Evidence map›Paper›PMID 33478072›Full record

ArticleMolecules (Basel, Switzerland)2021

Arginine Deiminase Induces Immunogenic Cell Death and Is Enhanced by

Zhiying Huang, Haifeng Hu

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
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  5. Targeting HMGB1: An available Therapeutic Strategy for Breast Cancer Therapy.International journal of biological sciences · 2022
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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

2 authors at 2 institutions in 1 country.

Zhiying HuangSchool of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, China.
Haifeng HuShanghai Institute of Pharmaceutical Industry, China State Institute of Pharmaceutical Industry, Shanghai 201203, China.ORCID 0000-0002-4467-9153
Shanghai Institute of Pharmaceutical Industry · CNShanghai Jiao Tong University · CN

Funding

Key Projects of Shanghai in Biomedicine 14431904500
6 · The paper itself

Abstract

The use of arginine deiminase (ADI) for arginine depletion therapy is an attractive anticancer approach. Combination strategies are needed to overcome the resistance of severe types of cancer cells to this monotherapy. In the current study, we report, for the first time, that the antioxidant N-acetylcysteine (NAC), which has been used in therapeutic practices for several decades, is a potent enhancer for targeted therapy that utilizes arginine deiminase. We demonstrated that pegylated arginine deiminase (ADI-PEG 20) induces apoptosis and G0/G1 phase arrest in murine MC38 colorectal cancer cells; ADI-PEG 20 induces Ca

Indexed as

AcetylcysteineColorectal NeoplasmsHydrolasesImmunogenic Cell DeathAnimalsApoptosisBreast NeoplasmsCalreticulinCell Line, TumorHMGB1 ProteinHumansMembrane Potential, MitochondrialMicePolyethylene GlycolsAcetylcysteineADI PEG20arginine deiminaseCalreticulinHMGB1 ProteinHydrolasesPolyethylene Glycolsarginine deiminaseBMDC phagocytosiscell cycle arrestimmunogenic cell deathmitochondrial membrane potentialN-acetylcysteine

Identifiers

PMID33478072
PMCPMC7835909
OpenAlexW3122565767

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.