Evidence map›Paper›PMID 32958832›Full record

ArticleOncogene2020

RSK2 protects human breast cancer cells under endoplasmic reticulum stress through activating AMPKα2-mediated autophagy.

Lan-Ya Li, Xi-Sha Chen, Kuan-Song Wang, Yi-Di Guan, Xing-Cong Ren, Dong-Sheng Cao, Xin-Yuan Sun, Ao-Xue Li, Yong-Guang Tao, Yi Zhang and 5 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 34 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

15 authors at 4 institutions in 2 countries.

Lan-Ya Li *Department of Pharmacy, The Second Xiangya Hospital, Central South University, 410011, Changsha, China.
Xi-Sha Chen *Department of Pharmacy, The Second Xiangya Hospital, Central South University, 410011, Changsha, China.
Kuan-Song WangDepartment of Pathology, Xiangya hospital and Department of Pathology, School of Basic Medicine, Central South University, 410078, Changsha, China.
Yi-Di GuanDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, 410011, Changsha, China.
Xing-Cong RenDepartment of Cancer Biology and Toxicology, Department of Pharmacology, College of Medicine, Markey Cancer Center, University of Kentucky, Lexington, KY, 40536, USA.
Dong-Sheng CaoXiangya School of Pharmaceutical Sciences, Central South University, 410008, Changsha, China.
Xin-Yuan SunDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, 410011, Changsha, China.
Ao-Xue LiXiangya School of Pharmaceutical Sciences, Central South University, 410008, Changsha, China.
Yong-Guang TaoCancer Research Institute, School of Basic Medicine, and Key Laboratory of Carcinogenesis and Cancer Invasion, Ministry of Education, Central South University, 410078, Changsha, China.ORCID http://orcid.org/0000-0003-2354-5321
Yi ZhangDepartment of Pharmacology, College of Pharmaceutical Sciences, Soochow University, 410008, Suzhou, China.
Ming-Zhu YinDepartment of Dermatology, Hunan Engineering Research Center of Skin Health and Disease, Hunan Key Laboratory of Skin Cancer and Psoriasis, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Xin-Luan WangTranslational Medicine R&D Center, Institute of Biomedical and Health Engineering, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, 518057, Shenzhen, China.
Ming-Hua WuCancer Research Institute, School of Basic Medicine, and Key Laboratory of Carcinogenesis and Cancer Invasion, Ministry of Education, Central South University, 410078, Changsha, China.ORCID http://orcid.org/0000-0001-5547-907X
Jin-Ming YangDepartment of Cancer Biology and Toxicology, Department of Pharmacology, College of Medicine, Markey Cancer Center, University of Kentucky, Lexington, KY, 40536, USA.
Yan ChengDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, 410011, Changsha, China. yancheng@csu.edu.cn.ORCID http://orcid.org/0000-0002-7905-0443
Central South University · CNUniversity of Kentucky · USChinese Academy of Sciences · CNSoochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy can protect stressed cancer cell by degradation of damaged proteins and organelles. However, the regulatory mechanisms behind this cellular process remain incompletely understood. Here, we demonstrate that RSK2 (p90 ribosomal S6 kinase 2) plays a critical role in ER stress-induced autophagy in breast cancer cells. We demonstrated that the promotive effect of RSK2 on autophagy resulted from directly binding of AMPKα2 in nucleus and phosphorylating it at Thr172 residue. IRE1α, an ER membrane-associated protein mediating unfolded protein response (UPR), is required for transducing the signal for activation of ERK1/2-RSK2 under ER stress. Suppression of autophagy by knockdown of RSK2 enhanced the sensitivity of breast cancer cells to ER stress both in vitro and in vivo. Furthermore, we demonstrated that inhibition of RSK2-mediated autophagy rendered breast cancer cells more sensitive to paclitaxel, a chemotherapeutic agent that induces ER stress-mediated cell death. This study identifies RSK2 as a novel controller of autophagy in tumor cells and suggests that targeting RSK2 can be exploited as an approach to reinforce the efficacy of ER stress-inducing agents against cancer.

Indexed as

AutophagyAMP-Activated Protein KinasesAnimalsAntineoplastic AgentsApoptosisBreast NeoplasmsCell NucleusDrug Resistance, NeoplasmEndoplasmic Reticulum StressEndoribonucleasesFemaleGene Knockdown TechniquesHumansMAP Kinase Signaling SystemMCF-7 CellsMiceAMP-Activated Protein KinasesAntineoplastic AgentsEndoribonucleasesERN1 protein, humanPaclitaxelPRKAA2 protein, humanProtein Serine-Threonine Kinasesribosomal protein S6 kinase, 90kDa, polypeptide 3Ribosomal Protein S6 Kinases, 90-kDa

Identifiers

PMID32958832
OpenAlexW3087675622

What OpenQuestion holds

Textmetadata
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.