Evidence map›Paper›PMID 33799444›Full record

ArticleInternational journal of molecular sciences2021

6-Azauridine Induces Autophagy-Mediated Cell Death via a p53- and AMPK-Dependent Pathway.

Yeo-Eun Cha, Rackhyun Park, Minsu Jang, Yea-In Park, Ayane Yamamoto, Won Keun Oh, Eun-Ju Lee, Junsoo Park

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-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

9 citing papers in PubMed, 14 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

8 authors at 3 institutions in 1 country.

Yeo-Eun ChaDivision of Biological Science and Technology, Yonsei University, Wonju 26493, Korea.
Rackhyun ParkDivision of Biological Science and Technology, Yonsei University, Wonju 26493, Korea.
Minsu JangDivision of Biological Science and Technology, Yonsei University, Wonju 26493, Korea.
Yea-In ParkDivision of Biological Science and Technology, Yonsei University, Wonju 26493, Korea.ORCID 0000-0002-7851-8470
Ayane YamamotoDivision of Biological Science and Technology, Yonsei University, Wonju 26493, Korea.
Won Keun OhKorea Bioactive Natural Material Bank, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul 08826, Korea.ORCID 0000-0003-0761-3064
Eun-Ju LeeDepartment of Obstetrics and Gynecology, Chung-Ang University School of Medicine, Seoul 06974, Korea.ORCID 0000-0001-9446-1059
Junsoo ParkDivision of Biological Science and Technology, Yonsei University, Wonju 26493, Korea.ORCID 0000-0002-2355-6760
Yonsei University · KRChung-Ang University · KRSeoul National University · KR

Funding

National Research Foundation of Korea 2019R1A2C1006511
6 · The paper itself

Abstract

6-Azauridine (6-AZA), a pyrimidine nucleoside analogue, is known to exhibit both antitumor and antiviral activities. Although 6-AZA was discovered more than 60 years ago, the cellular effects of this compound are yet to be elucidated. Here, we report that 6-AZA regulates autophagy-mediated cell death in various human cancer cells, where 6-AZA treatment activates autophagic flux through the activation of lysosomal function. Furthermore, 6-AZA exhibited cytotoxicity in all cancer cells studied, although the mechanisms of action were diverse. In H460 cells, 6-AZA treatment induced apoptosis, and the extent of the latter could be reduced by treatment with chloroquine (CQ), a lysosomal inhibitor. However, 6-AZA treatment resulted in cell cycle arrest in H1299 cells, which could not be reversed by CQ. The cytotoxicity associated with 6-AZA treatment could be linearly correlated to the degree of autophagy-mediated cell death. In addition, we demonstrated that the cytotoxic effect of 6-AZA was dependent on AMPK and p53. These results collectively indicate that autophagy-mediated cell death triggered by 6-AZA contributes to its antitumor effect.

Indexed as

AMP-Activated Protein Kinase KinasesAntineoplastic AgentsApoptosisAutophagic Cell DeathAutophagyAzauridineCell Line, TumorCell ProliferationCell SurvivalChloroquineDrug SynergismHumansLysosomesNeoplasmsProtein KinasesSignal TransductionAMP-Activated Protein Kinase KinasesAntineoplastic AgentsAzauridineChloroquineProtein KinasesTumor Suppressor Protein p536-azauridineautophagic fluxautophagyautophagy-mediated cell death

Identifiers

PMID33799444
PMCPMC8000275
OpenAlexW3136094055

What OpenQuestion holds

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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.