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,Adnan Tufail,Tabassum Yaseen,Siraj Uddin,Kiran Usman,Rafi Ullah,H. Bibi,Palwasha Inam,Elvira Sagindykova,Eda Sönmez Gürer,Solomon Habtemariam,Daniela Călina,Javad Sharifi‐Rad
出处
期刊:Cell Biology International [Wiley]
卷期号:48 (2): 128-142 被引量:2
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.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
廖婕发布了新的文献求助30
刚刚
dl发布了新的文献求助10
1秒前
stiger应助mmyhn采纳,获得10
5秒前
totojian关注了科研通微信公众号
5秒前
签儿儿儿发布了新的文献求助10
6秒前
无花果应助shsheng采纳,获得10
7秒前
笨笨友安发布了新的文献求助10
8秒前
Amai完成签到,获得积分10
13秒前
小二郎应助科研通管家采纳,获得10
13秒前
小二郎应助科研通管家采纳,获得10
13秒前
桐桐应助科研通管家采纳,获得10
13秒前
桐桐应助科研通管家采纳,获得10
13秒前
CJoanne应助科研通管家采纳,获得10
13秒前
CJoanne应助科研通管家采纳,获得10
13秒前
共享精神应助科研通管家采纳,获得30
13秒前
共享精神应助科研通管家采纳,获得30
14秒前
传奇3应助科研通管家采纳,获得10
14秒前
14秒前
传奇3应助科研通管家采纳,获得10
14秒前
我是老大应助科研通管家采纳,获得10
14秒前
我是老大应助科研通管家采纳,获得10
14秒前
Owen应助科研通管家采纳,获得10
14秒前
Owen应助科研通管家采纳,获得10
14秒前
李健应助科研通管家采纳,获得10
14秒前
dgq_81完成签到,获得积分10
14秒前
李健应助科研通管家采纳,获得10
14秒前
酷波er应助科研通管家采纳,获得10
14秒前
酷波er应助科研通管家采纳,获得10
14秒前
超帅寻双应助科研通管家采纳,获得10
14秒前
小二郎应助科研通管家采纳,获得10
15秒前
15秒前
15秒前
16秒前
今后应助dx采纳,获得10
16秒前
Coisini完成签到,获得积分20
16秒前
科科完成签到,获得积分10
17秒前
三水学姐完成签到,获得积分10
17秒前
18秒前
ding应助花花金兔采纳,获得10
18秒前
zpl完成签到 ,获得积分10
18秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Kinesiophobia : a new view of chronic pain behavior 2000
Research for Social Workers 1000
Mastering New Drug Applications: A Step-by-Step Guide (Mastering the FDA Approval Process Book 1) 800
The Social Psychology of Citizenship 600
Signals, Systems, and Signal Processing 510
Discrete-Time Signals and Systems 510
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5912136
求助须知:如何正确求助?哪些是违规求助? 6831031
关于积分的说明 15784944
捐赠科研通 5037126
什么是DOI,文献DOI怎么找? 2711580
邀请新用户注册赠送积分活动 1661930
关于科研通互助平台的介绍 1603895