The recent studies about the interaction of phthalocyanine with DNA

E. Bağda, Efkan Bağda
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引用次数: 1

Abstract

Cancer is one of the major diseases affecting all humanity with high mortality rates worldwide. Its treatment is difficult, long-term and expensive. Due to its side effects, it is troublesome for both the patient and their attendants. Cancer treatment is basically divided into three: surgery, chemotherapy and radiotherapy. Photodynamic therapy offers one of the most important and promising treatment methods, especially in recent years. Photodynamic therapy takes the steps of administering the photo-sensitizing compound to the body and stimulating it with a light of appropriate wavelength after its accumulation in the target tissue. With the formation of complex processes that take place in the target area with the reactive oxygen species formed by the stimulated compounds, death or the inhibition of the proliferation of the cells causes situations such as the destruction of the target tissue. Phthalocyanines constitute an important group of photo-sensitizers used in photodynamic therapy. Stability of these compounds and their strong absorption close to therapeutic window make these compounds important. With large Π systems, they can bind with many biological macromolecules, including DNA, with high affinity by many mechanisms, including the Π - Π stacking. This review article describes the last three years of studies in the WOS database about the interactions of phthalocyanines with DNA. The interactions of phthalocyanines with DNA are important as they can make a difference in the proliferation of tumor cells. On the other hand, DNA replication and transcription has increased due to the increasing metabolic rate of these cells. The DNA double strand opened during replication, and gene expression allows the formation of different secondary structures such as hairpin, triple, junctions, and G-quadruplex. The interaction of G-quadruplex DNA structures with these compounds, which can be formed in the guanine-rich regions of the DNA sequences opened in these processes, has been described in studies.
酞菁与DNA相互作用的研究进展
癌症是影响全人类的主要疾病之一,在世界范围内死亡率很高。它的治疗是困难的,长期的和昂贵的。由于它的副作用,对病人和他们的护理人员都很麻烦。癌症治疗基本上分为三种:手术、化疗和放疗。光动力疗法是近年来最重要和最有前途的治疗方法之一。光动力疗法采取的步骤是将光敏化合物施用于身体,并在其在目标组织中积累后用适当波长的光刺激它。随着在靶区与受刺激化合物形成的活性氧形成的复杂过程的形成,细胞的死亡或增殖的抑制导致靶组织的破坏等情况。酞菁是光动力治疗中重要的光敏剂。这些化合物的稳定性和它们在治疗窗口附近的强吸收使这些化合物变得重要。在大型Π系统中,它们可以通过许多机制与包括DNA在内的许多生物大分子结合,具有高亲和力,包括Π - Π堆叠。本文综述了WOS数据库近三年来关于酞菁与DNA相互作用的研究进展。酞菁与DNA的相互作用很重要,因为它们可以对肿瘤细胞的增殖产生影响。另一方面,由于这些细胞代谢率的增加,DNA的复制和转录也增加了。DNA双链在复制过程中打开,基因表达允许形成不同的二级结构,如发夹结构、三重结构、连接结构和g -四重结构。g -四重体DNA结构与这些化合物的相互作用,可以在这些过程中打开的DNA序列的富鸟嘌呤区域形成,已经在研究中描述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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