Evidence map›Paper›PMID 37093249›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2023

Targeting mitochondrial dynamics by AZD5363 in triple-negative breast cancer MDA-MB-231 cell-derived spheres.

Yingqiang Fu, Wei Dong, Yuting Xu, Lin Li, Xin Yu, Yuheng Pang, Liujia Chan, Yuhan Deng, Cheng Qian

Open access · hybridAbstract read
In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2023. 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
3.0field-weighted citation impact, top 8% 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, 13 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

9 authors at 2 institutions in 1 country.

Yingqiang FuDepartment of Breast Cancer Surgery, Harbin Medical University Cancer Hospital, Harbin Medical University, Haping RD NO, 150086, Harbin, Heilongjiang Province, People's Republic of China.
Wei DongDepartment of Breast Cancer Surgery, Harbin Medical University Cancer Hospital, Harbin Medical University, Haping RD NO, 150086, Harbin, Heilongjiang Province, People's Republic of China.
Yuting XuDepartment of Breast Cancer Surgery, Harbin Medical University Cancer Hospital, Harbin Medical University, Haping RD NO, 150086, Harbin, Heilongjiang Province, People's Republic of China.
Lin LiDepartment of Breast Cancer Surgery, Harbin Medical University Cancer Hospital, Harbin Medical University, Haping RD NO, 150086, Harbin, Heilongjiang Province, People's Republic of China.
Xin YuDepartment of Breast Cancer Surgery, Harbin Medical University Cancer Hospital, Harbin Medical University, Haping RD NO, 150086, Harbin, Heilongjiang Province, People's Republic of China.
Yuheng PangDepartment of Breast Cancer Surgery, Harbin Medical University Cancer Hospital, Harbin Medical University, Haping RD NO, 150086, Harbin, Heilongjiang Province, People's Republic of China.
Liujia ChanNorth China Translational Medicine Research Center of Harbin Medical University, Harbin Medical University, Harbin, 150086, Heilongjiang, China.
Yuhan DengDepartment of Breast Cancer Surgery, Harbin Medical University Cancer Hospital, Harbin Medical University, Haping RD NO, 150086, Harbin, Heilongjiang Province, People's Republic of China. 2020021711@hrbmu.edu.cn.
Cheng QianDepartment of Breast Cancer Surgery, Harbin Medical University Cancer Hospital, Harbin Medical University, Haping RD NO, 150086, Harbin, Heilongjiang Province, People's Republic of China. qiancheng@ems.hrbmu.edu.cn.
Third Affiliated Hospital of Harbin Medical University · CNHarbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer stem cells (BCSCs) have been suggested to contribute to chemotherapeutic resistance and disease relapse in breast cancer. Thus, BCSCs represent a promising target in developing novel breast cancer treatment strategies. Mitochondrial dynamics in BCSCs were recently highlighted as an available approach for targeting BCSCs. In this study, a three-dimensional (3D) cultured breast cancer stem cell spheres model was constructed. Mitochondrial dynamics and functions were analyzed by flow cytometry and confocal microscopy. We have demonstrated that the protein levels of FIS 1 and Mitofusin 1 were significantly increased in BCSCs. Moreover, Capivasertib (AZD5363) administration could suppress Mitofusin1 expression in BCSCs. Our use of MitoTracker Orange and annexin V double-staining assay suggested that AZD5363 could induce apoptosis in BCSCs. The sensitivity of stem cell spheres to doxorubicin was investigated by CCK8 assay, and our results indicated that AZD5363 could re-sensitize BCSCs to Doxo. Flow cytometry analysis identified doxo-induced CD44 and CD133 expression in BCSCs could be suppressed by AZD5363. In combination with AZD536, doxo-induced apoptosis in the BCSCs was significantly increased. In conclusion, our study explored, for the first time, that AZD5363 could target mitochondrial dynamics in 3D cultured stem cell spheres (BCSCs) by regulating Mitofusin.

Indexed as

Breast NeoplasmsTriple Negative Breast NeoplasmsCell Line, TumorCell ProliferationFemaleHumansMDA-MB-231 CellsMitochondrial DynamicsNeoplasm Recurrence, LocalPyrimidinesPyrrolescapivasertibPyrimidinesPyrroles3D stem cell spheresAKT inhibitorDrug resistanceMitochondrial fusion

Identifiers

PMID37093249
PMCPMC10497692
OpenAlexW4366821681

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.