Alkaloid-based modulators of the PI3K/Akt/mTOR pathway for cancer therapy: Understandings from pharmacological point of view

IF 4.7 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Chemico-Biological Interactions Pub Date : 2024-08-28 DOI:10.1016/j.cbi.2024.111218
Fatima Zohra Mokhfi , Md Al Amin , Mehrukh Zehravi , Sherouk Hussein Sweilam , Uppuluri Varuna Naga Venkata Arjun , Jeetendra Kumar Gupta , Bhaskar Vallamkonda , Anitha Balakrishnan , Manjula Challa , Jyoti Singh , P. Dharani Prasad , Syed Salman Ali , Irfan Ahmad , Koula Doukani , Talha Bin Emran
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Abstract

This review aims to summarize the role of alkaloids as potential modulators of the PI3K/Akt/mTOR (PAMT) pathway in cancer therapy. The PAMT pathway plays a critical role in cell growth, survival, and metabolism, and its dysregulation contributes to cancer hallmarks. In healthy cells, this pathway is tightly controlled. However, this pathway is frequently dysregulated in cancers and becomes abnormally active. This can happen due to mutations in genes within the pathway itself or due to other factors. This chronic overactivity promotes cancer hallmarks such as uncontrolled cell division, resistance to cell death, and increased blood vessel formation to nourish the tumor. As a result, the PAMT pathway is a crucial therapeutic target for cancer. Researchers are developing drugs that specifically target different components of this pathway, aiming to turn it off and slow cancer progression. Alkaloids, a class of naturally occurring nitrogen-containing molecules found in plants, have emerged as potential therapeutic agents. These alkaloids can target different points within the PAMT pathway, inhibiting its activity and potentially resulting in cancer cell death or suppression of tumor growth. Research is ongoing to explore the role of various alkaloids in cancer treatment. Berberine reduces mTOR activity and increases apoptosis by targeting the PAMT pathway, inhibiting cancer cell proliferation. Lycorine inhibits Akt phosphorylation and mTOR activation, increasing pro-apoptotic protein production and decreasing cell viability. In glioblastoma models, harmine suppresses mTORC1. This review focuses on alkaloids such as evodiamine, hirsuteine, chaetocochin J, indole-3-carbinol, noscapine, berberine, piperlongumine, and so on, which have shown promise in targeting the PAMT pathway. Clinical studies evaluating alkaloids as part of cancer treatment are underway, and their potential impact on patient outcomes is being investigated. In summary, alkaloids represent a promising avenue for targeting the dysregulated PAMT pathway in cancer, and further research is warranted.

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基于生物碱的癌症治疗 PI3K/Akt/mTOR 通路调节剂:从药理学角度理解
本综述旨在总结生物碱作为PI3K/Akt/mTOR(PAMT)通路的潜在调节剂在癌症治疗中的作用。PAMT 通路在细胞生长、存活和新陈代谢中发挥着关键作用,其失调是导致癌症的标志性因素。在健康细胞中,该通路受到严格控制。然而,在癌症中,这条通路经常失调,变得异常活跃。发生这种情况的原因可能是通路本身的基因突变,也可能是其他因素。这种长期的过度活跃促进了癌症的特征,如不受控制的细胞分裂、抵抗细胞死亡和增加血管形成以滋养肿瘤。因此,PAMT 通路是癌症的一个重要治疗靶点。研究人员正在开发专门针对该通路不同成分的药物,旨在关闭该通路并减缓癌症进展。生物碱是一类存在于植物中的天然含氮分子,已成为潜在的治疗药物。这些生物碱可针对 PAMT 通路中的不同点,抑制其活性,并可能导致癌细胞死亡或抑制肿瘤生长。探索各种生物碱在癌症治疗中的作用的研究正在进行中。小檗碱通过靶向 PAMT 通路降低 mTOR 活性,增加细胞凋亡,从而抑制癌细胞增殖。番荔枝碱可抑制 Akt 磷酸化和 mTOR 激活,增加促凋亡蛋白的产生,降低细胞活力。在胶质母细胞瘤模型中,harmine 可抑制 mTORC1。本综述将重点介绍有望靶向 PAMT 通路的生物碱,如 evodiamine、hirsuteine、chaetocochin J、indole-3-carbinol、noscapine、berberine、piperlongumine 等。将生物碱作为癌症治疗的一部分进行评估的临床研究正在进行中,其对患者预后的潜在影响也在调查之中。总之,生物碱是针对癌症中调控失调的 PAMT 通路的一种很有前景的方法,值得进一步研究。
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来源期刊
CiteScore
7.70
自引率
3.90%
发文量
410
审稿时长
36 days
期刊介绍: Chemico-Biological Interactions publishes research reports and review articles that examine the molecular, cellular, and/or biochemical basis of toxicologically relevant outcomes. Special emphasis is placed on toxicological mechanisms associated with interactions between chemicals and biological systems. Outcomes may include all traditional endpoints caused by synthetic or naturally occurring chemicals, both in vivo and in vitro. Endpoints of interest include, but are not limited to carcinogenesis, mutagenesis, respiratory toxicology, neurotoxicology, reproductive and developmental toxicology, and immunotoxicology.
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