Evidence map›Paper›PMID 23322198›Full record

ArticleBritish journal of cancer2013

Cox-2 inhibition enhances the activity of sunitinib in human renal cell carcinoma xenografts.

X Wang, L Zhang, A O'Neill, B Bahamon, D C Alsop, J W Mier, S N Goldberg, S Signoretti, M B Atkins, C G Wood and 1 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

24 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Lipids as Targets for Renal Cell Carcinoma Therapy.International journal of molecular sciences · 2023
    Review
  5. Article
  6. Article
  7. Article
  8. Selenium and selenoproteins in prostanoid metabolism and immunity.Critical reviews in biochemistry and molecular biology · 2019
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Anti-S1P Antibody as a Novel Therapeutic Strategy for VEGFR TKI-Resistant Renal Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2015
    Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 2 countries.

X WangDepartment of Radiology, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Avenue, Boston, MA 02215, USA.
L Zhang
A O'Neill
B Bahamon
D C Alsop
J W Mier
S N Goldberg
S Signoretti
M B Atkins
C G Wood
R S Bhatt
Harvard University · USBeth Israel Deaconess Medical Center · USBrigham and Women's Hospital · USDana-Farber Cancer Institute · USGeorgetown Lombardi Comprehensive Cancer CenterThe University of Texas MD Anderson Cancer Center · US

Funding

Treating the P13-Kinase/AKTP50CA101942 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI Wanling Xie · 2003 to 2026
$53.4M
Mechanism of Acquired Resistance to VEGF-R Antagonists in RCCK08CA138900 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BHATT, RUPAL S · 2010 to 2014
$848k
NCI NIH HHS K08 CA138900NCI NIH HHS P50 CA101942NCI NIH HHS P50CA101942
6 · The paper itself

Abstract

backgroundSunitinib (Su), a tyrosine kinase inhibitor of VEGFR, is effective at producing tumour response in clear cell renal cell carcinoma (cRCC), but resistance to therapy is inevitable. As COX-2 is a known mediator of tumour growth, we explored the potential benefit of COX-2 inhibition in combination with VEGFR inhibition in attempts at delaying tumour progression on Su.

methodsCOX-2 expression was compared with areas of hypoxia in tumours that progressed on Su vs untreated tumours. Mice bearing human cRCC xenografts were treated with Su and the COX-2 inhibitor, celecoxib, and the effects on tumour growth were assessed. Sequential vs concurrent regimens were compared.

resultsCOX-2 expression was increased in cRCC xenografts in areas of tumour hypoxia. The combination of Su and celecoxib achieved longer times to tumour progression compared to treatment with either agent alone or to untreated control animals in four models. This effect was seen with concurrent but not with sequential therapy.

conclusionCOX-2 inhibition can extend the effectiveness of VEGFR inhibition. This effect is dependent on the timing of therapy. Clinical trials combining Su and COX-2 inhibitors should be considered as a means delaying time to progression on sunitinib in patients with metastatic cRCC.

Indexed as

Angiogenesis InhibitorsAnimalsAntineoplastic AgentsCarcinoma, Renal CellCelecoxibCell Line, TumorCell ProliferationCyclooxygenase 2Cyclooxygenase 2 InhibitorsFemaleHumansIndolesKidney NeoplasmsMicePyrazolesPyrrolesAngiogenesis InhibitorsAntineoplastic AgentsCelecoxibCyclooxygenase 2Cyclooxygenase 2 InhibitorsIndolesPTGS2 protein, humanPyrazolesPyrrolesReceptors, Vascular Endothelial Growth FactorSulfonamidesSunitinib

Identifiers

PMID23322198
PMCPMC3566808
OpenAlexW2029068983

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.