Evidence map›Paper›PMID 31138318›Full record

ArticleJournal of experimental & clinical cancer research : CR2019

The TGFβ-miR-499a-SHKBP1 pathway induces resistance to EGFR inhibitors in osteosarcoma cancer stem cell-like cells.

Tian Wang, Dexing Wang, Lian Zhang, Ping Yang, Jing Wang, Qi Liu, Fei Yan, Feng Lin

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 3% 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, 1 synthesis or guideline pooled it, 50 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

8 authors at 1 institution in 1 country.

Tian WangDepartment of Oncology, The Eighth People's Hospital of Shanghai, No. 8 Caobao Road, Xuhui District, Shanghai, 200233, People's Republic of China.
Dexing WangDepartment of Oncology, The Eighth People's Hospital of Shanghai, No. 8 Caobao Road, Xuhui District, Shanghai, 200233, People's Republic of China.
Lian ZhangDepartment of Oncology, The Eighth People's Hospital of Shanghai, No. 8 Caobao Road, Xuhui District, Shanghai, 200233, People's Republic of China.
Ping YangDepartment of Oncology, The Eighth People's Hospital of Shanghai, No. 8 Caobao Road, Xuhui District, Shanghai, 200233, People's Republic of China.
Jing WangDepartment of Oncology, The Eighth People's Hospital of Shanghai, No. 8 Caobao Road, Xuhui District, Shanghai, 200233, People's Republic of China.
Qi LiuDepartment of Oncology, The Eighth People's Hospital of Shanghai, No. 8 Caobao Road, Xuhui District, Shanghai, 200233, People's Republic of China.
Fei YanDepartment of Oncology, The Eighth People's Hospital of Shanghai, No. 8 Caobao Road, Xuhui District, Shanghai, 200233, People's Republic of China.
Feng LinDepartment of Oncology, The Eighth People's Hospital of Shanghai, No. 8 Caobao Road, Xuhui District, Shanghai, 200233, People's Republic of China. linfengdoc@163.com.ORCID http://orcid.org/0000-0003-3826-0687
Shanghai Eighth People Hospital · CN

Funding

Medical Peak Discipline Construction Project of Xuhui District 15303Medical Science and Technology Project of Xuhui District SHXH201709
6 · The paper itself

Abstract

BACKGROUND/

aimsA novel paradigm in tumor biology suggests that osteosarcoma (OS) chemo-resistance is driven by osteosarcoma stem cell-like cells (OSCs). As the sensitivity of only a few tumors to epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) can be explained by the presence of EGFR tyrosine kinase (TK) domain mutations, there is a need to elucidate mechanisms of resistance to EGFR-targeted therapies in OS that do not harbor TK sensitizing mutations to develop new strategies to circumvent resistance to EGFR inhibitors.

methodsAs a measure of the characters of OSCs, serum-free cultivation, cell viability test with erlotinib, and serial transplantation in vivo was used. Western blot assays were used to detect the association between erlotinib resistance and transforming growth factor beta (TGFβ)-induced epithelial-to-mesenchymal transition (EMT) progression. By using TaqMan qPCR miRNA array, online prediction software, luciferase reporter assays and western blot analysis, we further elucidated the mechanisms.

resultsHere, CD166

conclusionTGFβ-miR-499a-SHKBP1 network orchestrates the EMT-associated kinase switch that induces resistance to EGFR inhibitors in CD166

Indexed as

Drug Resistance, NeoplasmAnimalsBone NeoplasmsCell Culture TechniquesCell Line, TumorCulture Media, Serum-FreeEpithelial-Mesenchymal TransitionErbB ReceptorsErlotinib HydrochlorideFemaleHumansIntracellular Signaling Peptides and ProteinsMiceMicroRNAsNeoplasm TransplantationNeoplastic Stem CellsCulture Media, Serum-FreeEGFR protein, humanErbB ReceptorsErlotinib HydrochlorideIntracellular Signaling Peptides and ProteinsMicroRNAsMIRN499 microRNA, humanProtein Kinase InhibitorsSETA binding protein 1, humanTransforming Growth Factor betaEGFREpithelial-to-mesenchymal transitionmiR-499aOsteosarcoma stem cell-like cellsSHKBP1TGFβ

Identifiers

PMID31138318
PMCPMC6540516
OpenAlexW2947803991

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.