Evidence map›Paper›PMID 31411813›Full record

ArticleCytometry. Part A : the journal of the International Society for Analytical Cytology2020

Yiqi Chutan Tang Reduces Gefitinib-Induced Drug Resistance in Non-Small-Cell Lung Cancer by Targeting Apoptosis and Autophagy.

Jue Zhang, Lingling Sun, Jian Cui, Jing Wang, Xiaomin Liu, Thazin Nwe Aung, Zhipeng Qu, Zhuangzhong Chen, David L Adelson, Lizhu Lin

Open access · hybridAbstract read
In one paragraph

Article in Cytometry. Part A : the journal of the International Society for Analytical Cytology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
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  3. World journal of oncology · 2024
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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

10 authors at 3 institutions in 2 countries.

Jue ZhangFirst Affiliated Hospital, Guangzhou University of Chinese Medicine, Guangzhou, 510000, Guangdong Province, China.
Lingling SunFirst Affiliated Hospital, Guangzhou University of Chinese Medicine, Guangzhou, 510000, Guangdong Province, China.
Jian CuiDepartment of Molecular and Biomedical Science, School of Biological Sciences, The University of Adelaide, Adelaide, South Australia, 5005, Australia.
Jing WangFirst Affiliated Hospital, Guangzhou University of Chinese Medicine, Guangzhou, 510000, Guangdong Province, China.
Xiaomin LiuGuangzhou University of Chinese Medicine, Guangzhou, 510000, Guangdong Province, China.
Thazin Nwe AungDepartment of Molecular and Biomedical Science, School of Biological Sciences, The University of Adelaide, Adelaide, South Australia, 5005, Australia.
Zhipeng QuDepartment of Molecular and Biomedical Science, School of Biological Sciences, The University of Adelaide, Adelaide, South Australia, 5005, Australia.
Zhuangzhong ChenFirst Affiliated Hospital, Guangzhou University of Chinese Medicine, Guangzhou, 510000, Guangdong Province, China.
David L AdelsonDepartment of Molecular and Biomedical Science, School of Biological Sciences, The University of Adelaide, Adelaide, South Australia, 5005, Australia.
Lizhu LinFirst Affiliated Hospital, Guangzhou University of Chinese Medicine, Guangzhou, 510000, Guangdong Province, China.
First Affiliated Hospital of Guangzhou University of Chinese Medicine · CNUniversity of Adelaide · AUGuangzhou University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High incidence and mortality rates for non-small-cell lung cancer (NSCLC) lead to low survival rates. Epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKI) are commonly first prescribed for NSCLC patients with EGFR mutations. However, most patients with sensitizing EGFR mutations become resistant to EGFR-TKI after 9-13 months treatment. Yiqi Chutan Tang (YQCT) has been prescribed as a treatment to this issue for over 20 years. In this report, high-performance liquid chromatography (HPLC) analysis, flow cytometry, western blot analysis, and functional annotation analysis were applied to uncover the molecular mechanisms of YQCT. Our results show the application of YQCT reduces gefitinib-induced drug resistance, induces slight cell cycle arrest, enhances gefitinib-induced apoptosis, and activates the autophagy. These results indicate that at the molecular level YQCT can reduce drug resistance and improve anti-cancer effects when associated with gefitinib, which could be a result of enhancement of apoptosis and autophagy in the EGFR-TKI resistant cells of NSCLC. This research provides a new treatment strategy for patients with EGFR-TKI resistance in NSCLC. © 2019 The Authors. Cytometry Part A published by Wiley Periodicals, Inc. on behalf of International Society for Advancement of Cytometry.

Indexed as

Antineoplastic AgentsApoptosisAutophagyCarcinoma, Non-Small-Cell LungCell ProliferationDrug Resistance, NeoplasmGefitinibHumansLung NeoplasmsMutationProtein Kinase InhibitorsQuinazolinesAntineoplastic AgentsGefitinibProtein Kinase InhibitorsQuinazolinesdrug resistanceepidermal growth factor receptor-tyrosine kinase inhibitorsflow cytometrymolecular mechanismnon-small-cell lung cancer

Identifiers

PMID31411813
PMCPMC7004076
OpenAlexW2969160463

What OpenQuestion 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 OpenQuestion graph.