Comparison of ERG and SPINK1 expression among incidental and metastatic prostate cancer in Japanese men.


Journal

The Prostate
ISSN: 1097-0045
Titre abrégé: Prostate
Pays: United States
ID NLM: 8101368

Informations de publication

Date de publication:
01 2019
Historique:
received: 19 03 2018
accepted: 13 07 2018
pubmed: 28 7 2018
medline: 12 4 2019
entrez: 28 7 2018
Statut: ppublish

Résumé

TMPRSS2:ERG fusion is the most common genetic event in prostate cancer (PCa). However, its association with prognosis is controversial. Overexpression of serine protease inhibitor Kazal-type 1 (SPINK1) was almost exclusively defined in ERG-negative PCa in most studies. This study aimed to determine the association between ERG and SPINK1 expression and the biological aggressiveness of PCa by analyzing their expression in incidental and metastatic cohorts. A total of 143 cystoprostatectomy specimens of invasive bladder cancer and 98 biopsy specimens from de novo metastatic PCa were analyzed. The prostate gland of cystoprostatectomy specimens was fixed and sliced in step sections. Immunohistochemistry of ERG and SPINK1 was conducted, and the results were correlated with the clinicopathological characteristics of the patients. The overall prevalence of incidental cancer was 32.2% (46/143). The frequencies of both ERG and SPINK1 expression were not significantly different between incidental and metastatic cohorts (15.2% and 14.3%; P = 1.00, and 6.5% and 12.2%; P = 0.38, respectively). In the metastatic cohort, any pre-treatment factors were not significantly associated with the frequencies of ERG and SPINK1 expression. However, SPINK1 expression was significantly associated with a shorter time to castration-resistant PCa (CRPC) (P = 0.048). Meanwhile, overall survival was not significantly associated with the expression status of ERG and SPINK1 (P = 0.71). ERG and SPINK1 expression may not have significant influence on the metastatic behavior of PCa. SPINK1 expression was significantly associated with a shorter time to CRPC in metastatic PCa. The expression profile of ERG and SPINK1 may be a useful predictor for effect of androgen deprivation therapy in patients with metastatic castration-sensitive PCa.

Sections du résumé

BACKGROUND
TMPRSS2:ERG fusion is the most common genetic event in prostate cancer (PCa). However, its association with prognosis is controversial. Overexpression of serine protease inhibitor Kazal-type 1 (SPINK1) was almost exclusively defined in ERG-negative PCa in most studies. This study aimed to determine the association between ERG and SPINK1 expression and the biological aggressiveness of PCa by analyzing their expression in incidental and metastatic cohorts.
METHODS
A total of 143 cystoprostatectomy specimens of invasive bladder cancer and 98 biopsy specimens from de novo metastatic PCa were analyzed. The prostate gland of cystoprostatectomy specimens was fixed and sliced in step sections. Immunohistochemistry of ERG and SPINK1 was conducted, and the results were correlated with the clinicopathological characteristics of the patients.
RESULTS
The overall prevalence of incidental cancer was 32.2% (46/143). The frequencies of both ERG and SPINK1 expression were not significantly different between incidental and metastatic cohorts (15.2% and 14.3%; P = 1.00, and 6.5% and 12.2%; P = 0.38, respectively). In the metastatic cohort, any pre-treatment factors were not significantly associated with the frequencies of ERG and SPINK1 expression. However, SPINK1 expression was significantly associated with a shorter time to castration-resistant PCa (CRPC) (P = 0.048). Meanwhile, overall survival was not significantly associated with the expression status of ERG and SPINK1 (P = 0.71).
CONCLUSIONS
ERG and SPINK1 expression may not have significant influence on the metastatic behavior of PCa. SPINK1 expression was significantly associated with a shorter time to CRPC in metastatic PCa. The expression profile of ERG and SPINK1 may be a useful predictor for effect of androgen deprivation therapy in patients with metastatic castration-sensitive PCa.

Identifiants

pubmed: 30051483
doi: 10.1002/pros.23705
doi:

Substances chimiques

Biomarkers, Tumor 0
ERG protein, human 0
SPINK1 protein, human 0
Transcriptional Regulator ERG 0
Trypsin Inhibitor, Kazal Pancreatic 50936-63-5

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3-8

Informations de copyright

© 2018 Wiley Periodicals, Inc.

Auteurs

Haruhisa Koide (H)

Department of Urology, Jikei University School of Medicine, Tokyo, Japan.

Takahiro Kimura (T)

Department of Urology, Jikei University School of Medicine, Tokyo, Japan.

Hiroyuki Inaba (H)

Department of Urology, Jikei University School of Medicine, Tokyo, Japan.

Shun Sato (S)

Department of Pathology, Jikei University School of Medicine, Tokyo, Japan.

Kosuke Iwatani (K)

Department of Urology, Jikei University School of Medicine, Tokyo, Japan.

Takashi Yorozu (T)

Department of Pathology, Jikei University School of Medicine, Tokyo, Japan.

Bungo Furusato (B)

Department of Pathology, Jikei University School of Medicine, Tokyo, Japan.
Department of Pathology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

Yuko Kamata (Y)

Division of Oncology, Jikei University School of Medicine, Tokyo, Japan.

Jun Miki (J)

Department of Urology, Jikei University School of Medicine, Tokyo, Japan.

Hiroshi Kiyota (H)

Department of Urology, Jikei University School of Medicine, Tokyo, Japan.

Hiroyuki Takahashi (H)

Department of Pathology, Jikei University School of Medicine, Tokyo, Japan.

Shin Egawa (S)

Department of Urology, Jikei University School of Medicine, Tokyo, Japan.

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