Evidence map›Paper›PMID 18490922›Full record

ArticleOncogene2008

A 45-kDa ErbB3 secreted by prostate cancer cells promotes bone formation.

S-H Lin, C-J Cheng, Y-C Lee, X Ye, W-W Tsai, J Kim, R Pasqualini, W Arap, N M Navone, S-M Tu and 3 more

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

21 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Evaluation of Protein Levels of the Receptor Tyrosine Kinase ErbB3 in Serum.Methods in molecular biology (Clifton, N.J.) · 2018
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Bone matrix osteonectin limits prostate cancer cell growth and survival.Matrix biology : journal of the International Society for Matrix Biology · 2012
    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

13 authors at 4 institutions in 5 countries.

S-H LinDepartment of Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. slin@mdanderson.org
C-J Cheng
Y-C Lee
X Ye
W-W Tsai
J Kim
R Pasqualini
W Arap
N M Navone
S-M Tu
M Hu
L-Y Yu-Lee
C J Logothetis
The University of Texas MD Anderson Cancer Center · USBaylor College of Medicine · USSpanish Oncology Genitourinary Group · ESTaipei Medical University · TW

Funding

University of Texas SPORE in Prostate CancerP50CA090270 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LOGOTHETIS, CHRISTOPHER J. · 2001 to 2007
$13.6M
GENE SEQUENCES INVOLVED IN PROLACTIN ACTIONR01DK053176 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI YU-LEE, LI-YUAN · 1998 to 2007
$1.7M
Bone Metastasis Factor-1 in Prostate Cancer/Bone InteractionR01CA111479 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LIN, SUE-HWA · 2005 to 2009
$1.3M
NCI NIH HHS CA111479NCI NIH HHS P50 CA090270NCI NIH HHS P50-CA90270NCI NIH HHS R01 CA111479NIDDK NIH HHS DK53176NIDDK NIH HHS R01 DK053176
6 · The paper itself

Abstract

ErbB3 is a transmembrane growth factor receptor that has been implicated in the pathogenesis of human cancer. After finding that a truncated form of ErbB3 was present and upregulated in metastatic prostate cancer cells in lymph nodes and bone, we explored the pathophysiological functions of this unusual form of ErbB3 in the context of mouse calvaria as well as osteoblasts in vitro and the femur microenvironment in vivo. Here we demonstrate that prostate cancer cells expressed an alternatively spliced transcript that encodes a 45-kDa glycosylated protein (p45-sErbB3). The recombinant p45-sErbB3 purified from conditioned medium stimulated calvarial bone formation and induced osteoblast differentiation. Overexpression of p45-sErbB3 in the osteolytic prostate cancer cell line PC-3 converted its phenotype from bone lysing to bone forming upon injection into the femurs of immunodeficient mice. Further, we detected sErbB3 in plasma samples from patients with castration-resistant prostate cancer with bone metastasis. These observations establish that p45-sErbB3 is a structurally and functionally unique gene product of ErbB3 and suggest that p45-sErbB3 is likely one of the factors involved in the osteoblastic bone metastases of prostate cancer.

Indexed as

Alternative SplicingAnimalsBase SequenceBone DevelopmentBone NeoplasmsCell Line, TumorCulture Media, ConditionedDNA PrimersHumansMaleMiceOsteoblastsProstatic NeoplasmsReceptor, ErbB-3Reverse Transcriptase Polymerase Chain ReactionRNA, MessengerCulture Media, ConditionedDNA PrimersReceptor, ErbB-3RNA, Messenger

Identifiers

PMID18490922
PMCPMC2562662
OpenAlexW2091409116

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.