Evidence map›Paper›PMID 25120757›Full record

ArticleInternational journal of clinical and experimental pathology2014

Propranolol enhanced adipogenesis instead of induction of apoptosis of hemangiomas stem cells.

Xiaorong Ma, Tinghui Zhao, Tianxiang Ouyang, Shujia Xin, Yueting Ma, Mengling Chang

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Observational
  2. Article
  3. Article
  4. β-Adrenoceptors in Cancer: Old Players and New Perspectives.Handbook of experimental pharmacology · 2024
    Review
  5. Review
  6. Review
  7. Article
  8. Propranolol inhibits stemness of hemangioma through Jagged1.Annals of translational medicine · 2021
    Article
  9. Article
  10. Article
  11. Article
  12. Progress in the treatment of infantile hemangioma.Annals of translational medicine · 2019
    Review
  13. Article
  14. Article
  15. Combination of propranolol and sclerotherapy for treatment of infantile parotid hemangiomas.International journal of clinical and experimental medicine · 2015
    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

6 authors at 2 institutions in 1 country.

Xiaorong MaDepartment of Plastic and Reconstructive Surgery, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine Shanghai, China.
Tinghui ZhaoDepartment of Plastic and Reconstructive Surgery, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine Shanghai, China.
Tianxiang OuyangDepartment of Plastic and Reconstructive Surgery, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine Shanghai, China.
Shujia XinDepartment of Nursing, Huadong Hospital, Shanghai Fudan University Shanghai, China.
Yueting MaDepartment of Plastic and Reconstructive Surgery, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine Shanghai, China.
Mengling ChangDepartment of Plastic and Reconstructive Surgery, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine Shanghai, China.
XinHua Hospital · CNHuadong Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Propranolol has been widely used in treating infantile hemangiomas (IHs). But recurrence of IHs was found in some cases on cessation of propranolol treatment. The other is that Chinese individuals reacted to propranolol differently from American Whites. Whether the difference of sensitivity is due to the β adrenoceptor (β-AR) expression pattern of hemangioma initiating cells remains unclear. In the present study, we isolated hemangioma-derived stem cells (hemSCs) from proliferative IHs and analyzed the biological characteristics and β-AR expression pattern of hemSCs by immunostaining, Western blotting and multilineage differentiation assay as well. We also tested the effects of propranolol on hemSCs by evaluating VEGF expression, proliferation and apoptosis related parameters. Our results indicated that CD133(+) hemSCs located pre-vascular in proiferative IH tissues. Both β1 and β2-AR were expressed, while β2-AR was dominant on hemSCs. Propranolol at 100-150 μM inhibited proliferation of hemSCs, not did 50 μM. Propranolol down-regulated VEGF expression of hemSCs, instead of inducing apoptosis. The adipogenic potential was enhanced by propranolol. Therefore, our current results suggested propranolol could not induce apoptosis of hemSCs, but played a curative role though suppressing VEGF synthesis and enhancement of adipogenesis of hemSCs. Our results might partially provide the insight of mechanism of relapse in some cases on cessation of propranolol treatment.

Indexed as

AdipogenesisAntineoplastic AgentsApoptosisBlotting, WesternCell DifferentiationCells, CulturedDrug Resistance, NeoplasmFemaleHemangiomaHumansImmunohistochemistryInfantInfant, NewbornMaleNeoplasm Recurrence, LocalNeoplastic Stem CellsAntineoplastic AgentsPropranololReceptors, Adrenergic, betahemangioma-stem cellsPropranololrelapseβ adrenoceptor

Identifiers

PMID25120757
PMCPMC4128992
OpenAlexW203647668

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.