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Retraction of: A005, a novel inhibitor of phosphatidylinositol 3-kinase/mammalian target of rapamycin, prevents osteosarcoma-induced osteolysis.
Lian, Zhen; Han, Jinsong; Huang, Lin; Wei, Chengming; Fan, Yongyong; Xu, Jiake; Zhou, Mengyu; Feng, Haotian; Liu, Qian; Chen, Lingzi; Li, Zhaoning; Cheng, Haichun; Yuan, Guixin; Lin, Xixi; Song, Fangming; Su, Yiji; Wang, Chao; Huang, Guopeng; Qin, An; Song, Yunlong; Yao, Guanfeng.
Afiliação
  • Lian Z; Department of Orthopedics, The Second Affiliated Hospital, Shantou University Medical College, Shantou, Guangdong, China.
  • Han J; Department of Medicinal Chemistry, School of Pharmacy, Second Military Medical University, Shanghai, China.
  • Huang L; Department of Medicinal Chemistry, Organisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld, Heidelberg, Germany.
  • Wei C; Department of Spine Surgery, Department of Orthopedics, Research Center of Spinal and Pelvic Tumor, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou City, Guangdong Province, China.
  • Fan Y; Department of Orthopedics, Collaborative Innovation Center of Guangxi Biological Medicine, Guangxi Medical University, Guangxi, China.
  • Xu J; Orthopedic Department, Taizhou Hospital, Wenzhou Medical University, Linhai, China.
  • Zhou M; Department of Orthopedics, School of Pathology and Laboratory Medicine, The University of Western Australia, Perth, Western Australia, Australia.
  • Feng H; Department of Stomatology, Haicheng Central Hospital, Liaoning, China.
  • Liu Q; Department of Orthopedics, Research Centre for Regenerative Medicine, Guangxi Medical University, Guangxi, China.
  • Chen L; Department of Orthopedics, Research Centre for Regenerative Medicine, Guangxi Medical University, Guangxi, China.
  • Li Z; Department of Orthopedics, The Second Affiliated Hospital, Shantou University Medical College, Shantou, Guangdong, China.
  • Cheng H; Department of Orthopedics, The Second Affiliated Hospital, Shantou University Medical College, Shantou, Guangdong, China.
  • Yuan G; Department of General Surgery, The Shenzhen Shajing Affiliated Hospital of Guangzhou Medical University, Shenzhen, Guangdong, China.
  • Lin X; Department of Orthopedics, The Second Affiliated Hospital, Shantou University Medical College, Shantou, Guangdong, China.
  • Song F; Department of Orthopedics, Research Centre for Regenerative Medicine, Guangxi Medical University, Guangxi, China.
  • Su Y; Department of Orthopedics, Research Centre for Regenerative Medicine, Guangxi Medical University, Guangxi, China.
  • Wang C; Department of Rehabilitation, The First Affiliated Hospital, Guangxi Medical University, Guangxi, China.
  • Huang G; Department of Orthopedics, School of Pathology and Laboratory Medicine, The University of Western Australia, Perth, Western Australia, Australia.
  • Qin A; Department of Orthopedics, The Second Affiliated Hospital, Shantou University Medical College, Shantou, Guangdong, China.
  • Song Y; Shanghai Key Laboratory of Orthopedic Implants, Department of Orthopedics, Shanghai Ninth People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
  • Yao G; Department of Medicinal Chemistry, School of Pharmacy, Second Military Medical University, Shanghai, China.
Carcinogenesis ; 40(2): e1-e13, 2019 04 29.
Article em En | MEDLINE | ID: mdl-29635391
ABSTRACT
Osteosarcoma is the most frequent primary bone tumor in children and adolescents. The phosphatidylinositol 3-kinase (PI3K)/mammalian target of rapamycin (mTOR) signaling pathway is an attractive anticancer target because it plays key roles in the regulation of cell growth, division and differentiation. In this study, we demonstrated high expression of PI3K/mTOR signaling pathway-related genes in patients with osteosarcoma. We thus investigated the effects of A005, a newly synthesized dual PI3K/mTOR inhibitor, on osteosarcoma cells and in a mouse xenograft tumor model. The results confirmed that A005 inhibited the proliferation, migration and invasion of human osteosarcoma cells. In addition, A005 also inhibited receptor activator of nuclear factor kappa-B ligand (RANKL)-induced osteoclast differentiation and bone resorption in vitro. Therefore, A005 was further applied to a SaOS-2 osteosarcoma-induced mouse osteolysis model. A005 inhibited tumor growth and prevented osteosarcoma-associated osteolysis via modulation of the PI3K/AKT/mTOR pathway. Overall, our results showed that A005 inhibited osteoclastogenesis and prevented osteosarcoma-induced bone osteolysis by suppressing PI3K/AKT/mTOR signaling. These findings indicated that A005 may be a promising candidate drug for the treatment of human osteosarcoma.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Carcinogenesis Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Carcinogenesis Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China