Evidence map›Paper›PMID 28378571›Full record

ArticleJournal of Zhejiang University. Science. B

Protein tyrosine phosphatase 1B expression contributes to the development of breast cancer.

Shi-Chong Liao, Jin-Xin Li, Li Yu, Sheng-Rong Sun

Open access · bronzeAbstract read
In one paragraph

Article in Journal of Zhejiang University. Science. B. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Protein Tyrosine Phosphatases: Mechanisms in Cancer.International journal of molecular sciences · 2021
    Review
  6. Review
  7. Article
  8. Review
  9. Pyruvate Kinase M2: a Metabolic Bug in Re-Wiring the Tumor Microenvironment.Cancer microenvironment : official journal of the International Cancer Microenvironment Society · 2019
    Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. 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

4 authors at 2 institutions in 1 country.

Shi-Chong LiaoDepartment of Thyroid and Breast Surgery, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Jin-Xin LiDepartment of Teaching Administration, Wuhan University School of Medicine, Wuhan 430071, China.
Li YuIntensive Care Unit, the Central Hospital of Wuhan, Wuhan 430014, China.
Sheng-Rong SunDepartment of Thyroid and Breast Surgery, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Wuhan University · CNCentral Hospital of Wuhan · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The protein tyrosine phosphatase 1B (PTP1B) is an important regulator of metabolism. The relationship between PTP1B and tumors is quite complex. The purpose of this study is to explore the expression pattern and role of PTP1B in breast cancer. The expression of PTP1B was detected in 67 samples of breast cancer tissue by Western blot. Cell growth assay, Transwell migration assay, and Scratch motility assay were used to examine the proliferation and migration of MCF-7 with and without PTP1B. The total levels and phosphorylated levels of signal transduction and activator of transcription 3 (STAT3) and the expression of C-C motif chemokine ligand 5 (CCL5) were also examined by Western blot. PTP1B was overexpressed in over 70% of breast cancer tissues, correlating with patients with estrogen receptor (ER)-negative, progesterone receptor (PR)-negative, and human epidermal growth factor receptor 2 (HER2)-positive tumors. The data also showed that both tumor size and lymph node metastasis were significantly higher in patients with a higher level of PTP1B. The proliferation and migration of MCF-7 cells were found to be inhibited after knocking down the gene of PTP1B. Our data also showed that PTP1B could up-regulate the dephosphorylated level of STAT3, which could increase the expression of CCL5. These phenomena indicated that PTP1B may play a crucial role in the development of breast cancer.

Indexed as

Breast NeoplasmsCell MovementCell ProliferationChemokine CCL5FemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansLymphatic MetastasisMCF-7 CellsPhosphorylationProtein Tyrosine Phosphatase, Non-Receptor Type 1STAT3 Transcription FactorCCL5 protein, humanChemokine CCL5Protein Tyrosine Phosphatase, Non-Receptor Type 1PTPN1 protein, humanSTAT3 protein, humanSTAT3 Transcription FactorProtein tyrosine phosphatase 1B (PTP1B); Signal transduction and activator of transcription 3 (STAT3); Breast cancer; Tumorigenesis

Identifiers

PMID28378571
PMCPMC5394098
OpenAlexW2606661643

What OpenQuestion holds

Textmetadata
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Registered trials

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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.