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[实验性脑肿瘤的光辐射疗法]

[Photoradiation therapy of experimental brain tumor].

作者信息

Sekimoto T, Hirakawa K, Ueda S, Nakagawa Y, Ibayashi N, Nakamura K

出版信息

No Shinkei Geka. 1985 Sep;13(9):991-6.

PMID:4069317
Abstract

Malignant tumors retain hematoporphyrin to a much greater extent than do normal tissues and can be destroyed by exposure to light. To utilize this mechanism in the treatment of malignant brain tumor, we investigated the antitumor effect of photoradiation on rat and mouse glioma, utilizing hematoporphyrin administration and cold light irradiation. In vitro study of rat glioma (EA285), the tumor cells which were exposed to hematoporphyrin and light irradiation showed marked degeneration in a short time, though no change was found in the control groups of hematoporphyrin administration alone and of light irradiation alone. The subcutaneously transplanted gliomas of rat and mouse also showed the growth inhibition after treatment of hematoporphyrin and light irradiation, though they grew up again. Histological degeneration by this treatment reached about 7 mm depth in the tumor. It was made clear that the effect on gliomas was induced by photosensitization and not by heat. From these results it is concluded that photoradiation therapy would be a great means for adjuvant therapy for malignant brain tumor.

摘要

恶性肿瘤比正常组织能更大程度地保留血卟啉,并且可通过光照被破坏。为了在恶性脑肿瘤治疗中利用这一机制,我们利用血卟啉给药和冷光照射,研究了光辐射对大鼠和小鼠胶质瘤的抗肿瘤作用。在大鼠胶质瘤(EA285)的体外研究中,暴露于血卟啉和光辐射的肿瘤细胞在短时间内显示出明显的退化,而单独给予血卟啉的对照组和单独进行光辐射的对照组均未发现变化。大鼠和小鼠皮下移植的胶质瘤在接受血卟啉和光辐射治疗后也显示出生长抑制,尽管它们后来又重新生长。这种治疗引起的组织学退化在肿瘤中达到约7毫米深度。明确了对胶质瘤的作用是由光致敏而非热诱导的。从这些结果可以得出结论,光辐射疗法将是恶性脑肿瘤辅助治疗的一种重要手段。

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