Evidence map›Paper›PMID 21266348›Full record

ArticleCancer research2011

HSulf-1 modulates FGF2- and hypoxia-mediated migration and invasion of breast cancer cells.

Ashwani Khurana, Peng Liu, Pasquale Mellone, Laura Lorenzon, Bruno Vincenzi, Kaustubh Datta, Bo Yang, Robert J Linhardt, Wilma Lingle, Jeremy Chien and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 11% 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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Bioinformatic Approach to Identify Positive PrognosticInternational journal of molecular sciences · 2025
    Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  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

12 authors at 4 institutions in 2 countries.

Ashwani KhuranaDepartment of Experimental Pathology, Mayo Clinic College of Medicine, Rochester, Minnesota 55905, USA.
Peng Liu
Pasquale Mellone
Laura Lorenzon
Bruno Vincenzi
Kaustubh Datta
Bo Yang
Robert J Linhardt
Wilma Lingle
Jeremy Chien
Alfonso Baldi
Viji Shridhar
Mayo Clinic · USUniversità Campus Bio-Medico · ITUniversity of Campania "Luigi Vanvitelli" · ITRensselaer Polytechnic Institute · US

Funding

Role of HSulf-1 Loss in Apoptosis and Drug ResistanceR01CA106954 · NCI · MAYO CLINIC ROCHESTER · PI SHRIDHAR, VIJI · 2004 to 2007
$949k
NCI NIH HHS R01 CA106954
6 · The paper itself

Abstract

HSulf-1 modulates the sulfation states of heparan sulfate proteoglycans critical for heparin binding growth factor signaling. In the present study, we show that HSulf-1 is transcriptionally deregulated under hypoxia in breast cancer cell lines. Knockdown of HIF-1α rescued HSulf-1 downregulation imposed by hypoxia, both at the RNA and protein levels. Chromatin immunoprecipitation with HIF-1α and HIF-2α antibodies confirmed recruitment of HIF-α proteins to the two functional hypoxia-responsive elements on the native HSulf-1 promoter. HSulf-1 depletion in breast cancer cells resulted in an increased and sustained bFGF2 (basic fibroblast growth factor) signaling and promoted cell migration and invasion under hypoxic conditions. In addition, FGFR2 (fibroblast growth factor receptor 2) depletion in HSulf-1-silenced breast cancer cells attenuated hypoxia-mediated cell invasion. Immunohistochemical analysis of 53 invasive ductal carcinomas and their autologous metastatic lesions revealed an inverse correlation for the expression of HSulf-1 to CAIX in both the primary tumors (P ≥ 0.0198) and metastatic lesions (P ≥ 0.0067), respectively, by χ(2) test. Finally, HSulf-1 expression levels in breast tumors by RNA in situ hybridization showed that high HSulf-1 expression is associated with increased disease-free and overall survival (P ≥ 0.03 and P ≥ 0.0001, respectively). Collectively, these results reveal an important link between loss of HSulf-1 under hypoxic microenvironment and increased growth factor signaling, cell migration, and invasion.

Indexed as

Cell MovementAdultAgedAged, 80 and overBasic Helix-Loop-Helix ProteinsBreast NeoplasmsCell HypoxiaCell Line, TumorEndothelial PAS Domain-Containing Protein 1FemaleFibroblast Growth Factor 2Gene Expression Regulation, NeoplasticHumansHypoxia-Inducible Factor 1, alpha SubunitImmunoblottingImmunohistochemistryBasic Helix-Loop-Helix ProteinsEndothelial PAS Domain-Containing Protein 1Fibroblast Growth Factor 2Hypoxia-Inducible Factor 1, alpha SubunitSULF1 protein, humanSulfotransferases

Identifiers

PMID21266348
PMCPMC3059381
OpenAlexW2121297515

What OpenQuestion holds

Textmetadata
LicenceTDM
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.