Evidence map›Paper›PMID 35285795›Full record

ArticleeLife2022

Binding blockade between TLN1 and integrin β1 represses triple-negative breast cancer.

Yixiao Zhang, Lisha Sun, Haonan Li, Liping Ai, Qingtian Ma, Xinbo Qiao, Jie Yang, Hao Zhang, Xunyan Ou, Yining Wang and 6 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 22 citations in OpenAlex.

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  11. The ancestral type of the R-RAS protein has oncogenic potential.Cellular & molecular biology letters · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 3 institutions in 2 countries.

Yixiao Zhang *Department of Oncology, Shengjing Hospital of China Medical University, Shenyang, China.
Lisha Sun *Department of Oncology, Shengjing Hospital of China Medical University, Shenyang, China.ORCID https://orcid.org/0000-0002-4095-5026
Haonan Li *School of Bioengineering, Dalian University of Technology, Dalian, China.
Liping AiCancer Stem Cell and Translational Medicine Laboratory, Shengjing Hospital of China Medical University, Shenyang, China.
Qingtian MaDepartment of Oncology, Shengjing Hospital of China Medical University, Shenyang, China.
Xinbo QiaoDepartment of Oncology, Shengjing Hospital of China Medical University, Shenyang, China.ORCID https://orcid.org/0000-0002-6759-921X
Jie YangCancer Stem Cell and Translational Medicine Laboratory, Shengjing Hospital of China Medical University, Shenyang, China.
Hao ZhangCancer Stem Cell and Translational Medicine Laboratory, Shengjing Hospital of China Medical University, Shenyang, China.
Xunyan OuCancer Stem Cell and Translational Medicine Laboratory, Shengjing Hospital of China Medical University, Shenyang, China.
Yining WangCancer Stem Cell and Translational Medicine Laboratory, Shengjing Hospital of China Medical University, Shenyang, China.
Guanglei ChenDepartment of Oncology, Shengjing Hospital of China Medical University, Shenyang, China.
Jinqi XueDepartment of Oncology, Shengjing Hospital of China Medical University, Shenyang, China.
Xudong ZhuDepartment of Oncology, Shengjing Hospital of China Medical University, Shenyang, China.
Yu ZhaoDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, United States.
Yongliang YangDepartment of Oncology, Shengjing Hospital of China Medical University, Shenyang, China.
Caigang LiuDepartment of Oncology, Shengjing Hospital of China Medical University, Shenyang, China.ORCID https://orcid.org/0000-0003-3729-2839
China Medical University · CNDalian University of Technology · CNWinnMed · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Integrin family are known as key gears in focal adhesion for triple-negative breast cancer (TNBC) metastasis. However, the integrin independent factor TLN1 remains vague in TNBC. Methods: Bioinformatics analysis was performed based on TCGA database and Shengjing Hospital cohort. Western blot and RT-PCR were used to detect the expression of TLN1 and integrin pathway in cells. A small-molecule C67399 was screened for blocking TLN1 and integrin β1 through a novel computational screening approach by targeting the protein-protein binding interface. Drug pharmacodynamics were determined through xenograft assay. Results: Upregulation of TLN1 in TNBC samples correlates with metastasis and worse prognosis. Silencing Conclusions: TLN1 overexpression contributes to TNBC metastasis and C67399 targeting TLN1 may hold promise for TNBC treatment. Funding: This study was supported by grants from the National Natural Science Foundation of China (No. 81872159, 81902607, 81874301), Liaoning Colleges Innovative Talent Support Program (Name: Cancer Stem Cell Origin and Biological Behaviour), Outstanding Scientific Fund of Shengjing Hospital (201803), and Outstanding Young Scholars of Liaoning Province (2019-YQ-10).

Indexed as

Triple Negative Breast NeoplasmsCell Line, TumorCell MovementCell ProliferationFocal AdhesionsHumansIntegrin beta1IntegrinsTalinIntegrin beta1IntegrinsTalinTLN1 protein, humancell adhesionhumanmedicinemousesmall moleculeTLN1triple-negative breast cancer

Identifiers

PMID35285795
PMCPMC8937232
OpenAlexW4221001947

What OpenQuestion holds

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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.