Evidence map›Paper›PMID 32342201›Full record

ArticleJournal of cancer research and clinical oncology2020

Gefitinib sensitization of cisplatin-resistant wild-type EGFR non-small cell lung cancer cells.

Amin Li, Weiya Cao, Xueke Liu, Yinci Zhang, Yongfang Ma, Ruyue Xu, Rongbo Zhang, Xinkuang Liu, Shuping Zhou, Ruikai Wang and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 19 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

12 authors at 1 institution in 1 country.

Amin Li *Medical School, Anhui University of Science and Technology, 168 Taifeng Street, Tianjiaan District, Huainan, 232001, China.
Weiya Cao *Medical School, Anhui University of Science and Technology, 168 Taifeng Street, Tianjiaan District, Huainan, 232001, China.
Xueke Liu *Medical School, Anhui University of Science and Technology, 168 Taifeng Street, Tianjiaan District, Huainan, 232001, China.
Yinci Zhang *Medical School, Anhui University of Science and Technology, 168 Taifeng Street, Tianjiaan District, Huainan, 232001, China.
Yongfang MaMedical School, Anhui University of Science and Technology, 168 Taifeng Street, Tianjiaan District, Huainan, 232001, China.
Ruyue XuMedical School, Anhui University of Science and Technology, 168 Taifeng Street, Tianjiaan District, Huainan, 232001, China.
Rongbo ZhangMedical School, Anhui University of Science and Technology, 168 Taifeng Street, Tianjiaan District, Huainan, 232001, China.
Xinkuang LiuFirst Affiliated Hospital, Anhui University of Science and Technology (Huainan First People's Hospital), Huainan, 232001, China.
Shuping ZhouFirst Affiliated Hospital, Anhui University of Science and Technology (Huainan First People's Hospital), Huainan, 232001, China.
Ruikai WangFirst Affiliated Hospital, Anhui University of Science and Technology (Huainan First People's Hospital), Huainan, 232001, China.
Jiachang LiuFirst Affiliated Hospital, Anhui University of Science and Technology (Huainan First People's Hospital), Huainan, 232001, China.
Xiaolong TangMedical School, Anhui University of Science and Technology, 168 Taifeng Street, Tianjiaan District, Huainan, 232001, China. txljd2006@126.com.
Anhui University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe usual first-line strategy of wild-type EGFR (wtEGFR) non-small cell lung cancer (NSCLC) remains cisplatin-based chemotherapy. However, cisplatin often loses effectiveness because most tumors acquire drug resistance over time. As EGFR is the most important pro-survival/proliferation signal receptor in NSCLC cells, we aimed at investigating whether cisplatin resistance is related to EGFR activation and further evaluating the combined effects of cisplatin/gefitinib (EGFR-tyrosine kinase inhibitor, EGFR-TKI) on cisplatin-resistant wtEGFR NSCLC cells. MATERIALS AND

methodsEGFR activation was analysed in parental and cisplatin-resistant wtEGFR NSCLC cell lines (H358 and H358

resultsEGFR was significantly phosphorylated in cisplatin-resistant wtEGFR NSCLC cells H358

conclusionAbnormal activation of EGFR may induce wtEGFR NSCLC cell resistance to cisplatin. The combined effects of cisplatin/gefitinib suggest that gefitinib, as a combination therapy for patients with cisplatin-resistant wtEGFR NSCLC should be considered.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCarcinoma, Non-Small-Cell LungCell CycleCell Line, TumorCell ProliferationDisease Models, AnimalDose-Response Relationship, DrugDrug Resistance, NeoplasmErbB ReceptorsFemaleGefitinibHumansLung NeoplasmsMAP Kinase Signaling SystemAntineoplastic AgentsEGFR protein, humanErbB ReceptorsGefitinibProtein Kinase InhibitorsProto-Oncogene Proteins c-aktCisplatinGefitinibResistancewtEGFR NSCLC

Identifiers

PMID32342201
PMCPMC7185832
OpenAlexW3018250288

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.