Evidence map›Paper›PMID 34249423›Full record

ArticleAmerican journal of cancer research2021

Mortalin maintains breast cancer stem cells stemness via activation of Wnt/GSK3β/β-catenin signaling pathway.

Bo Wei, Jia Cao, Jin-Hai Tian, Chuan-Yang Yu, Qi Huang, Jing-Jing Yu, Rong Ma, Jia Wang, Fang Xu, Li-Bin Wang

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 19 citations in OpenAlex.

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  15. Wnt Signaling in the Breast: From Development to Disease.Frontiers in cell and developmental biology · 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

10 authors at 1 institution in 1 country.

Bo WeiThe General Hospital of Ningxia Medical University Yinchuan 750004, China.
Jia CaoThe General Hospital of Ningxia Medical University Yinchuan 750004, China.
Jin-Hai TianThe General Hospital of Ningxia Medical University Yinchuan 750004, China.
Chuan-Yang YuThe General Hospital of Ningxia Medical University Yinchuan 750004, China.
Qi HuangThe General Hospital of Ningxia Medical University Yinchuan 750004, China.
Jing-Jing YuThe General Hospital of Ningxia Medical University Yinchuan 750004, China.
Rong MaThe General Hospital of Ningxia Medical University Yinchuan 750004, China.
Jia WangThe General Hospital of Ningxia Medical University Yinchuan 750004, China.
Fang XuNingxia Medical University Yinchuan 750004, China.
Li-Bin WangThe General Hospital of Ningxia Medical University Yinchuan 750004, China.
Ningxia Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous research indicated that mortalin overexpressed in breast cancer and contributed to carcinogenesis. Mortalin was also demonstrated to promote Epithelial-mesenchymal transition (EMT) and was considered as a factor for maintaining the stemness of the cancer stem cells. However, the underlying mechanisms about mortalin maintaining the stemness of breast cancer stem cells (BCSCs) remain unclear. Here, we identified that increased expression of mortalin in breast cancer was associated with poorer overall survival rate. Mortalin was elevated in breast cancer cell lines and BCSC-enriched populations. Additionally, knockdown of mortalin significantly inhibited the cell proliferation, migration and EMT, as well as sphere forming capacity and stemness genes expression. Further study revealed that mortalin promoted EMT and maintained BCSCs stemness via activating the Wnt/GSK3β/β-catenin signaling pathway

Indexed as

breast cancer stem cellsEMTMortalinstemnessWnt/GSK3β/β-catenin signaling pathway

Identifiers

PMID34249423
PMCPMC8263651
OpenAlexW3179281022

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.