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ADAM9 Mediates Triple-Negative Breast Cancer Progression via AKT/NF-κB Pathway.
Zhou, Rui; Cho, William C S; Ma, Victor; Cheuk, Wah; So, Yik-Ka; Wong, S C Cesar; Zhang, Mingrong; Li, Cong; Sun, Yujie; Zhang, Hong; Chan, Lawrence W C; Tian, Mei.
Afiliación
  • Zhou R; Department of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China.
  • Cho WCS; Department of Nuclear Medicine and Medical PET Center, The Second Hospital of Zhejiang University School of Medicine, Hangzhou, China.
  • Ma V; Department of Clinical Oncology, Queen Elizabeth Hospital, Hong Kong, China.
  • Cheuk W; Department of Clinical Oncology, Queen Elizabeth Hospital, Hong Kong, China.
  • So YK; Department of Pathology, Queen Elizabeth Hospital, Hong Kong, China.
  • Wong SCC; Department of Pathology, Queen Elizabeth Hospital, Hong Kong, China.
  • Zhang M; Department of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China.
  • Li C; Department of Advanced Nuclear Medicine Sciences, National Institute of Radiological Sciences, Chiba, Japan.
  • Sun Y; Key Laboratory of Smart Drug Delivery, Ministry of Education, School of Pharmacy, Fudan University, Shanghai, China.
  • Zhang H; State Key Laboratory of Membrane Biology, Biomedical Pioneer Innovation Center, School of Life Sciences, Peking University, Beijing, China.
  • Chan LWC; Department of Nuclear Medicine and Medical PET Center, The Second Hospital of Zhejiang University School of Medicine, Hangzhou, China.
  • Tian M; Key Laboratory for Biomedical Engineering of Ministry of Education, Zhejiang University, Hangzhou, China.
Front Med (Lausanne) ; 7: 214, 2020.
Article en En | MEDLINE | ID: mdl-32637415
ABSTRACT
Upregulation of a disintegrin and metalloprotease 9 (ADAM9) is correlated with progression of cancers, such as prostate, bladder, and pancreatic cancers. However, its role in triple-negative breast cancer (TNBC) is still unclear. Our study aimed to investigate whether ADAM9 is upregulated and promoted the aggressiveness in TNBC. Breast cancer cell lines and patient specimens were used to evaluate the ADAM9 expression by western blotting and immunohistochemistry staining, respectively. Compared with the non-TNBC, ADAM9 expression was significantly increased in TNBC cells and TNBC patient specimens. Based on the data acquired from public databases, the correlation between ADAM9 expression and breast cancer patient survival was analyzed by Kaplan-Meier method. It was shown that ADAM9 overexpression was significantly correlated with poorer survival in patients with TNBC. Furthermore, ADAM9 in TNBC cells was knocked down by small interference RNA and then studied by the MTT/colony formation assay, wound healing assay and transwell invasion assay on the cell proliferation, migration, and invasion, respectively. We found that inhibiting ADAM9 expression suppressed TNBC cell proliferation, migration, and invasion by lowering the activation of AKT/NF-κB pathway. Our results demonstrated that ADAM9 is an important molecule in mediating TNBC aggressiveness and may be a potential useful therapeutic target in TNBC treatment.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Front Med (Lausanne) Año: 2020 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Front Med (Lausanne) Año: 2020 Tipo del documento: Article País de afiliación: China