Evidence map›Paper›PMID 20166133›Full record

ArticleThe Prostate2010

Differential expression of the alpha2 chain of the interleukin-13 receptor in metastatic human prostate cancer ARCaPM cells.

Hui He, Jianchun Xu, Peter S Nelson, Fray F Marshall, Leland W K Chung, Haiyen E Zhau, Dalin He, Ruoxiang Wang

Abstract read
In one paragraph

Article in The Prostate, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.1field-weighted citation impact, top 46% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

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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

8 authors at 4 institutions in 2 countries.

Hui HeDepartment of Urology, the First Affiliated Hospital, Xi'an Jiaotong University, Xi'an, China.
Jianchun Xu
Peter S Nelson
Fray F Marshall
Leland W K Chung
Haiyen E Zhau
Dalin He
Ruoxiang Wang
Emory University · USCedars-Sinai Medical Center · USFirst Affiliated Hospital of Xi'an Jiaotong University · CNFred Hutch Cancer Center · US

Funding

Prostate Cancer Bone Metastasis: Biology and TargetingP01CA098912 · NCI · EMORY UNIVERSITY · PI ZAYZAFOON, MAJD · 2003 to 2019
$24.0M
Beta 2-Microglobulin signaling and targeting in bone metastasisR01CA122602 · NCI · CEDARS-SINAI MEDICAL CENTER · PI CHUNG, LELAND W.K. · 2009 to 2013
$1.5M
MSM/WCI Partnership To Investigate Mechanisms of Prostate Cancer: Planning StageP20CA132388 · NCI · EMORY UNIVERSITY · PI MARSHALL, FRAY F. · 2007 to 2009
$407k
Functional characterization of PrLZ in prostate cancerR21CA112330 · NCI · EMORY UNIVERSITY · PI WANG, RUOXIANG · 2005 to 2006
$260k
NCI NIH HHS CA132388NCI NIH HHS CA98912-02NCI NIH HHS P01 CA098912NCI NIH HHS P20 CA132388NCI NIH HHS PC040578NCI NIH HHS R01 CA122602NCI NIH HHS R21 CA112330NCI NIH HHS R21CA112330
6 · The paper itself

Abstract

backgroundThe alpha2 chain of the interleukin-13 receptor (IL13Ralpha2) is a high-affinity receptor and a candidate target for cytotoxic killing of cancer cells. Availability of a human prostate cancer cell line with high level of IL13Ralpha2 expression will facilitate the development of therapeutic modalities.

methodsARCaP(E) and ARCaP(M) human prostate cancer cell lines were subjected to comparative analyses of gene expression. Expression of the IL13Ralpha2 protein was confirmed by Western blotting and immunostaining. IL13Ralpha2 proteins in xenograft tumors and clinical human prostate cancer specimens were detected by specific antibodies. LNCaP prostate cancer cells stably transfected with IL13Ralpha2 were examined for accelerated growth in athymic mice.

resultsWe found that IL13Ralpha2 proteins could be detected in both the ARCaP(E) and ARCaP(M) cells, but the expression level in ARCaP(M) was more than 17-fold higher than in ARCaP(E) cells. Importantly, the ARCaP lineage represented the only human prostate cancer cell line that expresses IL13Ralpha2 proteins at the level detectable by Western blotting. Expression of IL13Ralpha2 was accompanied by resistance to the anti-tumor activity of interleukin-13 (IL-13). ARCaP cells were found to be insensitive to growth inhibition upon IL-13 treatment, while overexpression of IL13Ralpha2 in LNCaP cells promoted intratibial tumor growth in athymic mice.

conclusionsDifferential IL13Ralpha2 expression may account for the high tumorigenic and metastatic potential of ARCaP(M) cells. The unique expression of IL13Ralpha2 makes ARCaP lineage an attractive model for evaluating the targeting efficacy of therapeutic agents based on IL13Ralpha2 protein expression.

Indexed as

AnimalsBlotting, WesternCell Line, TumorCell ProliferationCells, CulturedGene Expression Regulation, NeoplasticHumansImmunohistochemistryInterleukin-13Interleukin-13 Receptor alpha2 SubunitMaleMiceMice, NudeProstateReverse Transcriptase Polymerase Chain ReactionTransfectionInterleukin-13Interleukin-13 Receptor alpha2 Subunit

Identifiers

PMID20166133
PMCPMC3180892
OpenAlexW2147038619

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.