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

AI Article Synopsis

  • Medicinal herbs have historically played a key role in treating various ailments, including cancer, with compounds like guggulsterone (GS) from the Commiphora mukul tree showing promise as an anticancer agent.
  • GS has been studied for its ability to induce cell death in cancer cells by targeting critical survival pathways such as JAK/STAT, NF-kB, and PI3-kinase/AKT, which help regulate cancer cell growth and inflammation.
  • Future research is necessary to establish effective dosages for humans and to create new forms of GS that enhance its therapeutic effects, paving the way for its application in cancer treatment.

Article Abstract

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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Source
http://dx.doi.org/10.1002/cbin.12112DOI Listing

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