Evidence map›Paper›PMID 37928274›Full record

ArticleInternational journal of biological sciences2023

Glutamine metabolism controls amphiregulin-facilitated chemoresistance to cisplatin in human chondrosarcoma.

Yu-Ying Wu, Yat-Yin Law, Yu-Wen Huang, Nguyen Bao Tran, Chih-Yang Lin, Chao-Yang Lai, Yuan-Li Huang, Chun-Hao Tsai, Chih-Yuan Ko, Ming-Chih Chou and 4 more

Open access · goldAbstract read
In one paragraph

Article in International journal of biological sciences, 2023. 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
3.9field-weighted citation impact, top 6% 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, 15 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

14 authors at 6 institutions in 3 countries.

Yu-Ying WuInstitute of Medicine, Chung Shan Medical University, Taichung, Taiwan.
Yat-Yin LawSchool of Medicine, Chung Shan Medical University, Taichung, Taiwan.
Yu-Wen HuangDepartment of Pharmacology, School of Medicine, China Medical University, Taichung, Taiwan.
Nguyen Bao TranGraduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan.
Chih-Yang LinTranslational Medicine Center, Shin-Kong Wu Ho-Su Memorial Hospital, Taipei, Taiwan.
Chao-Yang LaiDepartment of Medical Laboratory Science and Biotechnology, College of Medical and Health Science, Asia University, Taichung, Taiwan.
Yuan-Li HuangDepartment of Medical Laboratory Science and Biotechnology, College of Medical and Health Science, Asia University, Taichung, Taiwan.
Chun-Hao TsaiDepartment of Sports Medicine, College of Health Care, China Medical University, Taichung, Taiwan.
Chih-Yuan KoGraduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan.
Ming-Chih ChouInstitute of Medicine, Chung Shan Medical University, Taichung, Taiwan.
Wei-Chien HuangGraduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan.
Fang-Ju ChengGraduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan.
Yi-Chin FongDepartment of Sports Medicine, College of Health Care, China Medical University, Taichung, Taiwan.
Chih-Hsin TangDepartment of Pharmacology, School of Medicine, China Medical University, Taichung, Taiwan.
China Medical University Hospital · TWChina Medical University · TWChung Shan Medical University Hospital · TWAsia University · TWChung Shan Medical University · TWMemorial Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chondrosarcoma is the second most common type of bone cancer. At present, the most effective clinical course of action is surgical resection. Cisplatin is the chemotherapeutic medication most widely used for the treatment of chondrosarcoma; however, its effectiveness is severely hampered by drug resistance. In the current study, we compared cisplatin-resistant chondrosarcoma SW1353 cells with their parental cells via RNA sequencing. Our analysis revealed that glutamine metabolism is highly activated in resistant cells but glucose metabolism is not. Amphiregulin (AR), a ligand of the epidermal growth factor receptor, enhances glutamine metabolism and supports cisplatin resistance in human chondrosarcoma by promoting NADPH production and inhibiting reactive oxygen species (ROS) accumulation. The MEK, ERK, and NrF2 signaling pathways were shown to regulate AR-mediated alanine-serine-cysteine transporter 2 (ASCT2; also called SLC1A5) and glutaminase (GLS) expression as well as glutamine metabolism in cisplatin-resistant chondrosarcoma. The knockdown of AR expression in cisplatin-resistant chondrosarcoma cells was shown to reduce the expression of SLC1A5 and GLS

Indexed as

Bone NeoplasmsChondrosarcomaAmino Acid Transport System ASCAmphiregulinCell Line, TumorCisplatinDrug Resistance, NeoplasmGlutamineHumansMinor Histocompatibility AntigensAmino Acid Transport System ASCAmphiregulinCisplatinGlutamineMinor Histocompatibility AntigensSLC1A5 protein, humanamphiregulinchondrosarcomacisplatinGLSSLC1A5

Identifiers

PMID37928274
PMCPMC10620823
OpenAlexW4387739863

What OpenQuestion holds

Textmetadata
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.