Evidence map›Paper›PMID 32397306›Full record

ArticleNutrients2020

L-Ascorbic Acid Inhibits Breast Cancer Growth by Inducing IRE/JNK/CHOP-Related Endoplasmic Reticulum Stress-Mediated p62/SQSTM1 Accumulation in the Nucleus.

Youn Kyung Choi, Jung-Il Kang, Sanghoon Han, Young Ree Kim, Jaemin Jo, Yong Woo Kang, Do Ryeon Choo, Jin Won Hyun, Young Sang Koh, Eun-Sook Yoo and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
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  11. p62: Friend or Foe? Evidences forInternational journal of molecular sciences · 2020
    Review
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

11 authors at 2 institutions in 1 country.

Youn Kyung ChoiDepartment of Medicine, School of Medicine, Jeju National University 102 Jejudaehakno, Jeju 63243, Korea.
Jung-Il KangDepartment of Medicine, School of Medicine, Jeju National University 102 Jejudaehakno, Jeju 63243, Korea.
Sanghoon HanDepartment of Medicine, School of Medicine, Jeju National University 102 Jejudaehakno, Jeju 63243, Korea.
Young Ree KimDepartment of Medicine, School of Medicine, Jeju National University 102 Jejudaehakno, Jeju 63243, Korea.
Jaemin JoDepartment of Medicine, School of Medicine, Jeju National University 102 Jejudaehakno, Jeju 63243, Korea.
Yong Woo KangDepartment of Medicine, School of Medicine, Jeju National University 102 Jejudaehakno, Jeju 63243, Korea.
Do Ryeon ChooDepartment of Medicine, School of Medicine, Jeju National University 102 Jejudaehakno, Jeju 63243, Korea.
Jin Won HyunDepartment of Medicine, School of Medicine, Jeju National University 102 Jejudaehakno, Jeju 63243, Korea.
Young Sang KohDepartment of Medicine, School of Medicine, Jeju National University 102 Jejudaehakno, Jeju 63243, Korea.
Eun-Sook YooDepartment of Medicine, School of Medicine, Jeju National University 102 Jejudaehakno, Jeju 63243, Korea.
Hee-Kyoung KangDepartment of Medicine, School of Medicine, Jeju National University 102 Jejudaehakno, Jeju 63243, Korea.
Jeju National University · KRJeju TechnoPark · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anticancer effects of L-ascorbic acid (Vitamin C, L-AA) have been reported in various types of cancers. L-AA intake reduces breast cancer recurrence and mortality; however, the role of L-AA in the treatment of breast cancer remains poorly understood. In this study, we investigated the effect and mechanism action of L-AA on breast cancer growth. L-AA inhibited the growth of breast cancer cells by inducing apoptotic cell death at the evaluated treatment concentrations without affecting normal cells. Moreover, L-AA induces autophagosome formation via regulation of mammalian target of rapamycin (

Indexed as

Ascorbic AcidBreast NeoplasmsCell DeathCell Line, TumorCell NucleusEndoplasmic Reticulum StressEndoribonucleasesFemaleHumansJNK Mitogen-Activated Protein KinasesRNA-Binding ProteinsSequestosome-1 ProteinSignal TransductionTranscription Factor CHOPAscorbic AcidDDIT3 protein, humanEndoribonucleasesJNK Mitogen-Activated Protein KinasesP62 protein, humanRNA-Binding ProteinsSequestosome-1 ProteinSQSTM1 protein, humanTranscription Factor CHOPautophagybreast cancerER stressIRE–JNK–CHOP signalingL-ascorbic acidp62/SQSTM1

Identifiers

PMID32397306
PMCPMC7284633
OpenAlexW3021676749

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.