Combating anoikis resistance: bioactive compounds transforming prostate cancer therapy.

IF 1.8 4区 医学 Q3 ONCOLOGY Anti-Cancer Drugs Pub Date : 2024-09-01 Epub Date: 2024-05-14 DOI:10.1097/CAD.0000000000001616
Shweta Gulia, Prakash Chandra, Asmita Das
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Abstract

The study aims to discuss the challenges associated with treating prostate cancer (PCa), which is known for its complexity and drug resistance. It attempts to find differentially expressed genes (DEGs), such as those linked to anoikis resistance and circulating tumor cells, in PCa samples. This study involves analyzing the functional roles of these DEGs using gene enrichment analysis, and then screening of 102 bioactive compounds to identify a combination that can control the expression of the identified DEGs. In this study, 53 DEGs were identified from PCa samples including anoikis-resistant PCa cells and circulating tumor cells in PCa. Gene enrichment analysis with regards to functional enrichment of DEGs was performed. An inclusive screening process was carried out among 102 bioactive compounds to identify a combination capable of affecting and regulating the expression of selected DEGs. Eventually, gastrodin, nitidine chloride, chenodeoxycholic acid, and bilobalide were selected, as their combination demonstrated ability to modulate expression of 50 out of the 53 genes targeted. The subsequent analysis focused on investigating the biological pathways and processes influenced by this combination. The findings revealed a multifaceted and multidimensional approach to tumor regression. The combination of bioactive compounds exhibited effects on various genes including those related to production of inflammatory cytokines, cell proliferation, autophagy, apoptosis, angiogenesis, and metastasis. The current study has made a valuable contribution to the development of a combination of bioactive natural compounds that can significantly impede the development of treatment resistance in prostate tumor while countering the tumors' evasion of the immune system. The implications of this study are highly significant as it suggests the creation of an enhanced immunotherapeutic, natural therapeutic concoction with combinatorial potential.

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对抗抗药性:生物活性化合物改变前列腺癌疗法。
该研究旨在讨论与治疗前列腺癌(PCa)相关的挑战,众所周知,前列腺癌具有复杂性和耐药性。该研究试图在 PCa 样本中发现差异表达基因(DEG),如与耐药性和循环肿瘤细胞相关的基因。这项研究包括利用基因富集分析法分析这些 DEGs 的功能作用,然后筛选 102 种生物活性化合物,找出能够控制已识别 DEGs 表达的组合。本研究从 PCa 样本中发现了 53 个 DEGs,其中包括耐 anoikis PCa 细胞和 PCa 中的循环肿瘤细胞。对 DEGs 的功能富集进行了基因富集分析。对 102 种生物活性化合物进行了全面筛选,以确定能够影响和调节所选 DEGs 表达的组合。最终,天麻素、氯化亚硝胺、去氧胆酸和比洛巴利肽被选中,因为它们的组合能够调节 53 个目标基因中 50 个基因的表达。随后的分析侧重于研究受这一组合影响的生物途径和过程。研究结果揭示了一种多方面、多维度的肿瘤消退方法。生物活性化合物组合对多种基因产生了影响,包括与炎症细胞因子的产生、细胞增殖、自噬、细胞凋亡、血管生成和转移相关的基因。目前的研究为开发一种生物活性天然化合物组合做出了宝贵的贡献,这种化合物组合能够显著阻碍前列腺肿瘤抗药性的产生,同时对抗肿瘤对免疫系统的逃避。这项研究的意义非常重大,因为它提出了一种具有组合潜力的增强型免疫疗法和天然疗法。
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来源期刊
Anti-Cancer Drugs
Anti-Cancer Drugs 医学-药学
CiteScore
3.80
自引率
0.00%
发文量
244
审稿时长
3 months
期刊介绍: Anti-Cancer Drugs reports both clinical and experimental results related to anti-cancer drugs, and welcomes contributions on anti-cancer drug design, drug delivery, pharmacology, hormonal and biological modalities and chemotherapy evaluation. An internationally refereed journal devoted to the fast publication of innovative investigations on therapeutic agents against cancer, Anti-Cancer Drugs aims to stimulate and report research on both toxic and non-toxic anti-cancer agents. Consequently, the scope on the journal will cover both conventional cytotoxic chemotherapy and hormonal or biological response modalities such as interleukins and immunotherapy. Submitted articles undergo a preliminary review by the editor. Some articles may be returned to authors without further consideration. Those being considered for publication will undergo further assessment and peer-review by the editors and those invited to do so from a reviewer pool.
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