Evidence map›Paper›PMID 33782541›Full record

ArticleActa pharmacologica Sinica2022

SAF-248, a novel PI3Kδ-selective inhibitor, potently suppresses the growth of diffuse large B-cell lymphoma.

Xi Zhang, Yu-Ting Duan, Yi Wang, Xing-Dong Zhao, Yi-Ming Sun, Dong-Ze Lin, Yi Chen, Yu-Xiang Wang, Zu-Wen Zhou, Yan-Xin Liu and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Targeting MYC-driven lymphoma: lessons learned and future directions.Cancer drug resistance (Alhambra, Calif.) · 2023
    Review
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

14 authors at 4 institutions in 1 country.

Xi ZhangDivision of Anti-tumor Pharmacology, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Yu-Ting DuanDivision of Anti-tumor Pharmacology, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Yi WangDivision of Anti-tumor Pharmacology, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Xing-Dong ZhaoFochon Pharmaceuticals, Ltd., Chongqing, 404100, China.
Yi-Ming SunDivision of Anti-tumor Pharmacology, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Dong-Ze LinDivision of Anti-tumor Pharmacology, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Yi ChenDivision of Anti-tumor Pharmacology, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Yu-Xiang WangDivision of Anti-tumor Pharmacology, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Zu-Wen ZhouFochon Pharmaceuticals, Ltd., Chongqing, 404100, China.
Yan-Xin LiuFochon Pharmaceuticals, Ltd., Chongqing, 404100, China.
Li-Hua JiangFochon Pharmaceuticals, Ltd., Chongqing, 404100, China.
Mei-Yu GengUniversity of Chinese Academy of Sciences, Beijing, 100049, China. mygeng@simm.ac.cn.
Jian DingUniversity of Chinese Academy of Sciences, Beijing, 100049, China. jding@simm.ac.cn.
Ling-Hua MengDivision of Anti-tumor Pharmacology, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China. lhmeng@simm.ac.cn.
Fosun Pharma (China) · CNShanghai Institute of Materia Medica · CNUniversity of Chinese Academy of Sciences · CNChinese Academy of Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PI3Kδ is expressed predominately in leukocytes and overexpressed in B-cell-related malignances. PI3Kδ has been validated as a promising target for cancer therapy, and specific PI3Kδ inhibitors were approved for clinical practice. However, the substantial toxicity and relatively low efficacy as a monotherapy in diffuse large B-cell lymphoma (DLBCL) limit their clinical use. In this study, we described a novel PI3Kδ inhibitor SAF-248, which exhibited high selectivity for PI3Kδ (IC

Indexed as

AnimalsAntineoplastic AgentsCell ProliferationCells, CulturedCell SurvivalClass I Phosphatidylinositol 3-KinasesDose-Response Relationship, DrugDrug Screening Assays, AntitumorFemaleHumansLymphoma, Large B-Cell, DiffuseMiceMice, Inbred BALB CMice, NudeMolecular StructureNeoplasms, ExperimentalAntineoplastic AgentsClass I Phosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsPIK3CD protein, humancombination therapydiffuse large B-cell lymphomaPI3K/AKT/mTORPI3Kδresistance

Identifiers

PMID33782541
PMCPMC8724319
OpenAlexW3152481161

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.