Evidence map›Paper›PMID 34238918›Full record

ArticleCell death discovery2021

Carcinoma associated fibroblasts small extracellular vesicles with low miR-7641 promotes breast cancer stemness and glycolysis by HIF-1α.

Yonglei Liu, Fanli Hua, Yanxia Zhan, Yanfei Yang, Jianfang Xie, Yunfeng Cheng, Feng Li

Open access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

24 citing papers in PubMed, 35 citations in OpenAlex.

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  14. Extracellular vesicles as tools and targets in therapy for diseases.Signal transduction and targeted therapy · 2024
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  19. Special Issue "Advances in Thrombocytopenia".Journal of clinical medicine · 2022
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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

7 authors at 3 institutions in 1 country.

Yonglei LiuResearch Center, Zhongshan Hospital Qingpu Branch, Fudan University, Shanghai, China.
Fanli HuaDepartment of Hematology, Zhongshan Hospital Qingpu Branch, Fudan University, Shanghai, China.
Yanxia ZhanResearch Center, Zhongshan Hospital, Fudan University, Shanghai, China.
Yanfei YangResearch Center, Zhongshan Hospital Qingpu Branch, Fudan University, Shanghai, China.
Jianfang XieResearch Center, Zhongshan Hospital Qingpu Branch, Fudan University, Shanghai, China.
Yunfeng ChengDepartment of Hematology, Zhongshan Hospital Qingpu Branch, Fudan University, Shanghai, China. yfcheng@fudan.edu.cn.
Feng LiDepartment of Hematology, Zhongshan Hospital Qingpu Branch, Fudan University, Shanghai, China. li.feng@zs-hospital.sh.cn.
Fudan University · CNSun Yat-sen University · CNZhongshan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibroblasts play an important role in cancer development and progression. Small extracellular vesicles (sEVs) are one type of extracellular vesicles, which mediate the interaction between cancer-associated fibroblasts and cancer cells by transferring their contents. However, the roles of sEVs from cancer-associated fibroblasts on breast cancer stem cell properties are largely unraveled. The purpose of this study was to explore the roles of sEVs from cancer-associated fibroblasts on breast cancer progression. The miRNA array data showed a different miRNA profile between CAFs sEVs and normal fibroblasts sEVs. By verification using real-time RT-PCR, the data analysis indicated that miR-7641 levels were lower in sEVs from CAFs compared with NFs. The cellular functions were assayed and the results indicated that CAFs derived sEVs with low miR-7641 levels suppressed breast cancer cell survival, glycolysis, and stem cell properties via the HIF-1α pathway. Collectively, these findings indicated that sEVs from CAFs promoted breast cancer stem cell properties and glycolysis via miR-7641/HIF-1α, which was a possible new way for targeting breast cancer.

Identifiers

PMID34238918
PMCPMC8266840
OpenAlexW3178630781

What OpenQuestion holds

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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.