong People's Hospital, 215128, Jiangsu, Suzhou, China.
Enqiao YuDepartment of Breast Surgery, The 1st Affiliated Hospital of Soochow University, Ward 6, 2F Surgical Building, 188 Shizi Street, Gusu District, Jiangsu, 215006, Suzhou, China. enqiao_yu@163.com.
Jianxia LiuDepartment of Breast Surgery, The 1st Affiliated Hospital of Soochow University, Ward 6, 2F Surgical Building, 188 Shizi Street, Gusu District, Jiangsu, 215006, Suzhou, China. jianxia_liu23@sina.com.
Liang SunDepartment of Breast Surgery, The 1st Affiliated Hospital of Soochow University, Ward 6, 2F Surgical Building, 188 Shizi Street, Gusu District, Jiangsu, 215006, Suzhou, China.
Qin HeDepartment of Breast Surgery, The 1st Affiliated Hospital of Soochow University, Ward 6, 2F Surgical Building, 188 Shizi Street, Gusu District, Jiangsu, 215006, Suzhou, China.
Qiran LuDepartment of Breast Surgery, Dushuhu Public Hospital Affiliated to Soochow University, 215006, SuZhou, JiangSu, China.
Soochow University · CNHanzhong People's Hospital · CN

Funding

Young Reserve Talents Development Project of The First Affiliated Hospital of Soochow University Young Reserve Talents Development Project of The First Affiliated Hospital of Soochow University
6 · The paper itself

Abstract

backgroundTriple-negative breast cancer (TNBC) is a special type of breast cancer that lacks effective therapeutic targets. There is a significant need to clarify its pathogenesis, so as to bring new targeted approaches for TNBC management. Here, we identified a long-non coding RNA (lncRNA) ASMTL-AS1 that linked to TNBC development and progression.

methodsQuantitative real-time polymerase chain reaction (qRT-PCR) and Western blot assays were used to test gene and protein levels, respectively. The regulatory axis of miR-1228-3p/SOX17/β-catenin was determined by luciferase reporter and RNA pull-down assays. In vivo assay was conducted by using the nude mice model via subcutaneous transplantation of tumor cells.

resultsASMTL-AS1 was significantly downregulated in TNBC tissues compared to normal tissues, which was closely associated with aggressive clinical features and unfavorable prognosis. Lentivirus-mediated ASMTL-AS1 overexpression evidently reduced the ability of TNBC cell colony formation, activity and invasion by more than 2.5 times. RNA pull-down and luciferase reporter assays revealed that miR-1228-3p directly bound to ASMTL-AS1, ASMTL-AS1 increased SOX17 expression via sponging and repressing miR-1228-3p. Subsequently, the upregulated SOX17 trans-suppressed β-catenin expression, resulting in the inactivation of carcinogenic Wnt/β-catenin signaling, thereby restraining TNBC cell growth and dissemination. Importantly, the xenograft tumor model showed that the ASMTL-AS1 overexpression significantly retarded tumor growth, and negatively regulated Wnt/β-catenin pathway.

conclusionsOur data characterize a novel tumor suppressor in TNBC, restoration of ASMTL-AS1 may be a candidate therapeutic intervention for TNBC patients.

Indexed as

AdultAnimalsbeta CateninCell Line, TumorCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansMiceMice, NudeMicroRNAsNeoplasm InvasivenessRNA, Long NoncodingSOXF Transcription FactorsTriple Negative Breast Neoplasmsbeta CateninCTNNB1 protein, humanMicroRNAsMIRN1228 microRNA, humanRNA, Long NoncodingSOX17 protein, humanSOXF Transcription FactorsASMTL-AS1miRNA spongesPrognosisTNBCWnt/β-catenin pathway

Identifiers

PMID34006305
PMCPMC8130432
OpenAlexW3151629504

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.