光化性角化病发生的分子机制分析

Yu.V. Tepliuk
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引用次数: 0

摘要

目的探讨光化性角化病(AK)发生的分子机制,并与Bowen病进行比较。材料和方法。文献回顾,分析国家和国际协议诊断AK提出,符合选择标准。我们回顾了2015年以后发表的至少有一项推荐AK诊断方案的作品。系统的文献综述是基于包含某些原癌基因的分子诊断描述的现代研究,以建立最终诊断。还审查了跨学科指南,以进一步探索所有可能的诊断标准。结果和讨论。到目前为止,还没有对AK发育的分子机制进行充分的研究和归纳。在大多数文献中,只有p53蛋白被认为是调控细胞凋亡的主要转录因子。然而,最近的研究证明CD95的影响是充分的,它与p53一样,诱导细胞凋亡,在AK的发生发展中起主导作用。所有的皮肤癌前肿瘤和恶性肿瘤都是由于细胞突变引起的,细胞突变会导致细胞凋亡的破坏,但目前还没有建议和明确的诊断算法,可以快速建立最终诊断并选择这种或另一种治疗方法。结论。AK和Bowen病是同一恶性过程发展的不同阶段,细胞的增殖活性和原癌基因CD95、bcl-2和p16的表达不同,可作为鉴别诊断标志物。由于早期诊断,有可能选择最合适的治疗方案,并考虑到现代协议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of molecular mechanisms of development of actinic keratosis: a review
Objective — to study the molecular mechanisms of the development of actinic keratosis (AK) and compare them with Bowen’s disease. Materials and methods. A literature review, analysis of national and international protocols for the diagnosis of AK are presented, which meet the selection criteria. We reviewed works with at least one recommendation for AK diagnostic scenario published after 2015. The systematic literature review is based on modern studies containing descriptions of molecular diagnostics of certain proto-oncogenes to establish the final diagnosis. Interdisciplinary guidelines were also reviewed to further explore all possible diagnostic criteria. Results and discussion. Until now, the molecular mechanisms of AK development have not been fully studied and grouped into a single review. In most of the sources, only p53 protein was mentioned as the main transcription factor regulating apoptosis. However, recent studies prove a sufficient influence of CD95, which, like p53, induces apoptosis and plays a leading role in the development of AK. All precancerous and malignant neoplasms of the skin arise due to mutations in cells, which cause a violation of apoptosis, but there are still no recommendations and a clear diagnostic algorithm that will allow to quickly establish the final diagnosis and make a choice in favor of this or another method of treatment. Conclusions. AK and Bowen’s disease are different stages in the development of the same malignant process, differing in the proliferative activity of cells and the expression of proto-oncogenes CD95, bcl-2, and p16 which can be used as differential diagnostic markers. Thanks to early diagnosis, it is possible to choose the most suitable treatment option, with consideration for modern protocols.
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