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外阴癌光动力疗法(PDT)耐药机制。

Mechanisms of Resistance to Photodynamic Therapy (PDT) in Vulvar Cancer.

机构信息

Department of Molecular and Translational Oncology, Maria Skłodowska-Curie National Research Institute of Oncology, Roentgena 5, 02-781 Warsaw, Poland.

Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Pawińskiego 5a, 02-106 Warsaw, Poland.

出版信息

Int J Mol Sci. 2022 Apr 8;23(8):4117. doi: 10.3390/ijms23084117.

Abstract

Photodynamic therapy (PDT) is a valuable treatment method for vulvar intraepithelial neoplasia (VIN). It allows for the treatment of a multifocal disease with minimal tissue destruction. 5-Aminolevulinic acid (5-ALA) is the most commonly used prodrug, which is converted in the heme pathway to protoporphyrin IX (PpIX), an actual photosensitizer (PS). Unfortunately, not all patients treated with PDT undergo complete remission. The main cause of their failure is resistance to anticancer therapy. In many cancers, resistance to various anticancer treatments is correlated with increased activity of the DNA repair protein apurinic/apyrimidinic endonuclease 1 (APE1). Enhanced activity of drug pumps may also affect the effectiveness of therapy. To investigate whether multidrug resistance mechanisms underlie PDT resistance in VIN, porphyrins were isolated from sensitive and resistant vulvar cancer cells and their culture media. APE1 activity was measured, and survival assay after PDT combined with APE1 inhibitor was performed. Our results revealed that resistant cells accumulated and effluxed less porphyrins than sensitive cells, and in response to PDT, resistant cells increased APE1 activity. Moreover, PDT combined with inhibition of APE1 significantly decreased the survival of PDT-resistant cells. This means that resistance to PDT in vulvar cancer may be the result of alterations in the heme synthesis pathway. Moreover, increased APE1 activity may be essential for the repair of PDT-mediated DNA damage, and inhibition of APE1 activity may increase the efficacy of PDT.

摘要

光动力疗法(PDT)是治疗外阴上皮内瘤变(VIN)的一种有价值的治疗方法。它可以在最小组织损伤的情况下治疗多灶性疾病。5-氨基酮戊酸(5-ALA)是最常用的前体药物,它在血红素途径中转化为原卟啉 IX(PpIX),这是一种实际的光敏剂(PS)。不幸的是,并非所有接受 PDT 治疗的患者都能完全缓解。他们失败的主要原因是对抗癌治疗的耐药性。在许多癌症中,对各种抗癌治疗的耐药性与 DNA 修复蛋白脱嘌呤/脱嘧啶内切酶 1(APE1)的活性增加有关。药物泵的增强活性也可能影响治疗的有效性。为了研究多药耐药机制是否是 VIN 中 PDT 耐药的基础,从敏感和耐药外阴癌细胞及其培养基中分离出卟啉。测量了 APE1 的活性,并进行了 PDT 联合 APE1 抑制剂后生存测定。我们的结果表明,耐药细胞比敏感细胞积累和外排的卟啉更少,并且对 PDT 有反应时,耐药细胞增加了 APE1 的活性。此外,PDT 联合 APE1 抑制显著降低了 PDT 耐药细胞的存活率。这意味着外阴癌中对 PDT 的耐药性可能是血红素合成途径改变的结果。此外,APE1 活性的增加可能是修复 PDT 介导的 DNA 损伤所必需的,抑制 APE1 活性可能会提高 PDT 的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1fd/9028356/65664adcce71/ijms-23-04117-g001.jpg

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