Evidence map›Paper›PMID 28960945›Full record

ArticleCancer medicine2017

Novel ATP-competitive Akt inhibitor afuresertib suppresses the proliferation of malignant pleural mesothelioma cells.

Masayuki Yamaji, Akinobu Ota, Md Wahiduzzaman, Sivasundaram Karnan, Toshinori Hyodo, Hiroyuki Konishi, Shinobu Tsuzuki, Yoshitaka Hosokawa, Masayuki Haniuda

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2017. 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
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

32 citing papers in PubMed, 56 citations in OpenAlex.

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  13. Neutrophil Survival Signaling DuringFrontiers in cellular and infection microbiology · 2022
    Article
  14. Article
  15. ACTL6A suppresses p21Oncogenesis · 2021
    Article
  16. Article
  17. Review
  18. Article
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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 1 institution in 1 country.

Masayuki YamajiDivision of Chest Surgery, Department of Surgery, Aichi Medical University School of Medicine, Nagakute, Aichi, 480-1195, Japan.
Akinobu OtaDepartment of Biochemistry, Aichi Medical University School of Medicine, Nagakute, Aichi, 480-1195, Japan.ORCID http://orcid.org/0000-0002-6296-2921
Md WahiduzzamanDepartment of Biochemistry, Aichi Medical University School of Medicine, Nagakute, Aichi, 480-1195, Japan.
Sivasundaram KarnanDepartment of Biochemistry, Aichi Medical University School of Medicine, Nagakute, Aichi, 480-1195, Japan.
Toshinori HyodoDepartment of Biochemistry, Aichi Medical University School of Medicine, Nagakute, Aichi, 480-1195, Japan.
Hiroyuki KonishiDepartment of Biochemistry, Aichi Medical University School of Medicine, Nagakute, Aichi, 480-1195, Japan.
Shinobu TsuzukiDepartment of Biochemistry, Aichi Medical University School of Medicine, Nagakute, Aichi, 480-1195, Japan.
Yoshitaka HosokawaDepartment of Biochemistry, Aichi Medical University School of Medicine, Nagakute, Aichi, 480-1195, Japan.
Masayuki HaniudaDivision of Chest Surgery, Department of Surgery, Aichi Medical University School of Medicine, Nagakute, Aichi, 480-1195, Japan.
Aichi Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignant pleural mesothelioma (MPM), an asbestos-related occupational disease, is an aggressive and incurable tumor of the thoracic cavity. Despite recent advances in MPM treatment, overall survival of patients with MPM is very low. Recent studies have implicated that PI3K/Akt signaling is involved in MPM cell survival and development. To investigate the effects of Akt inhibitors on MPM cell survival, we examined the effects of nine selective Akt inhibitors, namely, afuresertib, Akti-1/2, AZD5363, GSK690693, ipatasertib, MK-2206, perifosine, PHT-427, and TIC10, on six MPM cell lines, namely, ACC-MESO-4, Y-MESO-8A, MSTO-211H, NCI-H28, NCI-H290, and NCI-H2052, and a normal mesothelial cell line MeT-5A. Comparison of IC

Indexed as

Antineoplastic AgentsApoptosisBenzenesulfonamidesBenzylaminesCaspase 3Caspase 7Cell Line, TumorCyclin-Dependent Kinase Inhibitor p21Forkhead Box Protein O1G1 Phase Cell Cycle CheckpointsGene Expression Regulation, NeoplasticGlycogen Synthase Kinase 3 betaHeterocyclic Compounds, 3-RingHeterocyclic Compounds, 4 or More RingsHumansImidazoles4-dodecyl-N-(1,3,4-thiadiazol-2-yl)benzenesulfonamideafuresertibAkt-I-1,2 compoundAntineoplastic AgentsBenzenesulfonamidesBenzylaminescapivasertibCaspase 3Caspase 7CDKN1A protein, humanCyclin-Dependent Kinase Inhibitor p21Forkhead Box Protein O1Glycogen Synthase Kinase 3 betaGSK690693Heterocyclic Compounds, 3-RingHeterocyclic Compounds, 4 or More RingsImidazolesMK 2206OxadiazolesperifosinePhosphorylcholineProtein Kinase InhibitorsProto-Oncogene Proteins c-aktPyrazolesPyridinesPyrimidinesPyrrolesQuinoxalinesSulfonamidesThiadiazolesThiophenesTIC10 compoundAfuresertibAkt inhibitorcancer therapyMesothelioma

Identifiers

PMID28960945
PMCPMC5673922
OpenAlexW2756610635

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.