熊果酸三萜天然产物对膀胱和卵巢肿瘤细胞系的抗增殖作用

IF 4.2 4区 医学 Q2 CHEMISTRY, MEDICINAL
Lídia Walter de Paula e Silva, Tamires Cunha Almeida, Mariane Ster da Silva Teixeira, Clara Maria Villela Cerrutti, Lívia da Cunha Agostini, Geraldo Celio Brandão, Glenda Nicioli da Silva
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引用次数: 0

摘要

由于膀胱癌和卵巢癌的高发病率、高死亡率以及与早期诊断相关的挑战,它们给卫生保健系统带来了沉重的负担。目前的化疗方案通常涉及药物组合,通常会导致严重的副作用,对患者的依从性和治疗效果产生负面影响。最近,研究探索了使用草药来减轻化疗的不良反应。其中一种草药化合物是熊果酸(UA),一种以抗炎、抗氧化和抗肿瘤特性而闻名的三萜。本研究旨在通过细胞毒性、克隆存活、细胞迁移、形态学变化、细胞凋亡、细胞周期分析、JHDM1D表达和MRC-5细胞的选择性等多种实验,以及计算机评价,评估UA对携带TP53突变的膀胱癌和卵巢癌细胞的影响。该治疗对肿瘤细胞具有选择性,在两种细胞类型中均具有显著的抗增殖作用,导致细胞活力降低,集落形成能力降低,细胞迁移受到抑制,细胞死亡特征的形态学改变,以及JHDM1D的表达增加。总之,UA对不同TP53突变位点的膀胱癌和卵巢癌细胞系显示出抗增殖活性,表明其作为一种有前景的治疗选择的潜力。此外,我们的研究也首次证实了UA在F. formosa物种中的存在。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Antiproliferative Effects of the Triterpene Ursolic Acid Natural Product in Bladder and Ovarian Tumor Cell Lines

Antiproliferative Effects of the Triterpene Ursolic Acid Natural Product in Bladder and Ovarian Tumor Cell Lines

Antiproliferative Effects of the Triterpene Ursolic Acid Natural Product in Bladder and Ovarian Tumor Cell Lines

Bladder and ovarian cancers impose a significant burden on healthcare systems due to their high incidence, mortality rates, and the challenges associated with early diagnosis. Current chemotherapy regimens, which typically involve combinations of drugs, often cause severe side effects that negatively impact patient adherence and treatment efficacy. Recently, studies have explored the use of herbal medicines to mitigate the adverse effects of chemotherapy. One such herbal compound is ursolic acid (UA), a triterpene known for its anti-inflammatory, antioxidant, and antitumor properties. This study aimed to evaluate the effects of UA on bladder and ovarian cancer cells harboring TP53 mutations through various assays, including cytotoxicity, clonogenic survival, cell migration, morphological changes, apoptosis, cell cycle analysis, JHDM1D expression and selectivity using MRC-5 cells, along with in silico evaluation. The treatment demonstrated selectivity for tumoral cells and significant antiproliferative effects in both cell types, leading to decreased cell viability, reduced colony-forming ability, inhibited cell migration, morphological changes characteristic of cell death, and increased expression of JHDM1D. In conclusion, UA exhibited antiproliferative activity against bladder and ovarian cancer cell lines with different TP53 mutation sites, suggesting its potential as a promising therapeutic alternative. Moreover, our study demonstrated for the first time the presence of UA in the species F. formosa.

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来源期刊
CiteScore
6.40
自引率
2.60%
发文量
104
审稿时长
6-12 weeks
期刊介绍: Drug Development Research focuses on research topics related to the discovery and development of new therapeutic entities. The journal publishes original research articles on medicinal chemistry, pharmacology, biotechnology and biopharmaceuticals, toxicology, and drug delivery, formulation, and pharmacokinetics. The journal welcomes manuscripts on new compounds and technologies in all areas focused on human therapeutics, as well as global management, health care policy, and regulatory issues involving the drug discovery and development process. In addition to full-length articles, Drug Development Research publishes Brief Reports on important and timely new research findings, as well as in-depth review articles. The journal also features periodic special thematic issues devoted to specific compound classes, new technologies, and broad aspects of drug discovery and development.
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