Correlation Engine 2.0
Clear Search sequence regions

  • adult (1)
  • bone neoplasms (1)
  • cell (6)
  • cell growth (1)
  • cell movement (1)
  • female (1)
  • gene (2)
  • human (3)
  • leukemia (1)
  • male (1)
  • oncoproteins (1)
  • osteosarcoma (14)
  • patients (3)
  • pim (12)
  • PIM1 (3)
  • PIM2 (1)
  • PIM3 (1)
  • prognosis (3)
  • provirus (1)
  • signal (1)
  • virus (1)
  • Sizes of these terms reflect their relevance to your search.

    The provirus integrating site Moloney murine leukemia virus (PIM) family of serine/threonine protein kinases is composed of three members, PIM1, PIM2 and PIM3, which have been identified as oncoproteins in various malignancies. However, their role in osteosarcoma (OS) remains largely unknown. This study aimed to examine the expression patterns and the clinical significance of PIM kinases in human OS and their biological effects in human OS cell lines. Immunohistochemical staining was used to detect PIM kinases in archived pathologic material from 43 patients with primary OS; in addition, the effects of PIM knockdown and overexpression on the proliferation, migration and invasion of OS cell lines were determined. We observed that all three PIM kinases were frequently expressed in OS, but only PIM1 positive expression was associated with poorer prognosis regarding overall survival of OS patients. In addition, knockdown of PIM kinases notably inhibited OS cell proliferation, migration and invasiveness, whereas overexpression of PIM kinases resulted in increased OS cell growth and motility. This study suggests that PIM1 could be a valuable prognostic marker in patients with OS, and the biological functions of PIM kinase family in the osteosarcoma cell lines indicate that they could serve as potential therapeutic targets for OS.


    Shuai Mou, Guangbin Wang, Ding Ding, Dongdong Yu, Yi Pei, Songling Teng, Qin Fu. Expression and function of PIM kinases in osteosarcoma. International journal of oncology. 2016 Nov;49(5):2116-2126

    Expand section icon Mesh Tags

    Expand section icon Substances

    PMID: 27826617

    View Full Text