Evidence map›Paper›PMID 15750631›Full record

ArticleOncogene2005

Cell-autonomous induction of functional tumor suppressor 15-lipoxygenase 2 (15-LOX2) contributes to replicative senescence of human prostate progenitor cells.

Bobby Bhatia, Shaohua Tang, Peiying Yang, Andreas Doll, Gerhard Aumüeller, Robert A Newman, Dean G Tang

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Mammalian lipoxygenases and their biological relevance.Biochimica et biophysica acta · 2015
    Review
  9. Article
  10. Article
  11. Cyclooxygenases and lipoxygenases in cancer.Cancer metastasis reviews · 2011
    Review
  12. Article
  13. Article
  14. Review
  15. ALDH1A1 is a marker for malignant prostate stem cells and predictor of prostate cancer patients' outcome.Laboratory investigation; a journal of technical methods and pathology · 2010
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

7 authors at 2 institutions in 2 countries.

Bobby BhatiaDepartment of Carcinogenesis, The University of Texas MD Anderson Cancer Center, Science Park-Research Division, 1808 Park Rd. 1C, Smithville, TX 78957, USA.
Shaohua Tang
Peiying Yang
Andreas Doll
Gerhard Aumüeller
Robert A Newman
Dean G Tang
The University of Texas MD Anderson Cancer Center · USPhilipps University of Marburg · DE

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Pilot Project ProgramP30ES007784 · NIEHS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI RICHIE, ELLEN R · 1996 to 2011
$16.4M
TARGETING COX-2 AND EGFR SIGNALING IN ORAL CARCINOGENESISP01CA106451 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LIPPMAN, SCOTT M · 2004 to 2009
$8.3M
15-Lipoxygenase 2 is a Prostate Senescence GeneR01AG023374 · NIA · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI TANG, DEAN G. · 2004 to 2008
$1.4M
MITOCHONDRIA SIGNALED APOPTOSIS IN PROSTATE CANCER CELLSR01CA090297 · NCI · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI TANG, DEAN G · 2000 to 2004
$1.2M
NCI NIH HHS CA16672NCI NIH HHS CA90297NCI NIH HHS P01 CA106451NIA NIH HHS AG023374NIEHS NIH HHS P50 ES07784
6 · The paper itself

Abstract

Normal human prostatic (NHP) epithelial cells undergo senescence in vitro and in vivo, but little is known about the tissue-specific molecular mechanisms. Here we first characterize young primary NHP cells as CK5(+)/CK18(+) intermediate basal cells that also express several other putative stem/progenitor cell markers including p63, CD44, alpha2beta1, and hTERT. When cultured in serum- and androgen-free medium, NHP cells gradually lose the expression of these markers, slow down in proliferation, and enter senescence. Several pieces of evidence implicate 15-lipoxygenase 2 (15-LOX2), a molecule with a restricted tissue expression and most abundantly expressed in adult human prostate, in the replicative senescence of NHP cells. First, the 15-LOX2 promoter activity and the mRNA and protein levels of 15-LOX2 and its multiple splice variants are upregulated in serially passaged NHP cells, which precede replicative senescence and occur in a cell-autonomous manner. Second, all immortalized prostate epithelial cells and prostate cancer cells do not express 15-LOX2. Third, PCa cells stably transfected with 15-LOX2 or 15-LOX2sv-b, a splice variant that does not possess arachidonate-metabolizing activity, show a passage-related senescence-like phenotype. Fourth, infection of early-passage NHP cells with retroviral vectors encoding 15-LOX2 or 15-LOX2sv-b induces partial cell-cycle arrest and big and flat senescence-like phenotype. Finally, 15-LOX2 protein expression in human prostate correlates with age. Together, these data suggest that 15-LOX2 may represent an endogenous prostate senescence gene and its tumor-suppressing functions might be associated with its ability to induce cell senescence.

Indexed as

AdolescentAdultArachidonate 15-LipoxygenaseBiomarkers, TumorBlotting, WesternCellular SenescenceHumansMaleMiddle AgedProstateReverse Transcriptase Polymerase Chain ReactionStem CellsTranscriptional ActivationTumor Cells, CulturedUp-RegulationArachidonate 15-LipoxygenaseBiomarkers, Tumor

Identifiers

PMID15750631
OpenAlexW2036932424

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.