Evidence map›Paper›PMID 28042875›Full record

ArticleActa pharmacologica Sinica2017

The PI3K/mTOR dual inhibitor BEZ235 suppresses proliferation and migration and reverses multidrug resistance in acute myeloid leukemia.

Lan Deng, Ling Jiang, Xiang-Hua Lin, Kuo-Fu Tseng, Yuan Liu, Xing Zhang, Rui-Hong Dong, Zhi-Gang Lu, Xiu-Ju Wang

Open access · bronzeAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

35 citing papers in PubMed, 55 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

9 authors at 4 institutions in 2 countries.

Lan DengDepartment of Hematology/Key Laboratory of Malignant Tumor Gene Regulation and Target Therapy of Guangdong Higher Education Institutes, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou 510120, China.
Ling JiangDepartment of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Xiang-Hua LinDepartment of Hematology/Key Laboratory of Malignant Tumor Gene Regulation and Target Therapy of Guangdong Higher Education Institutes, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou 510120, China.
Kuo-Fu TsengBiophysics Department of Oregon State University, ALS-2139 Corvallis, OR 97330, USA.
Yuan LiuDepartment of Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou 501282, China.
Xing ZhangDepartment of Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou 501282, China.
Rui-Hong DongDepartment of Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou 501282, China.
Zhi-Gang LuDepartment of Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou 501282, China.
Xiu-Ju WangDepartment of Hematology/Key Laboratory of Malignant Tumor Gene Regulation and Target Therapy of Guangdong Higher Education Institutes, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou 510120, China.
Southern Medical University · CNSun Yat-sen Memorial Hospital · CNOregon State University · USSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aberrant activation of the PI3K/Akt/mTOR pathway contributes to the proliferation of malignant cells, and may confer resistance to chemotherapy in various malignancies, including acute myeloid leukemia (AML). Chemoresistance is the major reason for relapse in AML. RAD001 (everolimus) has been used at d1 and d7 of an induction chemotherapy regimen for AML, which has acceptable toxicity and may improve conventional chemotherapeutic treatment. Dual inhibitors of PI3K and mTOR overcome some of the intrinsic disadvantages of rapamycin and its derivatives. In this study, we evaluated the effects of BEZ235, a PI3K/mTOR dual inhibitor, on the multidrug-resistant AML cell lines HL-60/VCR and K562/ADR in vitro. BEZ235 dose-dependently inhibited the viability of HL-60/VCR and K562/ADR cells with the IC

Indexed as

Phosphoinositide-3 Kinase InhibitorsAdaptor Proteins, Signal TransducingAntineoplastic AgentsATP Binding Cassette Transporter, Subfamily BCell Line, TumorCell MovementCell ProliferationDrug Resistance, MultipleDrug Resistance, NeoplasmEndothelin-1HumansImidazolesLeukemia, Myeloid, AcuteMicroRNAsProtein Kinase InhibitorsQuinolinesABCB1 protein, humanAdaptor Proteins, Signal TransducingAntineoplastic AgentsATP Binding Cassette Transporter, Subfamily BBAG4 protein, humandactolisibEndothelin-1ImidazolesMicroRNAsMIRN1 microRNA, humanMTOR protein, humanPhosphoinositide-3 Kinase InhibitorsProtein Kinase InhibitorsQuinolinesTOR Serine-Threonine Kinases

Identifiers

PMID28042875
PMCPMC5342661
OpenAlexW2562206761

What OpenQuestion holds

Textmetadata
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.