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LINC01234 promotes multiple myeloma progression by regulating miR-124-3p/GRB2 axis.
Chen, Xueyan; Liu, Yin; Yang, Zihua; Zhang, Jiang; Chen, Shaoqian; Cheng, Jing.
Afiliação
  • Chen X; Department of Clinical Laboratory, The People's Hospital of Longhua Shenzhen 518109, Guangdong Province, China.
  • Liu Y; Department of Laboratory Medicine, The First Affiliated Hospital of Sun Yat-sen University Guangzhou 510080, Guangdong Province, China.
  • Yang Z; Department of Clinical Laboratory, Shenzhen People's Hospital, 2nd Clinical Medical College of Jinan University Shenzhen 518020, Guangdong Province, China.
  • Zhang J; Department of Laboratory Medicine, The First Affiliated Hospital of Sun Yat-sen University Guangzhou 510080, Guangdong Province, China.
  • Chen S; Department of Laboratory Medicine, The First Affiliated Hospital of Sun Yat-sen University Guangzhou 510080, Guangdong Province, China.
  • Cheng J; Department of Laboratory Medicine, The First Affiliated Hospital of Sun Yat-sen University Guangzhou 510080, Guangdong Province, China.
Am J Transl Res ; 11(10): 6600-6618, 2019.
Article em En | MEDLINE | ID: mdl-31737211
ABSTRACT
LncRNA is gradually considered as a vital regulator in various physiological and pathological processes. Recently, the role of LINC01234 in several cancers has been reported. However, the function and underlying regulatory mechanism of LINC01234 in multiple myeloma (MM) remain unclear. Our results indicated that LINC01234 was over-expressed in tumor tissues of MM patients, and LINC01234 down-regulation remarkably inhibited cell proliferation, cycle progression and promoted cell apoptosis in MM cells. Mechanistic studies revealed that LINC01234 could sponge miR-124-3p and decreased its expression, thereby up-regulated the protein level of miR-124-3p's targets growth factor receptor-bound protein 2 (GRB2). Additionally, in vivo experiments revealed that LINC01234 shRNA could serve as a tumor suppressor through down-regulating GRB2 in MM. In this study, a novel established regulatory manner of LINC01234/miR-124-3p/GRB2 axis was systematically studied, which may hold promise as a promising target for MM treatment.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Am J Transl Res Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Am J Transl Res Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China