Evidence map›Paper›PMID 33536579›Full record

ArticleOncogene2021

MiR-211 determines brain metastasis specificity through SOX11/NGN2 axis in triple-negative breast cancer.

Jhih-Kai Pan, Cheng-Han Lin, Yao-Lung Kuo, Luo-Ping Ger, Hui-Chuan Cheng, Yun-Chin Yao, Michael Hsiao, Pei-Jung Lu

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 10% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

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  17. miR-216b-5p promotes late apoptosis/necroptosis in trastuzumab-resistant SK-BR-3 cells.Turkish journal of biology = Turk biyoloji dergisi · 2023
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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

8 authors at 4 institutions in 1 country.

Jhih-Kai Pan *Institute of Clinical Medicine, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Cheng-Han Lin *Institute of Clinical Medicine, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Yao-Lung KuoDepartment of General Surgery, National Cheng Kung University Hospital, Tainan, Taiwan.
Luo-Ping GerDepartment of Medical Education and Research, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan.
Hui-Chuan ChengInstitute of Clinical Medicine, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Yun-Chin YaoClinical Medicine Research Center, National Cheng Kung University Hospital, Tainan, Taiwan.
Michael HsiaoGenomics Research Center, Academia Sinica, Taipei, Taiwan.ORCID http://orcid.org/0000-0001-8529-9213
Pei-Jung LuInstitute of Clinical Medicine, College of Medicine, National Cheng Kung University, Tainan, Taiwan. pjlu2190@mail.ncku.edu.tw.ORCID http://orcid.org/0000-0002-8143-5668
National Cheng Kung University · TWNational Cheng Kung University Hospital · TWKaohsiung Medical University · TWKaohsiung Veterans General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brian metastasis, which is diagnosed in 30% of triple-negative breast cancer (TNBC) patients with metastasis, causes poor survival outcomes. Growing evidence has characterized miRNAs involving in breast cancer brain metastasis; however, currently, there is a lack of prognostic plasma-based indicator for brain metastasis. In this study, high level of miR-211 can act as brain metastatic prognostic marker in vivo. High miR-211 drives early and specific brain colonization through enhancing trans-blood-brain barrier (BBB) migration, BBB adherence, and stemness properties of tumor cells and causes poor survival in vivo. SOX11 and NGN2 are the downstream targets of miR-211 and negatively regulate miR-211-mediated TNBC brain metastasis in vitro and in vivo. Most importantly, high miR-211 is correlated with poor survival and brain metastasis in TNBC patients. Our findings suggest that miR-211 may be used as an indicator for TNBC brain metastasis.

Indexed as

Basic Helix-Loop-Helix ProteinsBrain NeoplasmsCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansMicroRNAsNeoplasm InvasivenessNeoplasm MetastasisNerve Tissue ProteinsSOXC Transcription FactorsTriple Negative Breast NeoplasmsBasic Helix-Loop-Helix ProteinsMicroRNAsMIRN211 microRNA, humanNerve Tissue ProteinsNEUROG2 protein, humanSOX11 protein, humanSOXC Transcription Factors

Identifiers

PMID33536579
PMCPMC7932919
OpenAlexW3129087799

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.