[Expression of FLI-1 and analysis of prognostic factors in primitive neuroectodermal tumor]

Zhonghua Zhong Liu Za Zhi. 2010 Dec;32(12):917-20.
[Article in Chinese]

Abstract

Objective: To observe the expression of FLI-1 in primitive neuroectodermal tumors (PNET), explore the value of immunohistochemical staining of FLI-1 in combination with other neural markers in diagnosis of PNET, and analyze the prognostic factors in PNET patients.

Methods: 35 cases of PNET, of which 33 cases with complete clinical data, were included in this study. Immmunohistochemistry (The En Vision method) was applied to detect the expression of FLI-1, CD99, Syn, NSE, S-100, NF, Vim in the tumor tissues. The clinicopathological data of 33 cases were analyzed by Cox regression.

Results: The positive expression rate of FLI-1 were 51.4% and that of CD99 was 88.6%. The sensitivity of FLI-1 combined with CD99 was up to 100%. The positive rates of Vim, Syn, NSE, s-100 and NF were 91.4%, 48.6%, 45.7%, 22.9% and 0, respectively. Cox regression analysis showed that the impact of primary location and treatment modality were of statistical significance (P < 0.05), but the age, sex, stage or size of tumors did not (P > 0.05).

Conclusion: Immunohistochemical detection of FLI-1 and neural markers is a preferred method for clinical diagnosis of PNET. The main factors affecting the prognosis are the primary location of PNET and treatment modality.

MeSH terms

  • 12E7 Antigen
  • Adolescent
  • Adult
  • Antigens, CD / metabolism
  • Brain Neoplasms* / metabolism
  • Brain Neoplasms* / pathology
  • Brain Neoplasms* / therapy
  • Cell Adhesion Molecules / metabolism
  • Child
  • Child, Preschool
  • Combined Modality Therapy
  • Female
  • Follow-Up Studies
  • Humans
  • Infant
  • Male
  • Middle Aged
  • Neuroectodermal Tumors, Primitive* / metabolism
  • Neuroectodermal Tumors, Primitive* / pathology
  • Neuroectodermal Tumors, Primitive* / therapy
  • Neuroectodermal Tumors, Primitive, Peripheral* / metabolism
  • Neuroectodermal Tumors, Primitive, Peripheral* / pathology
  • Neuroectodermal Tumors, Primitive, Peripheral* / therapy
  • Pelvic Neoplasms* / metabolism
  • Pelvic Neoplasms* / pathology
  • Pelvic Neoplasms* / therapy
  • Phosphopyruvate Hydratase / metabolism
  • Proportional Hazards Models
  • Proto-Oncogene Protein c-fli-1 / metabolism*
  • S100 Proteins / metabolism
  • Survival Rate
  • Synaptophysin / metabolism
  • Vimentin / metabolism
  • Young Adult

Substances

  • 12E7 Antigen
  • Antigens, CD
  • CD99 protein, human
  • Cell Adhesion Molecules
  • FLI1 protein, human
  • Proto-Oncogene Protein c-fli-1
  • S100 Proteins
  • Synaptophysin
  • Vimentin
  • Phosphopyruvate Hydratase