Evidence map›Paper›PMID 35090088›Full record

ArticleClinical and translational medicine2022

Disruption of the pentraxin 3/CD44 interaction as an efficient therapy for triple-negative breast cancers.

Yu-Wei Hsiao, Jhih-Ying Chi, Chien-Feng Li, Lei-Yi Chen, Yi-Ting Chen, Hsin-Yin Liang, Yu-Chih Lo, Jhen-Yi Hong, Chin-Pin Chuu, Liang-Yi Hung and 3 more

Open access · goldAbstract read
In one paragraph

Article in Clinical and translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

21 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. 3D-bioprinted adipose-derived stem cell-secreted GAS6Journal of nanobiotechnology · 2026
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Role of long pentraxin PTX3 in cancer.Clinical and experimental medicine · 2023
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Insights into the Relationship between Pentraxin-3 and Cancer.International journal of molecular sciences · 2022
    Review
  19. Article
  20. Article
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

13 authors at 5 institutions in 1 country.

Yu-Wei HsiaoDepartment of Biotechnology and Bioindustry Sciences, College of Bioscience and Biotechnology, National Cheng Kung University, Tainan, Taiwan R. O. C.
Jhih-Ying ChiDepartment of Biotechnology and Bioindustry Sciences, College of Bioscience and Biotechnology, National Cheng Kung University, Tainan, Taiwan R. O. C.
Chien-Feng LiDepartment of Pathology, Chi-Mei Medical Center, Tainan, Taiwan R. O. C.ORCID 0000-0002-9527-7576
Lei-Yi ChenDepartment of Biotechnology and Bioindustry Sciences, College of Bioscience and Biotechnology, National Cheng Kung University, Tainan, Taiwan R. O. C.
Yi-Ting ChenDepartment of Biotechnology and Bioindustry Sciences, College of Bioscience and Biotechnology, National Cheng Kung University, Tainan, Taiwan R. O. C.
Hsin-Yin LiangDepartment of Biotechnology and Bioindustry Sciences, College of Bioscience and Biotechnology, National Cheng Kung University, Tainan, Taiwan R. O. C.
Yu-Chih LoDepartment of Biotechnology and Bioindustry Sciences, College of Bioscience and Biotechnology, National Cheng Kung University, Tainan, Taiwan R. O. C.
Jhen-Yi HongDepartment of Biotechnology and Bioindustry Sciences, College of Bioscience and Biotechnology, National Cheng Kung University, Tainan, Taiwan R. O. C.
Chin-Pin ChuuInstitute of Cellular and System Medicine, National Health Research Institutes, Miaoli County, Taiwan R. O. C.ORCID 0000-0001-7206-7923
Liang-Yi HungDepartment of Biotechnology and Bioindustry Sciences, College of Bioscience and Biotechnology, National Cheng Kung University, Tainan, Taiwan R. O. C.
Jyun-Yi DuDepartment of Biotechnology and Bioindustry Sciences, College of Bioscience and Biotechnology, National Cheng Kung University, Tainan, Taiwan R. O. C.
Wen-Chang ChangGraduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan R. O. C.
Ju-Ming WangDepartment of Biotechnology and Bioindustry Sciences, College of Bioscience and Biotechnology, National Cheng Kung University, Tainan, Taiwan R. O. C.ORCID 0000-0002-1094-860X
National Cheng Kung University · TWChi Mei Medical Center · TWKaohsiung Medical University · TWNational Health Research Institutes · TWTaipei Medical University · TW

Funding

Ministry of Science and Technology, Taiwan 109-2320-B-006-026-MY3Ministry of Science and Technology, Taiwan 110-2320-B-006-053
6 · The paper itself

Abstract

Due to the heterogeneity and high frequency of genome mutations in cancer cells, targeting vital protumour factors found in stromal cells in the tumour microenvironment may represent an ideal strategy in cancer therapy. However, the regulation and mechanisms of potential targetable therapeutic candidates need to be investigated. An in vivo study demonstrated that loss of pentraxin 3 (PTX3) in stromal cells significantly decreased the metastasis and growth of cancer cells. Clinically, our results indicate that stromal PTX3 expression correlates with adverse prognostic features and is associated with worse survival outcomes in triple-negative breast cancer (TNBC). We also found that transforming growth factor beta 1 (TGF-β1) induces PTX3 expression by activating the transcription factor CCAAT/enhancer binding protein delta (CEBPD) in stromal fibroblasts. Following PTX3 stimulation, CD44, a PTX3 receptor, activates the downstream ERK1/2, AKT and NF-κB pathways to specifically contribute to the metastasis/invasion and stemness of TNBC MDA-MB-231 cells. Two types of PTX3 inhibitors were developed to disrupt the PTX3/CD44 interaction and they showed a significant effect on attenuating growth and restricting the metastasis/invasion of MDA-MB-231 cells, suggesting that targeting the PTX3/CD44 interaction could be a new strategy for future TNBC therapies.

Indexed as

C-Reactive ProteinFemaleHumansHyaluronan ReceptorsPentraxinsSerum Amyloid P-ComponentTriple Negative Breast NeoplasmsTumor MicroenvironmentCD44 protein, humanC-Reactive ProteinHyaluronan ReceptorsPentraxinsSerum Amyloid P-ComponentCD44 and tumour microenvironmentNF-κBpentraxin 3 (PTX3)triple-negative breast cancer cells (TNBC)

Identifiers

PMID35090088
PMCPMC8797470
OpenAlexW4210677575

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.