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内源性原卟啉IX,一种临床上用于光动力疗法的有用光敏剂。

Endogenous protoporphyrin IX, a clinically useful photosensitizer for photodynamic therapy.

作者信息

Kennedy J C, Pottier R H

机构信息

Department of Oncology, Queen's University, Kingston Ont, Canada.

出版信息

J Photochem Photobiol B. 1992 Jul 30;14(4):275-92. doi: 10.1016/1011-1344(92)85108-7.

Abstract

The tissue photosensitizer protoporphyrin IX (PpIX) is an immediate precursor of heme in the biosynthetic pathway for heme. In certain types of cells and tissues, the rate of synthesis of PpIX is determined by the rate of synthesis of 5-aminolevulinic acid (ALA), which in turn is regulated via a feedback control mechanism governed by the concentration of free heme. The presence of exogenous ALA bypasses the feedback control, and thus may induce the intracellular accumulation of photosensitizing concentrations of PpIX. However, this occurs only in certain types of cells and tissues. The resulting tissue-specific photosensitization provides a basis for using ALA-induced PpIX for photodynamic therapy. The topical application of ALA to certain malignant and non-malignant lesions of the skin can induce a clinically useful degree of lesion-specific photosensitization. Superficial basal cell carcinomas showed a complete response rate of approximately 79% following a single exposure to light. Recent preclinical studies in experimental animals and human volunteers indicate that ALA can induce a localized tissue-specific photosensitization if administered by intradermal injection. A generalized but still quite tissue-specific photosensitization may be induced if ALA is administered by either subcutaneous or intraperitoneal injection or by mouth. This opens the possibility of using ALA-induced PpIX to treat tumors that are too thick or that lie too deep to be accessible to either topical or locally injected ALA.

摘要

组织光敏剂原卟啉IX(PpIX)是血红素生物合成途径中血红素的直接前体。在某些类型的细胞和组织中,PpIX的合成速率由5-氨基乙酰丙酸(ALA)的合成速率决定,而ALA的合成速率又通过由游离血红素浓度控制的反馈调节机制来调控。外源性ALA的存在绕过了反馈调节,因此可能会诱导细胞内光敏浓度的PpIX积累。然而,这仅发生在某些类型的细胞和组织中。由此产生的组织特异性光敏化作用为利用ALA诱导的PpIX进行光动力治疗提供了基础。将ALA局部应用于皮肤的某些恶性和非恶性病变可诱导临床上有用的病变特异性光敏化程度。单次光照后,浅表基底细胞癌的完全缓解率约为79%。最近在实验动物和人类志愿者身上进行的临床前研究表明,如果通过皮内注射给予ALA,它可以诱导局部组织特异性光敏化。如果通过皮下或腹腔注射或口服给予ALA,则可能会诱导全身性但仍具有相当组织特异性的光敏化。这为利用ALA诱导的PpIX治疗太厚或太深以至于无法通过局部或局部注射ALA到达的肿瘤开辟了可能性。

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