Evidence map›Paper›PMID 29706651›Full record

ArticleOncogene2018

Wild-type p53 upregulates an early onset breast cancer-associated gene GAS7 to suppress metastasis via GAS7-CYFIP1-mediated signaling pathway.

Jer-Wei Chang, Wen-Hung Kuo, Chiao-Mei Lin, Wen-Ling Chen, Shih-Hsuan Chan, Meng-Fan Chiu, I-Shou Chang, Shih-Sheng Jiang, Fang-Yu Tsai, Chung-Hsing Chen and 12 more

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
44.3field-weighted citation impact, top 1% 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

33 citing papers in PubMed, 537 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

22 authors at 10 institutions in 1 country.

Jer-Wei ChangInstitute of Molecular and Genomic Medicine, National Health Research Institute, Miaoli, Taiwan.
Wen-Hung KuoDepartment of Surgery, National Taiwan University Hospital, Taipei, Taiwan.
Chiao-Mei LinInstitute of Molecular and Genomic Medicine, National Health Research Institute, Miaoli, Taiwan.
Wen-Ling ChenInstitute of Molecular and Genomic Medicine, National Health Research Institute, Miaoli, Taiwan.
Shih-Hsuan ChanInstitute of Molecular and Genomic Medicine, National Health Research Institute, Miaoli, Taiwan.
Meng-Fan ChiuInstitute of Molecular and Genomic Medicine, National Health Research Institute, Miaoli, Taiwan.
I-Shou ChangNational Institute of Cancer Research, National Health Research Institutes, Miaoli, Taiwan.
Shih-Sheng JiangNational Institute of Cancer Research, National Health Research Institutes, Miaoli, Taiwan.ORCID http://orcid.org/0000-0003-1909-437X
Fang-Yu TsaiNational Institute of Cancer Research, National Health Research Institutes, Miaoli, Taiwan.
Chung-Hsing ChenNational Institute of Cancer Research, National Health Research Institutes, Miaoli, Taiwan.
Pei-Hsin HuangDepartment of Pathology, College of Medicine, National Taiwan University, Taipei, Taiwan.
King-Jen ChangDepartment of Surgery, National Taiwan University Hospital, Taipei, Taiwan.
Kai-Ti LinInstitute of Biotechnology, College of Life Science, National Tsing Hua University, Hsinchu, Taiwan.
Sheng-Chieh LinCollege of Chinese Medicine, China Medical University, Taichung, Taiwan.
Ming-Yang WangDepartment of Surgery, National Taiwan University Hospital, Taipei, Taiwan.
Yih-Huei UenDepartment of Surgery, Asia University Hospital, Taichung, Taiwan.
Chi-Wen TuDepartment of General Surgery, Ditmanson Medical Foundation Chia-Yi Christian Hospital, Chiayi, Taiwan.
Ming-Feng HouDepartment of Surgery, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
Shih-Feng TsaiInstitute of Molecular and Genomic Medicine, National Health Research Institute, Miaoli, Taiwan.
Chen-Yang ShenInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Shiao-Lin TungDepartment of Hematology and Oncology, Ton-Yen General Hospital, Hsinchu, Taiwan.
Lu-Hai WangInstitute of Molecular and Genomic Medicine, National Health Research Institute, Miaoli, Taiwan. luhaiwang@mail.cmu.edu.tw.
National Health Research Institutes · TWNational Taiwan University Hospital · TWAsia University · TWChia-Yi Christian Hospital · TWChina Medical University · TWInstitute of Biomedical Sciences, Academia Sinica · TWKaohsiung Medical University · TWNational Taiwan University · TWNational Tsing Hua University · TWTaiwan Adventist Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The early onset breast cancer patients (age ≤ 40) often display higher incidence of axillary lymph node metastasis, and poorer five-year survival than the late-onset patients. To identify the genes and molecules associated with poor prognosis of early onset breast cancer, we examined gene expression profiles from paired breast normal/tumor tissues, and coupled with Gene Ontology and public data base analysis. Our data showed that the expression of GAS7b gene was lower in the early onset breast cancer patients as compared to the elder patients. We found that GAS7 was associated with CYFIP1 and WAVE2 complex to suppress breast cancer metastasis via blocking CYFIP1 and Rac1 protein interaction, actin polymerization, and β1-integrin/FAK/Src signaling. We further demonstrated that p53 directly regulated GAS7 gene expression, which was inversely correlated with p53 mutations in breast cancer specimens. Our study uncover a novel regulatory mechanism of p53 in early onset breast cancer progression through GAS7-CYFIP1-mediated signaling pathways.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsBreast NeoplasmsCell Line, TumorFemaleFocal Adhesion Kinase 1Gene Expression Regulation, NeoplasticHumansIntegrin beta1Lymphatic MetastasisMCF-7 CellsMiceNerve Tissue ProteinsProto-Oncogene Proteins pp60(c-src)Signal TransductionTumor Suppressor Protein p53Adaptor Proteins, Signal TransducingCYFIP1 protein, humanFocal Adhesion Kinase 1GAS7 protein, humanIntegrin beta1Nerve Tissue ProteinsProto-Oncogene Proteins pp60(c-src)TP53 protein, humanTumor Suppressor Protein p53Wiskott-Aldrich Syndrome Protein Family

Identifiers

PMID29706651
PMCPMC6062498
OpenAlexW2801606086

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.