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.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI

祝大家在新的一年里科研腾飞
更新
大幅提高文件上传限制,最高150M (2024-4-1)

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
Hello应助桃井尤川采纳,获得10
5秒前
Young完成签到,获得积分10
10秒前
cyx完成签到,获得积分10
11秒前
思源应助fjiang2003采纳,获得10
11秒前
orixero应助淋湿巴黎采纳,获得10
11秒前
cyx发布了新的文献求助10
14秒前
lu完成签到,获得积分10
16秒前
薄荷味完成签到,获得积分10
17秒前
jimskylxk发布了新的文献求助10
17秒前
18秒前
汉堡包应助坚强莺采纳,获得10
18秒前
无名老大应助fjiang2003采纳,获得30
18秒前
star009完成签到,获得积分10
19秒前
returno_0发布了新的文献求助10
23秒前
希望天下0贩的0应助海蓝采纳,获得10
26秒前
27秒前
星辰大海应助fjiang2003采纳,获得10
27秒前
29秒前
科研通AI2S应助羊沛蓝采纳,获得10
30秒前
淋湿巴黎发布了新的文献求助10
35秒前
35秒前
40秒前
无语完成签到 ,获得积分10
40秒前
lxy完成签到,获得积分10
43秒前
皮皮龙OVO发布了新的文献求助10
44秒前
薄荷味发布了新的文献求助10
48秒前
糟糕的铁锤发布了新的文献求助150
48秒前
Cheng完成签到 ,获得积分10
54秒前
淋湿巴黎完成签到,获得积分10
56秒前
56秒前
iwhsgfes完成签到,获得积分10
57秒前
57秒前
科研通AI2S应助小马哥采纳,获得10
59秒前
星辰大海应助McGrady采纳,获得10
59秒前
胡乱说兔的熊完成签到,获得积分10
1分钟前
尼古拉斯大唯完成签到,获得积分10
1分钟前
1分钟前
ivy发布了新的文献求助10
1分钟前
Nik- KC完成签到 ,获得积分10
1分钟前
1分钟前
高分求助中
Востребованный временем 2500
Production Logging: Theoretical and Interpretive Elements 2000
The Restraining Hand: Captivity for Christ in China 500
The Collected Works of Jeremy Bentham: Rights, Representation, and Reform: Nonsense upon Stilts and Other Writings on the French Revolution 320
Encyclopedia of Mental Health Reference Work 300
脑血管病 300
The Unity of the Common Law 300
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 物理化学 催化作用 细胞生物学 免疫学 冶金
热门帖子
关注 科研通微信公众号,转发送积分 3371928
求助须知:如何正确求助?哪些是违规求助? 2989889
关于积分的说明 8737568
捐赠科研通 2673172
什么是DOI,文献DOI怎么找? 1464391
科研通“疑难数据库(出版商)”最低求助积分说明 677506
邀请新用户注册赠送积分活动 668867