Evidence map›Paper›PMID 25328409›Full record

ArticleOncoTargets and therapy2014

Crenolanib, a PDGFR inhibitor, suppresses lung cancer cell proliferation and inhibits tumor growth in vivo.

Ping Wang, Liqiang Song, Hui Ge, Pule Jin, Yifang Jiang, Wenxia Hu, Nan Geng

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
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  8. Analysis of CD74 Occurrence in Oncogenic Fusion Proteins.International journal of molecular sciences · 2023
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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

7 authors at 2 institutions in 1 country.

Ping WangDepartment of Respiratory Medicine, Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, People's Republic of China.
Liqiang SongDepartment of Pathology, School of Basic Medical Sciences, Peking Union Medical College, Beijing, People's Republic of China.
Hui GeDepartment of Respiratory Medicine, Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, People's Republic of China.
Pule JinDepartment of Respiratory Medicine, Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, People's Republic of China.
Yifang JiangDepartment of Respiratory Medicine, Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, People's Republic of China.
Wenxia HuDepartment of Respiratory Medicine, Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, People's Republic of China.
Nan GengDepartment of Respiratory Medicine, Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, People's Republic of China.
Fourth Hospital of Hebei Medical University · CNPeking Union Medical College Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Platelet-derived growth factor (PDGF) and its receptors (PDGFR), including PDGFRα and PDGFRβ, play important roles in tumorigenesis, tumor progression, and the regulation of stromal cell function. Constitutive activation of PDGFR signaling, gene rearrangement, and activating mutations of PDGFR have been identified in various types of human tumors and malignancies. PDGFRα and PDGFRβ belong to the family of type III receptor tyrosine kinases and, upon stimulation, activate downstream signaling cascades. Crenolanib is a specific tyrosine kinase inhibitor that targets and inhibits the kinase activity of PDGFR and the FMS-related tyrosine kinase 3. Its clinical efficacy in several human tumors is currently under investigation in Phase II clinical trials. In this study, we examined the potential role of crenolanib in the treatment of non-small-cell lung cancer (NSCLC). Using A549 cells as a model system, we have shown that crenolanib is capable of suppressing proliferation and inducing apoptosis in a dose-dependent manner. Crenolanib-treated cells have reduced migratory activity in response to inducers of chemotaxis. Furthermore, the in vivo antitumor activity of crenolanib was confirmed in an NSCLC xenograft tumor model. Injection of crenolanib significantly inhibited the growth of tumor mass by inducing apoptosis in tumor cells. Our results provide strong evidence supporting the use of crenolanib as a potential therapeutic agent in treating NSCLC. This work sets a foundation for further development of targeted and personalized therapeutics for lung cancer.

Indexed as

chemotherapynon-small-cell lung cancerplatelet-derived growth factor receptor signalingreceptor tyrosine kinasetargeted therapytyrosine kinase inhibitor

Identifiers

PMID25328409
PMCPMC4196792
OpenAlexW1982463677

What Socratic 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 Socratic graph.