Division of Science and Technology, Department of Botany, University of Education, Lahore, Punjab, Pakistan.
Department of Botany, Bacha Khan University, Charsadda, Khyber Pakhtunkhwa, Pakistan.
Cell Biol Int. 2024 Feb;48(2):128-142. doi: 10.1002/cbin.12112. Epub 2023 Dec 26.
Throughout human history, the utilization of medicinal herbs has been recognized as a crucial defense against various ailments, including cancer. Natural products with potential anticancer properties, capable of inducing apoptosis in cancer cells, have garnered substantial attention. One such agent under investigation is guggulsterone (GS), a phytosterol derived from the gum resin of the Commiphora mukul tree. This review aims to provide a comprehensive summary of recent studies elucidating the anticancer molecular mechanisms and molecular targets of GS, guiding future research and potential applications as an adjuvant drug in cancer therapy. Recent in vivo and in vitro studies have explored the biological activities of the active ingredients in Commiphora mukul. Specifically, GS emerges as a potential cancer chemopreventive and therapeutic agent. The investigations delve into the impact of GS on constitutively activated survival pathways, including Janus kinase/signal transducer and activator of transcription (JAK/STAT), nuclear factor-kappa B (NF-kB), and PI3-kinase/AKT signaling pathways. These pathways regulate antiapoptotic and proinflammatory genes, exerting control over growth and inflammatory responses. The findings highlight the potential of GS in disrupting survival pathways crucial for cancer cell viability. The inhibition of JAK/STAT, NF-kB, and PI3-kinase/AKT signaling pathways positions GS as a promising candidate for cancer therapy. The review synthesizes evidence from diverse studies, underscoring the multifaceted biological activities of GS in cancer prevention and treatment. To advance our understanding, future clinical and translational studies are imperative to determine effective doses in humans. Additionally, there is a need for the development of new pharmaceutical forms of GS to optimize therapeutic effects. This comprehensive review provides a foundation for ongoing research, offering insights into the potential of GS as a valuable addition to the armamentarium against cancer.
纵观人类历史,药用植物的利用一直被认为是抵御各种疾病(包括癌症)的重要手段。具有诱导癌细胞凋亡的潜在抗癌特性的天然产物已引起广泛关注。一种正在研究的药物是芝麻素(GS),它是从 Commiphora mukul 树的胶树脂中提取的植物甾醇。本综述旨在全面总结最近阐明 GS 的抗癌分子机制和分子靶点的研究,为未来的研究和作为癌症治疗辅助药物的潜在应用提供指导。最近的体内和体外研究探讨了 Commiphora mukul 中活性成分的生物学活性。具体而言,GS 是一种有潜力的癌症化学预防和治疗药物。研究深入探讨了 GS 对组成性激活的存活途径的影响,包括 Janus 激酶/信号转导和转录激活因子(JAK/STAT)、核因子-κB(NF-κB)和 PI3-激酶/AKT 信号通路。这些途径调节抗凋亡和促炎基因,对生长和炎症反应进行控制。研究结果强调了 GS 在破坏对癌细胞存活至关重要的存活途径方面的潜力。抑制 JAK/STAT、NF-κB 和 PI3-激酶/AKT 信号通路使 GS 成为癌症治疗的有前途的候选药物。该综述综合了来自不同研究的证据,强调了 GS 在癌症预防和治疗中的多方面生物学活性。为了推进我们的理解,未来的临床和转化研究对于确定人类的有效剂量至关重要。此外,需要开发 GS 的新药物形式,以优化治疗效果。本综述为正在进行的研究提供了基础,为 GS 作为对抗癌症的有价值的武器提供了深入的见解。