2. Academic Validation
  3. The role of AFAP1-AS1 in mitotic catastrophe and metastasis of triple-negative breast cancer cells by activating the PLK1 signaling pathway

The role of AFAP1-AS1 in mitotic catastrophe and metastasis of triple-negative breast cancer cells by activating the PLK1 signaling pathway

  • Oncol Res. 2023 May 24;31(3):375-388. doi: 10.32604/or.2023.028256.
Shuizhong Cen 1,  Xiaojie Peng 2,  Jianwen Deng 3,  Haiyun Jin 4,  Zhinan Deng 5,  Xiaohua Lin 3,  D I Zhu 3,  Ming Jin 6,  Yanwen Zhu 3,  Pusheng Zhang 3,  Yunfeng Luo 3,  Hongyan Huang 3
Affiliations

Affiliations

  • 1 Department of Spinal Surgery, Orthopedic Medical Center, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, China.
  • 2 Department of Critical Care Medicine, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China.
  • 3 Department of Breast Surgery, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, China.
  • 4 Department of Gynecology and Obstetrics, Southern Hospital Taihe Branch, Southern Medical University, Guangzhou, 510540, China.
  • 5 Department of Clinical Medicine, Nanshan Class, Guangzhou Medical University, Guangzhou, 511436, China.
  • 6 Department of Gastroenterology, Shenzhen Hospital, Southern Medical University, Shenzhen, 518110, China.
PMID: 37305386 DOI: 10.32604/or.2023.028256
Abstract

Triple-negative breast Cancer (TNBC) is characterized by fast growth, high metastasis, high invasion, and a lack of therapeutic targets. Mitosis and metastasis of TNBC cells are two important biological behaviors in TNBC malignant progression. It is well known that the long noncoding RNA AFAP1-AS1 plays a crucial role in various tumors, but whether AFAP1-AS1 is involved in the mitosis of TNBC cells remains unknown. In this study, we investigated the functional mechanism of AFAP1-AS1 in targeting Polo-like Kinase 1 (PLK1) activation and participating in mitosis of TNBC cells. We detected the expression of AFAP1-AS1 in the TNBC patient cohort and primary cells by in situ hybridization (ISH), northern blot, fluorescent in situ hybridization (FISH) and cell nucleus/cytoplasm RNA fraction isolation. High AFAP1-AS1 expression was negatively correlated with overall survival (OS), disease-free survival (DFS), metastasis-free survival (MFS) and recurrence-free survival (RFS) in TNBC patients. We explored the function of AFAP1-AS1 by transwell, Apoptosis, immunofluorescence (IF) and patient-derived xenograft (PDX) models in vitro and in vivo. We found that AFAP1-AS1 promoted TNBC primary cell survival by inhibiting mitotic catastrophe and increased TNBC primary cell growth, migration and invasion. Mechanistically, AFAP1-AS1 activated phosphorylation of the mitosis-associated kinase PLK1 protein. Elevated levels of AFAP1-AS1 in TNBC primary cells increased PLK1 pathway downstream gene expression, such as CDC25C, CDK1, BUB1 and TTK. More importantly, AFAP1-AS1 increased lung metastases in a mouse metastasis model. Taken together, AFAP1-AS1 functions as an oncogene that activates the PLK1 signaling pathway. AFAP1-AS1 could be used as a potential prognostic marker and therapeutic target for TNBC.

Keywords

AFAP1-AS1; Metastasis; Mitotic catastrophe; PLK1; TNBC.

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