Evidence map›Paper›PMID 31713604›Full record

ArticleCarcinogenesis2020

Transactivation of SOX5 by Brachyury promotes breast cancer bone metastasis.

Ming Chen, Shitao Zou, Chao He, Jundong Zhou, Suoyuan Li, Minghong Shen, Rulei Cheng, Donglai Wang, Tianming Zou, Xueqi Yan and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Carcinogenesis, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 25 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

12 authors at 2 institutions in 1 country.

Ming ChenDepartment of Orthopeadic Surgery, Suzhou, Jiangsu, People's Republic of China.
Shitao ZouSuzhou Cancer Center Core Laboratory, Suzhou, Jiangsu, People's Republic of China.
Chao HeSuzhou Cancer Center Core Laboratory, Suzhou, Jiangsu, People's Republic of China.
Jundong ZhouSuzhou Cancer Center Core Laboratory, Suzhou, Jiangsu, People's Republic of China.
Suoyuan LiDepartment of Orthopeadic Surgery, Suzhou, Jiangsu, People's Republic of China.
Minghong ShenDepartment of Pathology, the Affiliated Suzhou Hospital of Nanjing Medical University; Suzhou Municipal Hospital, Suzhou, Jiangsu, People's Republic of China.
Rulei ChengDepartment of Pathology, the Affiliated Suzhou Hospital of Nanjing Medical University; Suzhou Municipal Hospital, Suzhou, Jiangsu, People's Republic of China.
Donglai WangDepartment of Orthopeadic Surgery, Suzhou, Jiangsu, People's Republic of China.
Tianming ZouDepartment of Orthopeadic Surgery, Suzhou, Jiangsu, People's Republic of China.
Xueqi YanSuzhou Cancer Center Core Laboratory, Suzhou, Jiangsu, People's Republic of China.
Ying HuangDepartment of Ultrasonography, the Fifth People's Hospital of Suzhou, Suzhou, Jiangsu, People's Republic of China.
Jun ShenDepartment of Orthopeadic Surgery, Suzhou, Jiangsu, People's Republic of China.
The Fifth People’s Hospital of Suzhou · CNNanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The bone marrow has been long known to host a unique environment amenable to colonization by metastasizing tumor cells. Yet, the underlying molecular interactions which give rise to the high incidence of bone metastasis (BM) in breast cancer patients have long remained uncharacterized. In our study, in vitro and in vivo assays demonstrated that Brachyury (Bry) could promote breast cancer BM. Bry drives epithelial-mesenchymal transition (EMT) and promotes breast cancer aggressiveness. As an EMT driver, SOX5 involves in breast cancer metastasis and the specific function in BM. Chromatin immunoprecipitation (ChIP) assays revealed SOX5 is a direct downstream target gene of Bry. ChIP analysis and reporter assays identified two Bry-binding motifs; one consistent with the classic conserved binding sequence and the other a new motif sequence. This study demonstrates for the first time that Bry promotes breast cancer cells BM through activating SOX5. In clinical practice, targeting the Bry-Sox5-EMT pathway is evolving into a promising avenue for the prevention of bone metastatic relapse, therapeutic resistance and other aspects of breast cancer progression. Brachyury directly regulates the expression of SOX5 by binding to two motifs in its promoter region. The Bry-SOX5-EMT pathway may represent a potential target to develop treatments to prevent and treat bone metastasis from breast cancer.

Indexed as

Gene Expression Regulation, NeoplasticTranscriptional ActivationAnimalsApoptosisBiomarkers, TumorBone NeoplasmsBrachyury ProteinBreast NeoplasmsCell AdhesionCell MovementCell ProliferationDisease ProgressionEpithelial-Mesenchymal TransitionFemaleFetal ProteinsHumansBiomarkers, TumorBrachyury ProteinFetal ProteinsSOX5 protein, humanSOXD Transcription FactorsT-Box Domain Proteins

Identifiers

PMID31713604
PMCPMC7350557
OpenAlexW2984594504

What OpenQuestion holds

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LicenceCC BY-NC
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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.