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Repression of M-phase phosphoprotein 8 inhibits melanoma growth and metastasis in vitro and in vivo.
Yuan, Bo; Lin, Lei; Ying, Zhen-Yi; Ying, Meng-Xia; Zhou, Qiong-Yan; Shi, Lei.
Afiliación
  • Yuan B; Department of Dermatology, The Affiliated Hospital of Medical School, Ningbo University Ningbo 315020, China.
  • Lin L; Department of Aesthetic Medicine, Ningbo College of Health Sciences Ningbo, China.
  • Ying ZY; Department of Dermatology, The Affiliated Hospital of Medical School, Ningbo University Ningbo 315020, China.
  • Ying MX; Department of Dermatology, The Affiliated Hospital of Medical School, Ningbo University Ningbo 315020, China.
  • Zhou QY; Department of Dermatology, The Affiliated Hospital of Medical School, Ningbo University Ningbo 315020, China.
  • Shi L; Department of Dermatology, The Affiliated Hospital of Medical School, Ningbo University Ningbo 315020, China.
Int J Clin Exp Pathol ; 10(12): 12003-12009, 2017.
Article en En | MEDLINE | ID: mdl-31966565
ABSTRACT
Metastatic melanoma accounts for the majority of skin cancer deaths due to its aggressiveness and high resistance to current therapies. M-phase phosphoprotein 8 (MPP8) has been shown to bind to methylated H3K9 and promote tumor cell motility and invasion. The current study aimed to investigate the role of MPP8 in melanoma growth and metastasis. Our results showed that MMP8 was up-regulated in the metastatic melanoma specimens. Knockdown of MPP8 inhibited melanoma cell growth both in vitro and in vivo. Furthermore, down-regulation of MPP8 induced S-phase cell cycle arrest as well as altered expression of cell cycle-related proteins in melanoma cells. In addition, repression of MPP8 inhibited the migration and invasion of melanoma cells both in vitro and in vivo. Taken together, these data suggest that MPP8 knockdown could inhibit the growth and metastasis of melanoma cells and provide novel therapeutic target for melanoma treatment.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Int J Clin Exp Pathol Asunto de la revista: PATOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Int J Clin Exp Pathol Asunto de la revista: PATOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: China