Evidence map›Paper›PMID 27507059›Full record

ArticleOncotarget2016

Superior efficacy of co-treatment with the dual PI3K/mTOR inhibitor BEZ235 and histone deacetylase inhibitor Trichostatin A against NSCLC.

Junjie Piao, Liyan Chen, Taihao Quan, Longshan Li, Chunji Quan, Yingshi Piao, Tiefeng Jin, Zhenhua Lin

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 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.1field-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

24 citing papers in PubMed, 38 citations in OpenAlex.

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  16. Expression and Comparison of Cbl-b in Lung Squamous Cell Carcinoma and Adenocarcinoma.Medical science monitor : international medical journal of experimental and clinical research · 2018
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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 3 institutions in 2 countries.

Junjie PiaoDepartment of Pathology & Cancer Research Center, Yanbian University Medical College, Yanji 133002, China.
Liyan ChenKey Laboratory of Natural Resources of Changbai Mountain & Functional Molecules (Yanbian University), Ministry of Education, Yanji 133002, China.
Taihao QuanDepartment of Dermatology, University of Michigan Medical School, Michigan 48109-5609, USA.
Longshan LiDepartment of Radiation Oncology, Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, Texas 75390-8807, USA.
Chunji QuanDepartment of Pathology & Cancer Research Center, Yanbian University Medical College, Yanji 133002, China.
Yingshi PiaoDepartment of Pathology & Cancer Research Center, Yanbian University Medical College, Yanji 133002, China.
Tiefeng JinDepartment of Pathology & Cancer Research Center, Yanbian University Medical College, Yanji 133002, China.
Zhenhua LinDepartment of Pathology & Cancer Research Center, Yanbian University Medical College, Yanji 133002, China.
Yanbian University · CNThe University of Texas Southwestern Medical Center · USUniversity of Michigan–Ann Arbor · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-small-cell lung cancer (NSCLC) is the leading cause of cancer-related death worldwide. NSCLC development and progression have recently been correlated with the heightened activation of histone deacetylases (HDACs) and PI3K/Akt signaling pathways. Targeted inhibition of these proteins is promising approach for the development of novel therapeutic strategies to treat patients with advanced NSCLC. For this reason, we combined a dual PI3K and mTOR inhibitor, BEZ235 with the HDAC inhibitor Trichostatin A (TSA), to determine their combined effects on human NSCLC. In this study, we initially discovered that co-treatment with BEZ235 and TSA showed a synergistic effect on inhibition of NSCLC cell proliferation and induction of apoptosis. The combination treatment also synergistically suppressed NSCLC migration, invasion and the NSCLC epithelial-mesenchymal transition (EMT) in vitro. The synergistic effect was also evidenced by declines in xenograft growth and metastasis rates and in ki-67 protein expression in vivo. Together, these results indicated that BEZ235 and TSA combination treatment significantly increased anti-tumor activities compared with BEZ235 and TSA alone, supporting a further evaluation of combination treatment for NSCLC.

Indexed as

Xenograft Model Antitumor AssaysA549 CellsAnimalsAntineoplastic Combined Chemotherapy ProtocolsApoptosisCarcinoma, Non-Small-Cell LungCell Line, TumorCell ProliferationDrug SynergismFemaleHistone Deacetylase InhibitorsHumansHydroxamic AcidsImidazolesLung NeoplasmsMice, Inbred BALB CdactolisibHistone Deacetylase InhibitorsHydroxamic AcidsImidazolesMTOR protein, humanPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsQuinolinesTOR Serine-Threonine Kinasestrichostatin ABEZ235epithelial-mesenchymal transitionnon-small-cell lung cancerTSA

Identifiers

PMID27507059
PMCPMC5312376
OpenAlexW2496640702

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.