Evidence map›Paper›PMID 30336071›Full record

ArticleCancer biology & therapy2019

FSTL1 enhances chemoresistance and maintains stemness in breast cancer cells via integrin β3/Wnt signaling under miR-137 regulation.

Shaoqiang Cheng, Yuanxi Huang, Chun Lou, Yanxia He, Yue Zhang, Qingyuan Zhang

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 7% 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

68 citing papers in PubMed, 1 synthesis or guideline pooled it, 105 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. High FSTL1 expression promotes bladder cancer progression by enhancing tumor cell migration.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  7. Article
  8. Review
  9. Review
  10. Regulation of Cancer Stem Cells in the Tumor Microenvironment.Cancer heterogeneity and plasticity · 2025
    Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Wnt signaling and tumors (Review).Molecular and clinical oncology · 2024
    Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

8 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 1 country.

Shaoqiang Chenga Department of Breast Surgery , Harbin Medical University Cancer Hospital , Harbin , China.
Yuanxi Huanga Department of Breast Surgery , Harbin Medical University Cancer Hospital , Harbin , China.
Chun Loua Department of Breast Surgery , Harbin Medical University Cancer Hospital , Harbin , China.
Yanxia Heb Department of Clinical Oncology , Harbin Medical University Cancer Hospital , Harbin , China.
Yue Zhangb Department of Clinical Oncology , Harbin Medical University Cancer Hospital , Harbin , China.
Qingyuan Zhangb Department of Clinical Oncology , Harbin Medical University Cancer Hospital , Harbin , China.
Harbin Medical University · CNThird Affiliated Hospital of Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

FSTL1 is a protein coding gene associated with cell signaling pathway regulation and the progression of a variety of disorders. In this study, we hypothesized that FSTL1 increases oncogenesis in breast cancer by enhancing stemness and chemoresistance. RT-PCR and IHC revealed significantly higher FSTL1 mRNA and protein levels in TNBC than in non-TNBC specimens and in breast cancer cell lines. We then found that FSTL1 levels were significantly increased in chemoresistant cells. LIVE/DEAD, MTT cell viability and colony formation assays did in fact demonstrate that FSTL1 is required for CDDP and DOX chemoresistance in breast cancer cell lines. FSTL1 overexpression caused significant elevation of stem cell biomarkers, as well as breast cancer cell proliferation. To determine whether the Wnt/β-catenin signaling pathway is involved in the observed effects of FSTL1, we assessed levels of pathway target. TOP/FOP flash, colony formation, and tumor sphere formation assays indicated that FSTL1 activates Wnt/β-catenin signaling through integrin β3. We then sought to identify a microRNA (miRNA) that regulates FSTL1 activity. Luciferase assays demonstrated that miR-137 reduces FSTL1 mRNA and protein levels. Ultimately, our findings indicate that there is an miR-137/FSTL1/integrin β3/Wnt/β-catenin signaling axis in breast cancer cells that regulates stemness and chemoresistance.

Indexed as

Wnt Signaling Pathwaybeta CateninBreast NeoplasmsCell Line, TumorCisplatinDoxorubicinDrug Resistance, NeoplasmFemaleFollistatin-Related ProteinsHumansImmunohistochemistryIntegrin beta3MicroRNAsNeoplastic Stem CellsRNA, MessengerSignal Transductionbeta CateninCisplatinCTNNB1 protein, humanDoxorubicinFollistatin-Related ProteinsFSTL1 protein, humanIntegrin beta3MicroRNAsMIRN137 microRNA, humanRNA, Messengerbreast cancerchemoresistanceFSTL1integrin β3miR-137stemnessWnt signaling

Identifiers

PMID30336071
PMCPMC6370380
OpenAlexW2896923991

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.