Evidence map›Paper›PMID 28418085›Full record

ArticleCancer science2017

Puquitinib, a novel orally available PI3Kδ inhibitor, exhibits potent antitumor efficacy against acute myeloid leukemia.

Chengying Xie, Ye He, Mingyue Zhen, Yulan Wang, Yongping Xu, Liguang Lou

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed, 27 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

6 authors at 1 institution in 1 country.

Chengying XieShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
Ye HeShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
Mingyue ZhenShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
Yulan WangShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
Yongping XuShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
Liguang LouShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.ORCID http://orcid.org/0000-0001-7396-7122
Chinese Academy of Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The PI3Kδ isoform (PIK3CD), also known as P110δ, is predominately expressed in leukocytes and has been implicated as a potential target in the treatment of hematological malignancies. In this report, we detailed the pharmacologic properties of puquitinib, a novel, orally available PI3Kδ inhibitor. Puquitinib, which binds to the ATP-binding pocket of PI3Kδ, was highly selective and potent for PI3Kδ relative to other PI3K isoforms and a panel of protein kinases, exhibiting low-nanomolar biochemical and cellular inhibitory potencies. Additional cellular profiling demonstrated that puquitinib inhibited proliferation, induced G

Indexed as

Leukemia, Myeloid, AcuteAdenineAminoquinolinesAnimalsAntineoplastic AgentsBlotting, WesternCell ProliferationClass I Phosphatidylinositol 3-KinasesHumansMiceMice, Inbred BALB CMice, NudeMolecular Docking SimulationProtein Kinase InhibitorsSignal TransductionXenograft Model Antitumor AssaysAdenineAminoquinolinesAntineoplastic AgentsClass I Phosphatidylinositol 3-KinasesPIK3CD protein, humanProtein Kinase InhibitorspuquitinibAcute myeloid leukemiaCAL-101PI3K signalingPI3Kδpuquitinib

Identifiers

PMID28418085
PMCPMC5497803
OpenAlexW2606253060

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.