Evidence map›Paper›PMID 22640261›Full record

ArticleBMC cancer2012

Methylseleninic acid restricts tumor growth in nude mice model of metastatic breast cancer probably via inhibiting angiopoietin-2.

Xiaojing Wu, Yidi Zhang, Zengyang Pei, Si Chen, Xu Yang, Yin Chen, Degui Lin, Runlin Z Ma

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2012. 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
1.2field-weighted citation impact, top 20% 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, 28 citations in OpenAlex.

  1. Review
  2. Review
  3. Antitumor Effects of Selenium.International journal of molecular sciences · 2021
    Review
  4. Review
  5. Selenium Compounds as Novel Potential Anticancer Agents.International journal of molecular sciences · 2021
    Review
  6. Article
  7. Article
  8. Role of AQP9 in transport of monomethyselenic acid and selenite.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2017
    Article
  9. Novel Methylselenoesters as Antiproliferative Agents.Molecules (Basel, Switzerland) · 2017
    Article
  10. Article
  11. Article
  12. Article
  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

8 authors at 3 institutions in 1 country.

Xiaojing WuThe Clinical Department, College of Veterinary Medicine, China Agricultural University, Beijing 100193, China.
Yidi Zhang
Zengyang Pei
Si Chen
Xu Yang
Yin Chen
Degui Lin
Runlin Z Ma
China Agricultural University · CNUniversity of Chinese Academy of Sciences · CNBeijing Sanbo Brain Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAngiopoietin-2 (Ang-2) plays critical roles in vascular morphogenesis and its upregulation is frequently associated with various tumors. Previous studies showed that certain selenium compounds possess anti-tumor effects. However, the underlining mechanism has not been elucidated in detail. Plus, results of research on the anti-tumor effects of selenium compounds remain controversial.

methodsWe investigated levels of Ang-2 and vascular endothelial growth factor (VEGF) on the estrogen-independent bone metastatic mammary cancer (MDA-MB-231) cells in response to treatment by methylseleninic acid (MSeA), and further examined the effects of MSeA oral administration on xenograft mammary tumors of athymic nude mice by RT-PCR, Western, radioimmuno assay, and Immunohistochemistry.

resultsTreatment of MDA-MB-231 cells with MSeA caused significant reduction of Ang-2 mRNA transcripts and secretion of Ang-2 proteins by the cells. Level of VEGF protein was accordingly decreased following the treatment. Compared with the controls, oral administration of MSeA (3 mg/kg/day for 18 days) to the nude mice carrying MDA-MB-231 induced tumors resulted in significant reduction in xenograft tumor volume and weights, significant decrease in microvascular density, and promotion of vascular normalization by increasing pericytes coverage. As expected, level of VEGF was also decreased in MSeA treated tumors.

conclusionsOur results point out that MSeA exerts its anti-tumor effects, at least in part, by inhibiting the Ang-2/Tie2 pathway, probably via inhibiting VEGF.

Indexed as

Xenograft Model Antitumor AssaysAngiopoietin-2AnimalsBlotting, WesternBone NeoplasmsBreast NeoplasmsCell Line, TumorFemaleGene ExpressionHumansImmunohistochemistryMiceMice, NudeOrganoselenium CompoundsReverse Transcriptase Polymerase Chain ReactionRNA InterferenceAngiopoietin-2methylselenic acidOrganoselenium CompoundsVascular Endothelial Growth Factor A

Identifiers

PMID22640261
PMCPMC3517305
OpenAlexW2019283626

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LicenceCC BY
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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.