STUDIES ON THE EFFECT OF A NEW RADIOSENSITIZER CM ON THE DNase ACTIVITY OF IRRADIATED HEPATIC TUMOR CELLS
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STUDIES ON THE EFFECT OF A NEW RADIOSENSITIZER CM ON THE DNase ACTIVITY OF IRRADIATED HEPATIC TUMOR CELLS
Journal of Radiation Research and Radiation ProcessingVol. 9, Issue 2, Pages: 65-68(1991)
作者机构:
第二军医大学,上海
作者简介:
基金信息:
DOI:
CLC:
Published:1991-05,
Received:04 October 1989,
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Zhao Fang, Zheng Xiulong. STUDIES ON THE EFFECT OF A NEW RADIOSENSITIZER CM ON THE DNase ACTIVITY OF IRRADIATED HEPATIC TUMOR CELLS. [J]. Journal of Radiation Research and Radiation Processing, 1991,9(2):65-68.
DOI:
Zhao Fang, Zheng Xiulong. STUDIES ON THE EFFECT OF A NEW RADIOSENSITIZER CM ON THE DNase ACTIVITY OF IRRADIATED HEPATIC TUMOR CELLS. [J]. Journal of Radiation Research and Radiation Processing, 1991,9(2):65-68.DOI:
STUDIES ON THE EFFECT OF A NEW RADIOSENSITIZER CM ON THE DNase ACTIVITY OF IRRADIATED HEPATIC TUMOR CELLS
The effects of a new radiosensitizing compound-metronidazolamic acid(CM) and its Ca
+2
chelation compound (CMCa) on the DNase activity of mouse hepatic tumor (H
22
) cells were observed.The effects of CM
CMCa or Ca
+2
at same molarity and their combination with γ-rays irradiation on DNase activity of H
22
cells were also observed respectively. The results showed that CM could activate the DNase activity to be increased as CM concentration increased below 5 mmol/L. The highest DNase activity was activated by CM at 5 mmol/L. The degree of activation between CM and CMCa had no significant differente (p
>
0.05)
whereas free Ca
+2
alone had no effect. The activation of combined CM or CMCa and radiation groups were greater than that of each given indep
endently (Fig. 3)
they possessed a coordinate activation. However free Ca
+2
still could not activate the DNase activity after γ-irradiation. From all the above results
it is suggested that CM or CMCa improved the tumor radiotherapeutic efficiency probable due to its activation the DNase activity of cancer cells which enhanced the DNA damage. It might be one of the radiosensitizing mechanism in tumor radiothorapy.