Evidence map›Paper›PMID 18266970›Full record

ArticleJournal of cellular and molecular medicine2008

Down-regulation of osteopontin attenuates breast tumour progression in vivo.

Goutam Chakraborty, Shalini Jain, Tushar V Patil, Gopal C Kundu

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. New Insights into LINC00346 and its Role in Disease.Frontiers in cell and developmental biology · 2021
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Pre- and post-translational regulation of osteopontin in cancer.Journal of cell communication and signaling · 2011
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Adenosine and osteopontin contribute to the development of chronic obstructive pulmonary disease.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2010
    Article
  17. Osteopontin and oral carcinogenesis.Journal of cellular and molecular medicine · 2008
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Goutam ChakrabortyNational Center for Cell Science, Department of Histopathology, YCM Hospital, Pune, India.
Shalini Jain
Tushar V Patil
Gopal C Kundu
National Centre for Cell Science · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Development of breast tumour malignancies results in enhanced expression of various oncogenic molecules. Elevated expression of osteopontin (OPN) in higher grades of breast carcinoma correlates with enhanced expressions of several oncogenic molecules (urokinase-type plasminogen activator [uPA], matrix metalloproteinase-2/-9 [MMP-2 and -9]) and increased angiogenic potential of breast carcinoma. In this study, using in vitro and multiple in vivo models, we have demonstrated that silencing of OPN by its specific small interfering RNA (siRNA) down-regulates the expressions of oncogenic molecules such as uPA, MMP-2 and -9 resulting in inhibition of in vitro cell motility and in vivo tumourigenicity in mice. Moreover our results demonstrated that OPN-/- mice showed slower progression of tumour growth in breast cancer model as compared to wild-type mice. Furthermore, the data showed that injection of carcinogenic compound, pristane (2, 6,10,14-tetramethylpen-tadecane) induces breast tumour progression leading to enhanced expression of OPN and other oncogenic molecules in mammary fat pad of nude- and wild-type mice but not in OPN-/- mice. However, intratumoural injection of OPN siRNA to pristane-induced tumour significantly suppressed these effects. Our data revealed that knocking down of OPN effectively curb breast cancer progression and further suggested that developing of OPN-based therapeutics might be an emerging approach for the next generation of breast cancer management.

Indexed as

AnimalsBase SequenceBreast NeoplasmsCell Line, TumorCell MovementDown-RegulationFemaleHumansMammary Neoplasms, ExperimentalMatrix MetalloproteinasesMiceMice, Inbred C57BLMice, KnockoutMice, NudeNeoplasm TransplantationNeovascularization, PathologicMatrix MetalloproteinasesNF-kappa BOsteopontinpristaneRNA, Small InterferingSpp1 protein, mouseTerpenesUrokinase-Type Plasminogen Activatorvon Willebrand Factor

Identifiers

PMID18266970
PMCPMC4514110
OpenAlexW2122056974

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.