[The expression of CXCR4 on acute leukemia cells and its implication for extramedullary infiltration]

Zhonghua Xue Ye Xue Za Zhi. 2004 Jul;25(7):405-8.
[Article in Chinese]

Abstract

Objective: To study the expression of CXCR4 in acute leukemic cells and its clinical significance.

Method: Bone marrow samples from 73 acute leukemia patients and leukemic cell lines were investigated by flow cytometry (FCM), the expression of SDF-1 in human marrow stromal cells and meninges were studied by using reverse transcription polymerase chain reaction (RT-PCR). Adhesion, migration and invasion of U937, NB4 and K562 cells were studied in vitro.

Results: The expression rates of CXCR4 in ALL and AML patients was 65.6% and 17.1%, respectively. And it was 0.2%, 41.0% and 52.0% in K562, U937 and NB4 cells, respectively. The extramedullary infiltration rates were 61.9% and 18.2% for CXCR4 positive and negative groups of ALL, respectively (P < 0.05); while in AML, the number of peripheral white blood cells in CXCR4 positive group was lower than that in CXCR4 negative group (P < 0.05). SDF-1alpha could enhance the adhesion, migration and invasion capacity of leukemic cells in vitro.

Conclusion: Overexpression of CXCR4 in AL cells might be the molecular mechanism of extramedullary infiltration in leukemia.

Publication types

  • English Abstract

MeSH terms

  • Acute Disease
  • Adolescent
  • Adult
  • Aged
  • Bone Marrow Cells / metabolism
  • Bone Marrow Cells / pathology
  • Cell Adhesion
  • Cell Line, Tumor
  • Cell Movement
  • Chemokine CXCL12 / genetics
  • Female
  • Fibroblasts / metabolism
  • Fibroblasts / pathology
  • Flow Cytometry
  • Gene Expression Regulation, Neoplastic
  • Humans
  • K562 Cells
  • Leukemia / genetics
  • Leukemia / metabolism
  • Leukemia / pathology*
  • Leukemic Infiltration / metabolism
  • Leukemic Infiltration / pathology*
  • Male
  • Meninges / metabolism
  • Meninges / pathology
  • Middle Aged
  • Receptors, CXCR4 / biosynthesis*
  • Reverse Transcriptase Polymerase Chain Reaction
  • U937 Cells

Substances

  • Chemokine CXCL12
  • Receptors, CXCR4