Evidence map›Paper›PMID 36903251›Full record

ArticleMolecules (Basel, Switzerland)2023

Novel Dual-Target Kinase Inhibitors of EGFR and ALK Were Designed, Synthesized, and Induced Cell Apoptosis in Non-Small Cell Lung Cancer.

Yangyang Fan, Wei Li, Wenyan Nie, Han Yao, Yuanyuan Ren, Mengxuan Wang, Haoran Nie, Chenxi Gu, Jiadai Liu, Baijiao An

Full text read
In one paragraph

Article in Molecules (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

10 authors.

Yangyang FanSchool of Pharmacy, Binzhou Medical University, Yantai 264003, China.
Wei LiSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.
Wenyan NieSchool of Pharmacy, Binzhou Medical University, Yantai 264003, China.
Han YaoSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.ORCID 0000-0002-4441-0445
Yuanyuan RenSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.
Mengxuan WangSchool of Pharmacy, Binzhou Medical University, Yantai 264003, China.
Haoran NieSchool of Pharmacy, Binzhou Medical University, Yantai 264003, China.
Chenxi GuSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.
Jiadai LiuSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.
Baijiao AnSchool of Pharmacy, Binzhou Medical University, Yantai 264003, China.ORCID 0000-0001-7683-2389

Funding

Baijiao An BY2020KYQD08Baijiao An ZR2021QB172
6 · The paper itself

Abstract

ALK-positive NSCLC coexisting with EGFR mutations is a frequently occurring clinical phenomenon. Targeting ALK and EGFR simultaneously may be an effective way to treat these cancer patients. In this study, we designed and synthesized ten new dual-target EGFR/ALK inhibitors. Among them, the optimal compound

Indexed as

Antineoplastic AgentsCarcinoma, Non-Small-Cell LungLung NeoplasmsApoptosisCell Line, TumorCell ProliferationErbB ReceptorsHumansMutationProtein Kinase InhibitorsReceptor Protein-Tyrosine KinasesAntineoplastic AgentsEGFR protein, humanErbB ReceptorsProtein Kinase InhibitorsReceptor Protein-Tyrosine KinasesALKEGFRkinase inhibitornon-small-cell lung cancer (NSCLC)therapeutic strategy

Identifiers

PMID36903251
PMCPMC10004195

What OpenQuestion holds

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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.