Evidence map›Paper›PMID 36759727›Full record

ArticleBritish journal of cancer2023

Manassantin A inhibits tumour growth under hypoxia through the activation of chaperone-mediated autophagy by modulating Hsp90 activity.

Jun-Kyu Byun, Sun Hee Lee, Eui Jung Moon, Myo-Hyeon Park, Hyeonha Jang, Douglas H Weitzel, Hyun-Hwi Kim, Nikita Basnet, Do-Yeon Kwon, Chen-Ting Lee and 8 more

Open access · greenAbstract read
In one paragraph

Article in British journal of cancer, 2023. 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
1.7field-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

7 citing papers in PubMed, 11 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

18 authors at 6 institutions in 3 countries.

Jun-Kyu ByunCollege of Pharmacy, Kyungpook National University, 80 Daehak-ro, Buk-gu, 41566, Daegu, Republic of Korea.
Sun Hee LeeCollege of Pharmacy, Kyungpook National University, 80 Daehak-ro, Buk-gu, 41566, Daegu, Republic of Korea.
Eui Jung MoonMRC Oxford Institute for Radiation Oncology, Department of Oncology, University of Oxford, Headington, OX3 7DQ, UK.
Myo-Hyeon ParkCollege of Pharmacy, Kyungpook National University, 80 Daehak-ro, Buk-gu, 41566, Daegu, Republic of Korea.
Hyeonha JangCollege of Pharmacy, Kyungpook National University, 80 Daehak-ro, Buk-gu, 41566, Daegu, Republic of Korea.
Douglas H WeitzelDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC, 27710, USA.
Hyun-Hwi KimCollege of Pharmacy and Gachon Institute of Pharmaceutical Sciences, Gachon University, Incheon, 21936, Republic of Korea.
Nikita BasnetCollege of Pharmacy, Kyungpook National University, 80 Daehak-ro, Buk-gu, 41566, Daegu, Republic of Korea.
Do-Yeon KwonDepartment of Chemistry, Duke University, Durham, NC, 27708, USA.
Chen-Ting LeeDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC, 27710, USA.
Tesia N StephensonDepartment of Chemistry, Duke University, Durham, NC, 27708, USA.
Ji-Hak JeongCollege of Pharmacy, Kyungpook National University, 80 Daehak-ro, Buk-gu, 41566, Daegu, Republic of Korea.
Bhargav A PatelDepartment of Chemistry and Biochemistry, University of Notre Dame, South Bend, IN, 46556, USA.
Sung Jean ParkCollege of Pharmacy and Gachon Institute of Pharmaceutical Sciences, Gachon University, Incheon, 21936, Republic of Korea.
Jen-Tsan ChiDepartment of Molecular Genetics & Microbiology, Duke University Medical Center, Durham, NC, 27710, USA.ORCID http://orcid.org/0000-0003-3433-903X
Mark W DewhirstDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC, 27710, USA.
Jiyong HongDepartment of Chemistry, Duke University, Durham, NC, 27708, USA. jiyong.hong@duke.edu.ORCID http://orcid.org/0000-0002-5253-0949
You Mie LeeCollege of Pharmacy, Kyungpook National University, 80 Daehak-ro, Buk-gu, 41566, Daegu, Republic of Korea. lym@knu.ac.kr.ORCID http://orcid.org/0000-0002-5756-7169
Kyungpook National University · KRDuke University · USDuke Medical Center · USGachon University · KRUniversity of Notre Dame · USUniversity of Oxford · GB

Funding

Medical Research Council MC_UU_00001/11
6 · The paper itself

Abstract

backgroundChaperon-mediated autophagy (CMA) has taken on a new emphasis in cancer biology. However, the roles of CMA in hypoxic tumours are poorly understood. We investigated the anti-tumour effects of the natural product ManA through the activation of CMA in tumour progression under hypoxia.

methodsThe effect of ManA on CMA activation was assessed in mouse xenograft models and cells. The gene expressions of HIF-1α, HSP90AA1, and transcription factor EB (TFEB) were analysed using The Cancer Genome Atlas (TCGA) datasets to assess the clinical relevance of CMA.

resultsManA activates photoswitchable CMA reporter activity and inhibits Hsp90 chaperone function by disrupting the Hsp90/F

conclusionsManA-induced CMA activation by modulating Hsp90 under hypoxia induces HIF-1α degradation and reduces tumour growth. Thus, inducing CMA activity by targeting Hsp90 may be a promising therapeutic strategy against hypoxic tumours.

Indexed as

Chaperone-Mediated AutophagyLung NeoplasmsAnimalsAutophagyHSP90 Heat-Shock ProteinsHumansHypoxiaLignansMiceMolecular ChaperonesHSP90 Heat-Shock ProteinsLignansmanassantin AMolecular Chaperones

Identifiers

PMID36759727
PMCPMC10070431
OpenAlexW4319662800

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.