Evidence map›Paper›PMID 36806727›Full record

ArticleCancer reports (Hoboken, N.J.)2023

Identification of the α2 chain of interleukin-13 receptor as a potential biomarker for predicting castration resistance of prostate cancer using patient-derived xenograft models.

Takahiro Nagai, Naoki Terada, Masato Fujii, Yasuhisa Nagata, Kozue Nakahara, Shoichiro Mukai, Kosuke Okasho, Yuki Kamiyama, Shusuke Akamatsu, Takashi Kobayashi and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 49% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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  3. Review
  4. 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

16 authors at 3 institutions in 1 country.

Takahiro NagaiDepartment of Urology, Miyazaki University Graduate School of Medicine, Miyazaki, Japan.ORCID 0000-0001-8427-644X
Naoki TeradaDepartment of Urology, Miyazaki University Graduate School of Medicine, Miyazaki, Japan.
Masato FujiiDepartment of Urology, Miyazaki University Graduate School of Medicine, Miyazaki, Japan.
Yasuhisa NagataDepartment of Urology, Miyazaki University Graduate School of Medicine, Miyazaki, Japan.
Kozue NakaharaDepartment of Urology, Miyazaki University Graduate School of Medicine, Miyazaki, Japan.
Shoichiro MukaiDepartment of Urology, Miyazaki University Graduate School of Medicine, Miyazaki, Japan.
Kosuke OkashoDepartment of Urology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Yuki KamiyamaDepartment of Urology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Shusuke AkamatsuDepartment of Urology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Takashi KobayashiDepartment of Urology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Kei IidaMedical Research Support Center, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Masatsugu DenawaMedical Research Support Center, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID 0000-0001-5808-8197
Masatoshi HagiwaraDepartment of Anatomy and Developmental Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Takahiro InoueDepartment of Nephro-Urologic Surgery and Andrology, Mie University Graduate School of Medicine, Tsu, Japan.
Osamu OgawaDepartment of Urology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Toshiyuki KamotoDepartment of Urology, Miyazaki University Graduate School of Medicine, Miyazaki, Japan.
Kyoto University · JPUniversity of Miyazaki · JPMie University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSeveral treatment strategies use upfront chemotherapy or androgen receptor axis-targeting therapies for metastatic prostate cancer. However, there are no useful biomarkers for selecting appropriate patients who urgently require these treatments.

methodsNovel patient-derived xenograft (PDX) castration-sensitive and -resistant models were established and gene expression patterns were comprehensively compared. The function of a gene highly expressed in the castration-resistant models was evaluated by its overexpression in LNCaP prostate cancer cells. Protein expression in the tumors and serum of patients was examined by immunohistochemistry and ELISA, and correlations with castration resistance were analyzed.

resultsExpression of the α2 chain of interleukin-13 receptor (IL13Rα2) was higher in castration-resistant PDX tumors. LNCaP cells overexpressing IL13Rα2 acquired castration resistance in vitro and in vivo. In tissue samples, IL13Rα2 expression levels were significantly associated with castration-resistant progression (p < 0.05). In serum samples, IL13Rα2 levels could be measured in 5 of 28 (18%) castration-resistant prostate cancer patients.

conclusionIL13Rα2 was highly expressed in castration-resistant prostate cancer PDX models and was associated with the castration resistance of prostate cancer cells. It might be a potential tissue and serum biomarker for predicting castration resistance in prostate cancer patients.

Indexed as

Interleukin-13 Receptor alpha2 SubunitProstatic Neoplasms, Castration-ResistantBiomarkersHeterograftsHumansMaleOrchiectomyBiomarkersInterleukin-13 Receptor alpha2 Subunitbiomarkercastration resistanceInterleukin-13 receptor α2patient-derived xenograftprostate cancer

Identifiers

PMID36806727
PMCPMC9939991
OpenAlexW4292448927

What OpenQuestion holds

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Registered trials

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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.