Evidence map›Paper›PMID 25859560›Full record

ArticleOncoscience2015

Versican is a potential therapeutic target in docetaxel-resistant prostate cancer.

Naoko Arichi, Yozo Mitsui, Miho Hiraki, Sigenobu Nakamura, Takeo Hiraoka, Masahiro Sumura, Hiroshi Hirata, Yuichiro Tanaka, Rajvir Dahiya, Hiroaki Yasumoto and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncoscience, 2015. 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 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

14 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Versican: A Dynamic Regulator of the Extracellular Matrix.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2020
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Cancer and the metastatic substrate.Ecancermedicalscience · 2016
    Review
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

11 authors at 3 institutions in 2 countries.

Naoko ArichiDepartments of Urology, Shimane University Faculty of Medicine, Izumo, Japan.
Yozo MitsuiDepartments of Urology, Shimane University Faculty of Medicine, Izumo, Japan ; Department of Urology, San Francisco Veterans Affairs Medical Center and University of California San Francisco, San Francisco, California.
Miho HirakiDepartments of Urology, Shimane University Faculty of Medicine, Izumo, Japan.
Sigenobu NakamuraDepartments of Urology, Shimane University Faculty of Medicine, Izumo, Japan.
Takeo HiraokaDepartments of Urology, Shimane University Faculty of Medicine, Izumo, Japan.
Masahiro SumuraDepartments of Urology, Shimane University Faculty of Medicine, Izumo, Japan.
Hiroshi HirataDepartment of Urology, San Francisco Veterans Affairs Medical Center and University of California San Francisco, San Francisco, California.
Yuichiro TanakaDepartment of Urology, San Francisco Veterans Affairs Medical Center and University of California San Francisco, San Francisco, California.
Rajvir DahiyaDepartment of Urology, San Francisco Veterans Affairs Medical Center and University of California San Francisco, San Francisco, California.
Hiroaki YasumotoDepartments of Urology, Shimane University Faculty of Medicine, Izumo, Japan.
Hiroaki ShiinaDepartments of Urology, Shimane University Faculty of Medicine, Izumo, Japan.
Shimane University · JPSan Francisco VA Medical Center · USUniversity of California, San Francisco · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the current study, we investigated a combination of docetaxel and thalidomide (DT therapy) in castration-resistant prostate cancer (CRPC) patients. We identified marker genes that predict the effect of DT therapy. Using an androgen-insensitive PC3 cell line, we established a docetaxel-resistant PC-3 cell line (DR-PC3). In DR-PC3 cells, DT therapy stronger inhibited proliferation/viability than docetaxel alone. Based on gene ontology analysis, we found versican as a selective gene. This result with the findings of cDNA microarray and validated by quantitative RT-PCR. In addition, the effect of DT therapy on cell viability was the same as the effect of docetaxel plus versican siRNA. In other words, silencing of versican can substitute for thalidomide. In the clinical setting, versican expression in prostate biopsy samples (before DT therapy) correlated with PSA reduction after DT therapy (p<0.05). Thus targeting versican is a potential therapeutic strategy in docetaxel-resistant prostate cancer.

Indexed as

castration resistant prostate cancertaxane resistancethalidomide chemotherapyversican

Identifiers

PMID25859560
PMCPMC4381710
OpenAlexW2097268059

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.