Evidence map›Paper›PMID 26462147›Full record

ArticleOncotarget2015

GIT1 promotes lung cancer cell metastasis through modulating Rac1/Cdc42 activity and is associated with poor prognosis.

Jeng-Shou Chang, Chia-Yi Su, Wen-Hsuan Yu, Wei-Jiunn Lee, Yu-Peng Liu, Tsung-Ching Lai, Yi-Hua Jan, Yi-Fang Yang, Chia-Ning Shen, Jin-Yuh Shew and 8 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 48 citations in OpenAlex.

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  14. Arf GAPs as Regulators of the Actin Cytoskeleton-An Update.International journal of molecular sciences · 2019
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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

18 authors at 9 institutions in 2 countries.

Jeng-Shou ChangInstitute of Biochemistry and Molecular Biology, National Yang-Ming University, Taipei, Taiwan.
Chia-Yi SuMedical Biology, Genomics Research Center, Academia Sinica, Taipei, Taiwan.
Wen-Hsuan YuDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Wei-Jiunn LeeDepartment of Urology, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Yu-Peng LiuInstitute of Genomic Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
Tsung-Ching LaiMedical Biology, Genomics Research Center, Academia Sinica, Taipei, Taiwan.
Yi-Hua JanMedical Biology, Genomics Research Center, Academia Sinica, Taipei, Taiwan.
Yi-Fang YangMedical Biology, Genomics Research Center, Academia Sinica, Taipei, Taiwan.
Chia-Ning ShenMedical Biology, Genomics Research Center, Academia Sinica, Taipei, Taiwan.
Jin-Yuh ShewMedical Biology, Genomics Research Center, Academia Sinica, Taipei, Taiwan.
Jean LuMedical Biology, Genomics Research Center, Academia Sinica, Taipei, Taiwan.
Chih-Jen YangDepartment of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.
Ming-Shyan HuangDepartment of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.
Pei-Jung LuInstitute of Clinical Medicine, Medical College, National Cheng Kung University, Tainan, Taiwan.
Yuan-Feng LinGraduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Min-Liang KuoInstitute of Biochemical Science, National Taiwan University College of Life Science, Taipei, Taiwan.
Kuo-Tai HuaGraduate Institute of Toxicology, National Taiwan University College of Medicine, Taipei, Taiwan.
Michael HsiaoMedical Biology, Genomics Research Center, Academia Sinica, Taipei, Taiwan.
Genomics Research Center, Academia Sinica · TWKaohsiung Medical University · TWNational Taiwan University · TWKaohsiung Medical University Chung-Ho Memorial Hospital · TWNational Cheng Kung University · TWNational Yang Ming Chiao Tung University · TWTaipei Medical University · TWThe University of Texas MD Anderson Cancer Center · USWan Fang Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

G-protein-coupled receptor kinase interacting protein 1 (GIT1) is participated in cell movement activation, which is a fundamental process during tissue development and cancer progression. GIT1/PIX forming a functional protein complex that contributes to Rac1/Cdc42 activation, resulting in increasing cell mobility. Although the importance of Rac1/Cdc42 activation is well documented in cancer aggressiveness, the clinical importance of GIT1 remains largely unknown. Here, we investigated the clinical significance of GIT1 expression in non-small-cell lung cancer (NSCLC) and also verified the importance of GIT1-Rac1/Cdc42 axis in stimulating NSCLC cell mobility. The result indicated higher GIT1 expression patients had significantly poorer prognoses in disease-free survival (DFS) and overall survival (OS) compared with lower GIT1 expression patients. Higher GIT1 expression was an independent prognostic factor by multivariate analysis and associated with migration/invasion of NSCLC cells in transwell assay. In vivo studies indicated that GIT1 promotes metastasis of NSCLC cells. Finally, GIT1 was found to stimulate migration/invasion by altering the activity of Rac1/Cdc42 in NSCLC cells. Together, the GIT1 expression is associated with poor prognosis in patients with NSCLC. GIT1 is critical for the invasiveness of NSCLC cells through stimulating the activity of Rac1/Cdc42.

Indexed as

Adaptor Proteins, Signal TransducingAgedCarcinoma, Non-Small-Cell Lungcdc42 GTP-Binding ProteinCell Cycle ProteinsCell Line, TumorFemaleHumansLung NeoplasmsMaleMiddle AgedNeoplasm MetastasisPrognosisrac1 GTP-Binding ProteinSignal TransductionTransfectionAdaptor Proteins, Signal Transducingcdc42 GTP-Binding ProteinCell Cycle ProteinsGIT1 protein, humanrac1 GTP-Binding ProteinRAC1 protein, humanGIT1lung cancer prognosismetastasisRac1/Cdc42Rho GTPases

Identifiers

PMID26462147
PMCPMC4742177
OpenAlexW2275812893

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.