Evidence map›Paper›PMID 29968849›Full record

ArticleActa pharmacologica Sinica2018

Identification of compound D2923 as a novel anti-tumor agent targeting CSF1R.

Ying-Qiang Liu, Ya-Nan Wang, Xiao-Yun Lu, Lin-Jiang Tong, Yan Li, Tao Zhang, Qiu-Ju Xun, Fang Feng, Yu-Zhe Chen, Yi Su and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

10 citing papers in PubMed, 20 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

17 authors at 4 institutions in 1 country.

Ying-Qiang LiuSchool of Life Science, Shanghai University, 200444, Shanghai, China.
Ya-Nan WangState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 201203, Shanghai, China.
Xiao-Yun LuSchool of Pharmacy, Jinan University, No. 601 Huangpu Avenue, 510632, West Guangzhou, China.
Lin-Jiang TongState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 201203, Shanghai, China.
Yan LiState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 201203, Shanghai, China.
Tao ZhangState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 201203, Shanghai, China.
Qiu-Ju XunSchool of Pharmacy, University of Chinese Academy of Sciences, 100049, Beijing, China.
Fang FengState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 201203, Shanghai, China.
Yu-Zhe ChenState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 201203, Shanghai, China.
Yi SuState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 201203, Shanghai, China.
Yan-Yan ShenState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 201203, Shanghai, China.
Yi ChenState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 201203, Shanghai, China.
Mei-Yu GengState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 201203, Shanghai, China.
Ke DingSchool of Pharmacy, Jinan University, No. 601 Huangpu Avenue, 510632, West Guangzhou, China.
Yan-Li LiSchool of Life Science, Shanghai University, 200444, Shanghai, China. liyanli@shu.edu.cn.
Hua XieState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 201203, Shanghai, China. hxie@simm.ac.cn.
Jian DingState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 201203, Shanghai, China. jding@simm.ac.cn.
Shanghai Institute of Materia Medica · CNChinese Academy of Sciences · CNUniversity of Chinese Academy of Sciences · CNJinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colony-stimulating factor 1 receptor (CSF1R) plays a critical role in promoting tumor progression in various types of tumors. Here, we identified D2923 as a novel and selective inhibitor of CSF1R and explored its antitumor activity both in vitro and in vivo. D2923 potently inhibited CSF1R in vitro kinase activity with an IC

Indexed as

AnimalsAntineoplastic AgentsApoptosisCell Line, TumorCell ProliferationG1 Phase Cell Cycle CheckpointsHumansLeukemia, MyeloidMacrophagesMaleMiceMice, Inbred BALB CProtein Kinase InhibitorsPyrimidinonesRAW 264.7 CellsReceptor, Macrophage Colony-Stimulating FactorAntineoplastic AgentsCSF1R protein, humanCsf1r protein, mouseProtein Kinase InhibitorsPyrimidinonesReceptor, Macrophage Colony-Stimulating FactorReceptors, Granulocyte-Macrophage Colony-Stimulating FactorCSF-1Rmacrophagemyeloid leukemiasmall-molecule inhibitor

Identifiers

PMID29968849
PMCPMC6289367
OpenAlexW2809739285

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.