[Flow cytometry for testing chemosensitivity of malignant bone tumors]

Zhonghua Wai Ke Za Zhi. 1999 Dec;37(12):737-9.
[Article in Chinese]

Abstract

Objective: To study chemosensitivity and multidrug resistance of malignant bone tumors and to make an individual protocol of chemotherapy with sensitive antitumor agents.

Methods: Apoptosis induced by MTX, ADM, MMC, VP-16, VCR and CTX, and chemosensitivity in 32 fresh specimens of malignant bone tumors were analyzed by flow cytometry (FCM) and quantitative immunofluorescence. The expression of P-glycoprotein (P170) in the specimen and the relation between P170, multidrug resistance, and chemosensitivity were detected.

Results: The rate of apoptosis was significantly different in malignant bone tumor cells treated with different drugs: MTX (30.50 +/- 10.22)%, ADM (26.28 +/- 9.35)%, MMC (23.11 +/- 7.38)%, VP-16 (18.17 +/- 6.14)%, VCR (4.44 +/- 2.55)%, and CTX (1.22 +/- 0.59)%. The individual variation of cell apoptosis was prominent in the specimens of same pathological type treated with same agent. There was lower chemosensitivity in the malignant bone tumors with a high expression of P170.

Conclusions: Chemosensitivity testing by flow cytometry is a simple, quick and sensitive assay. Quantitative analysis of expression of P170 could be used to predict multidrug resistance and its chemosensitivity of malignant bone tumors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / biosynthesis*
  • Antineoplastic Agents / pharmacology*
  • Apoptosis / drug effects*
  • Bone Neoplasms / metabolism
  • Bone Neoplasms / pathology*
  • Doxorubicin / pharmacology
  • Drug Resistance, Multiple*
  • Drug Resistance, Neoplasm*
  • Flow Cytometry
  • Fluorouracil / pharmacology
  • Humans
  • Methotrexate / pharmacology
  • Mitomycin / pharmacology
  • Osteosarcoma / metabolism
  • Osteosarcoma / pathology

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Antineoplastic Agents
  • Mitomycin
  • Doxorubicin
  • Fluorouracil
  • Methotrexate