Evidence map›Paper›PMID 35941326›Full record

ArticleHuman cell2022

Exosomal microRNA-551b-3p from bone marrow-derived mesenchymal stromal cells inhibits breast cancer progression via regulating TRIM31/Akt signaling.

Ziang Yang, Bei Xu, Sheng Wu, Weige Yang, Rongkui Luo, Shengkai Geng, Zhaochen Xin, Wen Jin, Xiong Shen, Xixi Gu and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Human cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

10 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

12 authors at 2 institutions in 1 country.

Ziang Yang *Department of General Surgery, Zhongshan Hospital, Fudan University, #180 Fenglin road, Shanghai, 200032, People's Republic of China.
Bei Xu *Department of Oncology, Zhongshan Hospital, Fudan University, Shanghai, People's Republic of China.
Sheng Wu *Department of General Surgery, Qingpu Branch of Zhongshan Hospital, Fudan University, Shanghai, People's Republic of China.
Weige YangDepartment of General Surgery, Zhongshan Hospital, Fudan University, #180 Fenglin road, Shanghai, 200032, People's Republic of China.
Rongkui LuoDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai, People's Republic of China.
Shengkai GengDepartment of Surgery, Fudan University, Shanghai, People's Republic of China.
Zhaochen XinDepartment of General Surgery, Zhongshan Hospital, Fudan University, #180 Fenglin road, Shanghai, 200032, People's Republic of China.
Wen JinDepartment of Oncology, Zhongshan Hospital, Fudan University, Shanghai, People's Republic of China.
Xiong ShenDepartment of Pharmacy, Zhongshan Hospital, Fudan University, Shanghai, People's Republic of China.
Xixi GuDepartment of Integrative Medicine, Zhongshan Hospital, Fudan University, Shanghai, People's Republic of China.
Hongwei ZhangDepartment of General Surgery, Zhongshan Hospital, Fudan University, #180 Fenglin road, Shanghai, 200032, People's Republic of China.
Hong WangDepartment of General Surgery, Zhongshan Hospital, Fudan University, #180 Fenglin road, Shanghai, 200032, People's Republic of China. wang.hong@zs-hospital.sh.cn.ORCID http://orcid.org/0000-0002-2728-5195
Sun Yat-sen University · CNFudan University · CN

Funding

Shanghai Pujiang Talent Program grant no. 18PJD005
6 · The paper itself

Abstract

Mesenchymal stromal cells (MSCs) play an important role in the development of human cancer. Meanwhile, exosomes released by MSCs can mediate cell-cell communication by delivering microRNAs (miRNAs/miRs). Hence, this study aimed to explore the role of bone marrow mesenchymal stromal cell (BMSC)-derived exosomal miR-551b-3p in breast cancer. In this study, we found that upregulation of miR-551b-5p suppressed the proliferation and migration and induced the apoptosis of breast cancer cells via downregulating tripartite motif-containing protein 31 (TRIM31). In addition, miR-551b-5p could be transferred from BMSCs to breast cancer cells via exosomes; BMSC-derived exosomal miR-551b-3p suppressed the proliferation and migration and promoted the apoptosis and oxidative stress of MDA-MB-231 cells via inhibiting TRIM31. Furthermore, a xenograft mouse model was used to explore the role of BMSC-derived exosomal miR-551b-3p in vivo. We found that BMSC-derived exosomal miR-551b-3p inhibited tumor growth in a mouse xenograft model of breast cancer in vivo. Collectively, these findings indicated that BMSC-derived exosomal miR-551b-3p could suppress the development of breast cancer via downregulating TRIM31. Thus, miR-551b-3p could serve as a potential target for the treatment of breast cancer.

Indexed as

Breast NeoplasmsMesenchymal Stem CellsMicroRNAsAnimalsBone MarrowCell ProliferationFemaleHumansMiceProto-Oncogene Proteins c-aktTripartite Motif ProteinsUbiquitin-Protein LigasesMicroRNAsMIRN551B microRNA, humanProto-Oncogene Proteins c-aktTRIM31 protein, humanTripartite Motif ProteinsUbiquitin-Protein LigasesBone marrow mesenchymal stromal cellsBreast cancerExosomemicroRNAsProliferation

Identifiers

PMID35941326
OpenAlexW4290739273

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.