Evidence map›Paper›PMID 26848867›Full record

ArticleOncotarget2016

Zoledronate blocks geranylgeranylation not farnesylation to suppress human osteosarcoma U2OS cells metastasis by EMT via Rho A activation and FAK-inhibited JNK and p38 pathways.

Hsin-Lin Cheng, Chiao-Wen Lin, Jia-Sin Yang, Ming-Ju Hsieh, Shun-Fa Yang, Ko-Hsiu Lu

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

32 citing papers in PubMed, 45 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

6 authors at 2 institutions in 1 country.

Hsin-Lin ChengInstitute of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan.
Chiao-Wen LinInstitute of Oral Sciences, Chung Shan Medical University, Taichung 40201, Taiwan.
Jia-Sin YangInstitute of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan.
Ming-Ju HsiehInstitute of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan.
Shun-Fa YangInstitute of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan.
Ko-Hsiu LuDepartment of Orthopedics, Chung Shan Medical University Hospital, Taichung 40201, Taiwan.
Chung Shan Medical University · TWChung Shan Medical University Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Zoledronate is a standard treatment for preventing skeletal complications of osteoporosis and some types of cancer associated with bone metastases, but we little know whether the effect of zoledronate on metastasis of osteosarcoma. Here, we investigated the inhibitory effects of zoledronate on cell viability, motility, migration and invasion of 4 osteosarcoma cell lines (Saos2, MG-63, HOS and U2OS) by affecting cell morphology, epithelial-mesenchymal transition (EMT) and cytoskeletal organization as well as induction of E-cadherin and reduction of N-cadherin with activation of transcription factors Slug and Twist, especially in U2OS cells. Zoledronate decreased JNK and p38 phosphorylation and upper streams of focal adhesion kinase (FAK) and Src to suppress the motility, invasiveness and migration of U2OS cells. In addition to zoledronate-inhibited Rho A and Cdc42 membrane translocation and GTPγS activities, the anti-metastatic effects in U2OS cells including inhibition of adhesion were reversed by geranylgeraniol, but not farnesol. In conclusion, Zoledronate blocks geranylgeranylation not farnesylation to suppress human osteosarcoma U2OS cell-matrix and cell-cell interactions, migration potential, the invasive activity, and the adhesive ability by EMT via Rho A activation and FAK-inhibited JNK and p38 pathways.

Indexed as

Biological TransportBone Density Conservation AgentsBone NeoplasmsCadherinscdc42 GTP-Binding ProteinCell Line, TumorCell MovementCell SurvivalDiphosphonatesDiterpenesEpithelial-Mesenchymal TransitionFarnesolFocal Adhesion Kinase 1Focal Adhesion Protein-Tyrosine KinasesHumansImidazolesBone Density Conservation AgentsCadherinscdc42 GTP-Binding ProteinDiphosphonatesDiterpenesFarnesolFocal Adhesion Kinase 1Focal Adhesion Protein-Tyrosine KinasesgeranylgeraniolImidazolesJNK Mitogen-Activated Protein KinasesNuclear Proteinsp38 Mitogen-Activated Protein KinasesProto-Oncogene Proteins pp60(c-src)PTK2 protein, humanrho-Associated KinasesSNAI1 protein, humanSnail Family Transcription FactorsTWIST1 protein, humanTwist-Related Protein 1Zoledronic AcidgeranylgeranylationmetastasisRho AU2OSzoledronate

Identifiers

PMID26848867
PMCPMC4891081
OpenAlexW2263512295

What OpenQuestion holds

Textmetadata
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.