Acidic environment modifies heat- or radiation-induced apoptosis in human maxillary cancer cells

Citation
T. Ohtsubo et al., Acidic environment modifies heat- or radiation-induced apoptosis in human maxillary cancer cells, INT J RAD O, 49(5), 2001, pp. 1391-1398
Citations number
25
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Onconogenesis & Cancer Research
Journal title
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS
ISSN journal
03603016 → ACNP
Volume
49
Issue
5
Year of publication
2001
Pages
1391 - 1398
Database
ISI
SICI code
0360-3016(20010401)49:5<1391:AEMHOR>2.0.ZU;2-V
Abstract
Purpose: The effects of hyperthermia or irradiation on cell killing and ind uction of apoptosis were evaluated using human maxillary carcinoma IMC-3 ce lls and low pH (pH 6.8) adapted cells (IMC-3-pH). Methods and Materials: Cellular heat-sensitivity or radiosensitivity was de termined using the clonogenic assay. Apoptosis was assessed on the basis of a flow cytometric determination of the DNA content, DNA fragmentation, and poly(ADP-ribose)polymerase cleavage. Results: When IMC-3 cells or IMC-3-pH cells were exposed to heat at 44 degr eesC in pH 6.8 medium, an increase in thermosensitivity was observed compar ed with when the IMC-3 cells were exposed to heat at 44 degreesC in pH 7.4 medium. However, the selective reduction in survival was not observed after irradiation. In IMC-3 cells, apoptosis after heating at 44 degreesC for 60 min in pH 7.4 medium occurred earlier than that after 8 Gy irradiation, al though both thermal and irradiated doses decreased the cell count to 10%. T he degree of apoptosis after heating at pK 6.8 in IMC-3 cells or IMC-3 pH c ells was greater than that at pH 7.4 in IMC-3 cells. However, the degree of apoptosis after 8 Gy irradiation at pH 6.8 in IMC-3 cells or IMC-3-pH cell s was smaller than that at pH 7.4 in IMC-3 cells. Conclusion: Hyperthermia treatment is more effective at inducing apoptosis than radiation is in tumors that contain a population of low pH adapted cel ls. (C) 2001 Elsevier Science Inc.