Current stage of preclinical and clinical development of guggulsterone in cancers: Challenges and promises

蛋白激酶B 癌症 贾纳斯激酶 癌症研究 STAT蛋白 癌细胞 斯达 癌变 信号转导 生物 PI3K/AKT/mTOR通路 车站3 药理学 医学 内科学 细胞生物学
作者
Shumaila Ijaz,Javed Iqbal,Bilal Haider Abbasi,Aasma Tufail,Tabassum Yaseen,Siraj Uddin,Kiran Usman,Rafi Ullah,Hafsa Bibi,Palwasha Inam,Elvira Sagindykova,Eda Sönmez Gürer,Solomon Habtemariam,Daniela Călina,Javad Sharifi‐Rad
出处
期刊:Cell Biology International [Wiley]
标识
DOI:10.1002/cbin.12112
摘要

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.
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