ARHGAP29 expression may be a novel prognostic factor of cell proliferation and invasion in prostate cancer.


Journal

Oncology reports
ISSN: 1791-2431
Titre abrégé: Oncol Rep
Pays: Greece
ID NLM: 9422756

Informations de publication

Date de publication:
12 2020
Historique:
received: 15 07 2019
accepted: 23 06 2020
pubmed: 31 10 2020
medline: 3 8 2021
entrez: 30 10 2020
Statut: ppublish

Résumé

Yes‑associated protein (YAP) is a transcription‑coupling factor that plays a central role in the Hippo pathway, and its activation regulates cell proliferation and carcinogenesis. YAP activation has been reported in various malignancies, conferring tumors with migratory and invasive abilities. Several studies have suggested that YAP expression is closely associated with prostate cancer. Furthermore, YAP has been revealed to regulate destabilization of F‑actin associated with the cytoskeleton via Rho GTPase‑activating protein 29 (ARHGAP29), suggesting that ARHGAP29 is associated with cancer metastasis. In the present study, the functions of ARHGAP29 were examined in four prostate cancer cell lines (22Rv1, LNCaP, DU145 and PC‑3) and it was revealed that upregulation of ARHGAP29 in LNCaP and DU145 cells with the lowest expression of ARHGAP29 promoted cell proliferation and invasion. Conversely, ARHGAP29 knockdown in PC‑3 cells with its highest expression level significantly reduced cell proliferation and invasion. In addition, immunohistochemistry of specimens from 133 patients who underwent radical prostatectomy was performed to investigate the clinical association between ARHGAP29 expression and prognosis in prostate cancer patients. Multivariate analysis demonstrated that ARHGAP29 was an independent prognostic factor for biochemical progression‑free survival (P=0.0123). These findings indicated that ARHGAP29 in prostate cancer may be a potential prognostic biomarker and therapeutic target.

Identifiants

pubmed: 33125156
doi: 10.3892/or.2020.7811
doi:

Substances chimiques

ARHGAP29 protein, human 0
Biomarkers, Tumor 0
GTPase-Activating Proteins 0

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

2735-2745

Auteurs

Kosuke Shimizu (K)

Department of Urology, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi 755-8505, Japan.

Hiroaki Matsumoto (H)

Department of Urology, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi 755-8505, Japan.

Hiroshi Hirata (H)

Department of Urology, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi 755-8505, Japan.

Koji Ueno (K)

Center for Regenerative Medicine, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi 755-8505, Japan.

Masahiro Samoto (M)

Department of Urology, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi 755-8505, Japan.

Junichi Mori (J)

Department of Urology, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi 755-8505, Japan.

Nakanori Fujii (N)

Department of Urology, Japan Community Health Care Organization Tokuyama Central Hospital, Shunan, Yamaguchi 745-8522, Japan.

Yoshihisa Kawai (Y)

Kawai Urological Clinic, Hofu, Yamaguchi 747-0836, Japan.

Ryo Inoue (R)

Department of Urology, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi 755-8505, Japan.

Yoshiaki Yamamoto (Y)

Department of Urology, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi 755-8505, Japan.

Seiji Yano (S)

Department of Urology, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi 755-8505, Japan.

Tomoyuki Shimabukuro (T)

Department of Urology, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi 755-8505, Japan.

Makoto Furutani-Seiki (M)

Department of Systems Biochemistry in Pathology and Regeneration, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi 755-8505, Japan.

Hideyasu Matsuyama (H)

Department of Urology, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi 755-8505, Japan.

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Classifications MeSH