Evidence map›Paper›PMID 28031240›Full record

ArticleCancer genomics & proteomics2017

Combination of a STAT3 Inhibitor and an mTOR Inhibitor Against a Temozolomide-resistant Glioblastoma Cell Line.

Haruo Miyata, Tadashi Ashizawa, Akira Iizuka, Ryota Kondou, Chizu Nonomura, Takashi Sugino, Kenichi Urakami, Akira Asai, Nakamasa Hayashi, Koichi Mitsuya and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Cancer genomics & proteomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.1field-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

16 citing papers in PubMed, 40 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

13 authors at 2 institutions in 1 country.

Haruo MiyataImmunotherapy Division, Shizuoka Cancer Center Research Institute, Shizuoka Cancer Center Hospital, Shizuoka, Japan.
Tadashi AshizawaImmunotherapy Division, Shizuoka Cancer Center Research Institute, Shizuoka Cancer Center Hospital, Shizuoka, Japan.
Akira IizukaImmunotherapy Division, Shizuoka Cancer Center Research Institute, Shizuoka Cancer Center Hospital, Shizuoka, Japan.
Ryota KondouImmunotherapy Division, Shizuoka Cancer Center Research Institute, Shizuoka Cancer Center Hospital, Shizuoka, Japan.
Chizu NonomuraImmunotherapy Division, Shizuoka Cancer Center Research Institute, Shizuoka Cancer Center Hospital, Shizuoka, Japan.
Takashi SuginoDivision of Pathology, Shizuoka Cancer Center Hospital, Shizuoka, Japan.
Kenichi UrakamiCancer Diagnostics Division, Shizuoka Cancer Center Research Institute, Shizuoka Cancer Center Hospital, Shizuoka, Japan.
Akira AsaiGraduate School of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Japan.
Nakamasa HayashiDivision of Neurosurgery, Shizuoka Cancer Center Hospital, Shizuoka, Japan.
Koichi MitsuyaDivision of Neurosurgery, Shizuoka Cancer Center Hospital, Shizuoka, Japan.
Yoko NakasuDivision of Neurosurgery, Shizuoka Cancer Center Hospital, Shizuoka, Japan.
Ken YamaguchiOffice of the President, Shizuoka Cancer Center Hospital, Shizuoka, Japan.
Yasuto AkiyamaImmunotherapy Division, Shizuoka Cancer Center Research Institute, Shizuoka Cancer Center Hospital, Shizuoka, Japan y.akiyama@scchr.jp.
Shizuoka Cancer Center · JPUniversity of Shizuoka · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTemozolomide-resistant (TMZ-R) glioblastoma is very difficult to treat, and a novel approach to overcome resistance is needed. MATERIALS AND

methodsThe efficacy of a combination treatment of STAT3 inhibitor, STX-0119, with rapamycin was investigated against our established TMZ-resistant U87 cell line.

resultsThe growth-inhibitory effect of the combination treatment was significant against the TMZ-R U87 cell line (IC

conclusionThese results suggest that the STAT3 pathway is associated with the mTOR downstream pathway mediated by YKL-40 protein, and the combination therapy of the STAT3 inhibitor and rapamycin could be worth developing as a novel therapeutic approach against TMZ-resistant relapsed gliomas.

Indexed as

Drug Resistance, NeoplasmAnimalsAntineoplastic AgentsCell Line, TumorCell ProliferationChitinase-3-Like Protein 1DacarbazineDisease Models, AnimalExomeGlioblastomaHigh-Throughput Nucleotide SequencingHumansMaleOxadiazolesProtein Kinase InhibitorsQuinolinesAntineoplastic AgentsCHI3L1 protein, humanChitinase-3-Like Protein 1DacarbazineOxadiazolesProtein Kinase InhibitorsQuinolinesSTAT3 Transcription FactorSTX-0119TemozolomideTOR Serine-Threonine KinasesglioblastomamTOR inhibitorSTAT3 inhibitortemozolomide resistance

Identifiers

PMID28031240
PMCPMC5267503
OpenAlexW2566211930

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.