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LncRNA PITPNA-AS1 mediates the diagnostic potential of miR-129-5p in prostate cancer.
Song, Zhaolu; Xu, Silei; Gu, Xiaohui; Feng, Qiang; Wang, Chang.
Afiliación
  • Song Z; Department of Urology Surgery, Jiaozhou Central Hospital of Qingdao, Shandong, 266300, China.
  • Xu S; Medical School of University of Electronic Science and Technology of China, Chengdu, 610051, China.
  • Gu X; Department of Urinary Surgery, Sichuan Academy of Medical Sciences, Sichuan Provincial People's Hospital, No. 32, West Section 2, 1st Ring Road, Qingyang District, Chengdu, 610031, China.
  • Feng Q; Department of Urinary Surgery, Sichuan Academy of Medical Sciences, Sichuan Provincial People's Hospital, No. 32, West Section 2, 1st Ring Road, Qingyang District, Chengdu, 610031, China. fengqiangdr@163.com.
  • Wang C; Organ Transplant Center, The First Affiliated Hospital, Sun Yat-sen University, No. 58, Zhongshan Second Road, Guangzhou City, 510080, Guangdong Province, China. Wangchanggz@163.com.
BMC Urol ; 24(1): 146, 2024 Jul 13.
Article en En | MEDLINE | ID: mdl-39003446
ABSTRACT

BACKGROUND:

LncRNA has an effective value in many diseases, which has long been applied in the diagnosis, treatment and prognosis of prostate cancer. This study focused on lncRNA PITPNA-AS1, and its diagnostic potential in prostate cancer has been explored.

METHODS:

The expression of PITPNA-AS1 and miR-129-5p in prostate cancer serum and sample cells was determined by real-time quantitative polymerase chain reaction (RT-qPCR). The relationship between the expression of PITPNA-AS1 and clinicopathological parameters was considered. ROC curve prompted the diagnostic value of PITPNA-AS1. The effect of PITPNA-AS1 on prostate cancer cells was verified using vitro cells assay. Luciferase activity assay and RIP assay demonstrated the sponge relationship of PITPNA-AS1 to miR-129-5p.

RESULTS:

PITPNA-AS1 level was increased, while miR-129-5p was obviously decreased in prostate cancer. PITPNA-AS1 expression was associated with Gleason grade, lymph node metastasis and TNM stage in patients. The area under the curve (AUC) was 0.910, with high sensitivity and specificity. PITPNA-AS1 was elucidated to directly target miR-129-5p, whereas silencing PITPNA-AS1 negatively affected prostate cancer cell proliferation, migration and invasion. Intervention of miR-129-5p inhibitor reversed the effect of silencing PITPNA-AS1 on cells.

CONCLUSIONS:

PITPNA-AS1 was relatively highly expressed in prostate cancer and mediated the pathophysiological process of patients, which may serve as a diagnostic indicator. Silencing of the PITPNA-AS1 sponge miR-129-5p inhibited the biological function of the cells, indicating that PITPNA-AS1 may represent a novel therapeutic target for prostate cancer.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / MicroARNs / ARN Largo no Codificante Límite: Aged / Humans / Male / Middle aged Idioma: En Revista: BMC Urol Asunto de la revista: UROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / MicroARNs / ARN Largo no Codificante Límite: Aged / Humans / Male / Middle aged Idioma: En Revista: BMC Urol Asunto de la revista: UROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: China