Evidence map›Paper›PMID 33664852›Full record

ArticleTheranostics2021

Genome-wide CRISPR/Cas9 knockout screening uncovers a novel inflammatory pathway critical for resistance to arginine-deprivation therapy.

Cheng-Ying Chu, Yi-Ching Lee, Cheng-Han Hsieh, Chi-Tai Yeh, Tsu-Yi Chao, Po-Hung Chen, I-Hsuan Lin, Tsung-Han Hsieh, Jing-Wen Shih, Chia-Hsiung Cheng and 7 more

Open access · goldAbstract read
In one paragraph

Article in Theranostics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

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  15. CRISPR Screen Contributes to Novel Target Discovery in Prostate Cancer.International journal of molecular sciences · 2021
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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

17 authors at 4 institutions in 1 country.

Cheng-Ying ChuTMU Research Center of Cancer Translational Medicine, Taipei Medical University, Taipei 110, Taiwan.
Yi-Ching LeeCRISPR Gene Targeting Core Lab, Taipei Medical University, Taipei 110, Taiwan.
Cheng-Han HsiehTMU Research Center of Cancer Translational Medicine, Taipei Medical University, Taipei 110, Taiwan.
Chi-Tai YehDepartment of Medical Research & Education, Taipei Medical University - Shuang Ho Hospital, New Taipei City.
Tsu-Yi ChaoDepartment of Medical Research & Education, Taipei Medical University - Shuang Ho Hospital, New Taipei City.
Po-Hung ChenInstitute of Biological Chemistry, Academia Sinica, Taipei, Taiwan.
I-Hsuan LinTMU Research Center of Cancer Translational Medicine, Taipei Medical University, Taipei 110, Taiwan.
Tsung-Han HsiehJoint Biobank, Office of Human Research, Taipei Medical University, Taipei, Taiwan.
Jing-Wen ShihTMU Research Center of Cancer Translational Medicine, Taipei Medical University, Taipei 110, Taiwan.
Chia-Hsiung ChengDepartment of Biochemistry and Molecular Cell Biology, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Che-Chang ChangThe Ph.D. Program for Translational Medicine, College of Medical Science and Technology, Taipei Medical University, Taipei 110, Taiwan.
Ping-Sheng LinPh.D. Program for Cancer Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, Taipei 110, Taiwan.
Yuan-Li HuangDepartment of Biotechnology, College of Medical and Health Science, Asia University, Taichung, Taiwan.
Tsung-Ming ChenDepartment and Graduate Institute of Aquaculture, National Kaohsiung University of Science and Technology, Kaohsiung 81157, Taiwan.
Yun YenTMU Research Center of Cancer Translational Medicine, Taipei Medical University, Taipei 110, Taiwan.
David K AnnDepartment of Diabetes and Metabolic Diseases Research, Irell & Manella Graduate School of Biological Sciences, Beckman Research Institute, City of Hope, Duarte, CA, United States.
Hsing-Jien KungTMU Research Center of Cancer Translational Medicine, Taipei Medical University, Taipei 110, Taiwan.
Taipei Medical University · TWAsia University · TWInstitute of Biological Chemistry, Academia Sinica · TWNational Kaohsiung Marine University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Arginine synthesis deficiency due to the suppressed expression of ASS1 (argininosuccinate synthetase 1) represents one of the most frequently occurring metabolic defects of tumor cells. Arginine-deprivation therapy has gained increasing attention in recent years. One challenge of ADI-PEG20 (pegylated ADI) therapy is the development of drug resistance caused by restoration of ASS1 expression and other factors. The goal of this work is to identify novel factors conferring therapy resistance.

Indexed as

AnimalsArginineArgininosuccinate SynthaseBreast NeoplasmsCell Line, TumorChemokine CCL2CRISPR-Cas SystemsDrug Resistance, NeoplasmFemaleGene Knockout TechniquesHumansHydrolasesInflammationMaleMiceMice, Inbred BALB CADI PEG20ArginineArgininosuccinate SynthaseCCL2 protein, humanChemokine CCL2HydrolasesPolyethylene GlycolsTREM1 protein, humanTriggering Receptor Expressed on Myeloid Cells-1ADI resistancearginine starvationCCL2CRISPR/Cas9TREM1

Identifiers

PMID33664852
PMCPMC7914361
OpenAlexW3127072102

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.