Evidence map›Paper›PMID 27206784›Full record

ArticleChinese journal of cancer2016

Hippo/YAP signaling pathway is involved in osteosarcoma chemoresistance.

Dong-Yu Wang, Ya-Nan Wu, Jun-Qi Huang, Wei Wang, Meng Xu, Jin-Peng Jia, Gang Han, Bei-Bei Mao, Wen-Zhi Bi

Abstract read
In one paragraph

Article in Chinese journal of cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
–field-weighted citation impact
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

43 citing papers in PubMed.

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  13. Natural medicinal compounds target signal transduction pathways to overcome ABC drug efflux transporter-mediated multidrug resistance in cancer.Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy · 2023
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  17. Hippo Pathway in Regulating Drug Resistance of Glioblastoma.International journal of molecular sciences · 2021
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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

9 authors.

Dong-Yu WangDepartment of Orthopaedics and Rehabilitation, PLA General Hospital, Fuxing Rd 28, Beijing, 100853, P. R. China.
Ya-Nan WuDepartment of Orthopaedics and Rehabilitation, PLA General Hospital, Fuxing Rd 28, Beijing, 100853, P. R. China.
Jun-Qi HuangDepartment of Orthopaedics and Rehabilitation, PLA General Hospital, Fuxing Rd 28, Beijing, 100853, P. R. China.
Wei WangDepartment of Orthopaedics and Rehabilitation, PLA General Hospital, Fuxing Rd 28, Beijing, 100853, P. R. China.
Meng XuDepartment of Orthopaedics and Rehabilitation, PLA General Hospital, Fuxing Rd 28, Beijing, 100853, P. R. China.
Jin-Peng JiaDepartment of Orthopaedics and Rehabilitation, PLA General Hospital, Fuxing Rd 28, Beijing, 100853, P. R. China.
Gang HanDepartment of Orthopaedics and Rehabilitation, PLA General Hospital, Fuxing Rd 28, Beijing, 100853, P. R. China.
Bei-Bei MaoState Key Laboratory of Brain and Cognitive Sciences, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, P. R. China.
Wen-Zhi BiDepartment of Orthopaedics and Rehabilitation, PLA General Hospital, Fuxing Rd 28, Beijing, 100853, P. R. China. biwenzhi@sina.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsteosarcoma is the most common bone malignancy in children and adolescents, and 20%-30% of the patients suffer from poor prognosis because of individual chemoresistance. The Hippo/yes-associated protein (YAP) signaling pathway has been shown to play a role in tumor chemoresistance, but no previous report has focused on its involvement in osteosarcoma chemoresistance. This study aimed to investigate the role of the Hippo/YAP signaling pathway in osteosarcoma chemoresistance and to determine potential treatment targets.

methodsUsing the Cell Titer-Glo Luminescent cell viability assay and flow cytometry analysis, we determined the proliferation and chemosensitivity of YAP-overexpressing and YAP-knockdown osteosarcoma cells. In addition, using western blotting and the real-time polymerase chain reaction technique, we investigated the alteration of the Hippo/YAP signaling pathway in osteosarcoma cells treated with chemotherapeutic agents.

resultsMammalian sterile 20-like kinase 1 (MST1) degradation was increased, and large tumor suppressor kinase 1/2 (LATS1/2) total protein levels were decreased by methotrexate and doxorubicin, which increased activation and nuclear translocation of YAP. Moreover, YAP increased the proliferation and chemoresistance of MG63 cells.

conclusionsThe Hippo/YAP signaling pathway plays a role in osteosarcoma chemoresistance, and YAP is a potential target for reducing chemoresistance.

Indexed as

Drug Resistance, NeoplasmAdaptor Proteins, Signal TransducingAntineoplastic AgentsBone NeoplasmsCell Line, TumorCell ProliferationCell SurvivalDoxorubicinGene Expression Regulation, NeoplasticHippo Signaling PathwayHumansMethotrexateOsteosarcomaPhosphoproteinsProtein Serine-Threonine KinasesSignal TransductionAdaptor Proteins, Signal TransducingAntineoplastic AgentsDoxorubicinMethotrexatePhosphoproteinsProtein Serine-Threonine KinasesTranscription FactorsYAP1 protein, humanYAP-Signaling ProteinsChemoresistanceDoxorubicinHippoMethotrexateOsteosarcomaYAP

Identifiers

PMID27206784
PMCPMC4875723

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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.