Evidence map›Paper›PMID 33791071›Full record

ArticleOxidative medicine and cellular longevity2021

Pegylated Recombinant Human Arginase 1 Induces Autophagy and Apoptosis via the ROS-Activated AKT/mTOR Pathway in Bladder Cancer Cells.

Zhuyun Zhao, Peng Zhang, Wei Li, Dengchuan Wang, Changneng Ke, Yueming Liu, James Chung-Man Ho, Paul Ning-Man Cheng, Shi Xu

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 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
1.9field-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, 24 citations in OpenAlex.

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  16. Methylation of CALCA and CALCB in Pancreatic Ductal Adenocarcinoma.Oxidative medicine and cellular longevity · 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

9 authors at 3 institutions in 2 countries.

Zhuyun ZhaoDepartment of Burn and Plastic Surgery, Shenzhen Longhua District Central Hospital, Affiliated Central Hospital of Shenzhen Longhua District, Guangdong Medical University, Shenzhen, Guangdong, China.ORCID https://orcid.org/0000-0002-3759-6130
Peng ZhangDepartment of Pharmacy, Shenzhen Luohu People's Hospital, Shenzhen, Guangdong, China.ORCID https://orcid.org/0000-0002-9092-9563
Wei LiDepartment of Urology, Shenzhen Longhua District Central Hospital, Affiliated Central Hospital of Shenzhen Longhua District, Guangdong Medical University, Shenzhen, Guangdong, China.ORCID https://orcid.org/0000-0001-6590-9918
Dengchuan WangOffice of Medical Ethics, Shenzhen Longhua District Central Hospital, Affiliated Central Hospital of Shenzhen Longhua District, Guangdong Medical University, Shenzhen, Guangdong, China.ORCID https://orcid.org/0000-0003-2737-3336
Changneng KeDepartment of Burn and Plastic Surgery, Shenzhen Longhua District Central Hospital, Affiliated Central Hospital of Shenzhen Longhua District, Guangdong Medical University, Shenzhen, Guangdong, China.ORCID https://orcid.org/0000-0003-4646-1278
Yueming LiuDepartment of Burn and Plastic Surgery, Shenzhen Longhua District Central Hospital, Affiliated Central Hospital of Shenzhen Longhua District, Guangdong Medical University, Shenzhen, Guangdong, China.ORCID https://orcid.org/0000-0002-3176-4543
James Chung-Man HoDivision of Respiratory Medicine, Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Pokfulam, Hong Kong SAR, China.ORCID https://orcid.org/0000-0003-4499-5284
Paul Ning-Man ChengBio-Cancer Treatment International, 511-513, Bioinformatics Building, Hong Kong Science Park, Tai Po, Hong Kong SAR, China.
Shi XuDepartment of Burn and Plastic Surgery, Shenzhen Longhua District Central Hospital, Affiliated Central Hospital of Shenzhen Longhua District, Guangdong Medical University, Shenzhen, Guangdong, China.ORCID https://orcid.org/0000-0002-2178-5666
Guangdong Medical College · CNQueen Mary Hospital · CNShenzhen Luohu People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bladder cancer is one of the most commonly diagnosed cancers worldwide, especially in males. Current therapeutic interventions, including surgery, radiation therapy, chemotherapy, and immunotherapy, have not been able to improve the clinical outcome of bladder cancer patients with satisfaction. Recombinant human arginase (rhArg, BCT-100) is a novel agent with great anticancer effects on arginine-auxotrophic tumors. However, the effects of BCT-100 on bladder cancer remain unclear. In this study, the

Indexed as

Signal TransductionAnimalsApoptosisArginaseArginineAutophagyCell Line, TumorFemaleHumansMembrane Potential, MitochondrialMiceMice, Inbred BALB CMice, NudeMitochondriaNeoplasm ProteinsProto-Oncogene Proteins c-aktArginaseArginineBCT-100Neoplasm ProteinsProto-Oncogene Proteins c-aktReactive Oxygen SpeciesRecombinant ProteinsTOR Serine-Threonine Kinases

Identifiers

PMID33791071
PMCPMC7996046
OpenAlexW3185728005

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.