Evidence map›Paper›PMID 33292235›Full record

ArticleCancer cell international2020

Parthenolide inhibits the growth of non-small cell lung cancer by targeting epidermal growth factor receptor.

Xiaoling Li, Riming Huang, Mingyue Li, Zheng Zhu, Zhiyan Chen, Liao Cui, Hui Luo, Lianxiang Luo

Open access · goldAbstract read
In one paragraph

Article in Cancer cell international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.3field-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

22 citing papers in PubMed, 40 citations in OpenAlex.

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  4. Parthenolide alleviates doxorubicin-induced cardiotoxicity via regulation ofJournal of traditional and complementary medicine · 2025
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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

8 authors at 4 institutions in 2 countries.

Xiaoling LiExperimental Animal Center, Guangdong Medical University, Zhanjiang, 524023, Guangdong, China.
Riming HuangGuangdong Provincial Key Laboratory of Food Quality and Safety, College of Food Science, South China Agricultural University, Guangzhou, 510642, Guangdong, China.
Mingyue LiDepartment of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Zheng ZhuDepartment of Internal Medicine, Division of Hematology/Oncology, University of California Davis, Sacramento, CA, 95817, USA.
Zhiyan ChenThe First Clinical College, Guangdong Medical University, Zhanjiang, 524023, Guangdong, China.
Liao CuiGuangdong Key Laboratory for Research and Development of Natural Drugs, Guangdong Medical University, Zhanjiang, 524023, Guangdong, China.
Hui LuoThe Marine Biomedical Research Institute, Guangdong Medical University, Zhanjiang, 524023, Guangdong, China.
Lianxiang LuoThe Marine Biomedical Research Institute, Guangdong Medical University, Zhanjiang, 524023, Guangdong, China. luolianxiang321@163.com.ORCID http://orcid.org/0000-0002-3391-9713
Guangdong Medical College · CNSouth China Agricultural University · CNUniversity of California, Davis · USUniversity of Pennsylvania · US

Funding

Administration of Traditional Chinese Medicine of Guangdong Province 20201180Basic and Applied Basic Research Program of Guangdong Province 2019A1515110201Department of Education of Guangdong Province (CN) 4SG20138GFund of Southern Marine Science and Engineering GuangdongLaboratory (Zhanjiang) ZJW-2019-007GDNRC [2020]038Natural Science Foundation of Guangdong Province 2016B030309002Science and Technology Special Project of Zhanjiang 2019A01009Scientific Research Foundation of Graduate School of Harbin Medical University: Sino Russian Special Fund (CN) B2019016
6 · The paper itself

Abstract

backgroundEGFR tyrosine kinase inhibitors (TKIs) have been developed for the treatment of EGFR mutated NSCLC. Parthenolide, a natural product of parthenolide, which belongs to the sesquiterpene lactone family and has a variety of biological and therapeutic activities, including anti-cancer effects. However, its effect on non-small cell lung cancer is little known.

methodsThe CCK8 assay and colony formation assays were used to assess cell viability. Flow cytometry was used to measure the cell apoptosis. In silico molecular docking was used to evaluate the binding of parthenolide to EGFR. Network pharmacology analysis was was used to evaluate the key gene of parthenolide target NSCLC. Western blotting was used to evaluate the key proteins involved apoptosis and EGFR signalling. The effect of parthenolide treatment in vivo was determined by using a xenograft mouse model.

resultsIn this study, parthenolide could induce apoptosis and growth inhibition in the EGFR mutated lung cancer cells. Parthenolide also reduces the phosphorylation of EGFR as well as its downstream signaling pathways MAPK/ERK and PI3K/Akt. Molecular docking analysis of EGFR binding site with parthenolide show that the anti-cancer effect of parthenolide against NSCLC is mediated by a strong binding to EGFR. Network pharmacology analysis show parthenolide suppresses NSCLC via inhibition of EGFR expression. In addition, parthenolide inhibits the growth of H1975 xenografts in nude mice, which is associated with the inhibition of the EGFR signaling pathway.

conclusionsTaken together, these results demonstrate effective inhibition of parthenolide in NSCLC cell growth by targeting EGFR through downregulation of ERK and AKT expression, which could be promisingly used for patients carrying the EGFR mutation.

Indexed as

EGFRIn vitroIn vivoNSCLCParthenolide

Identifiers

PMID33292235
PMCPMC7686780
OpenAlexW3108478283

What OpenQuestion holds

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LicenceCC BY
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.