Natural Products Research Laboratory, Department of Pharmaceutical Sciences, School of Applied Sciences & Technology, University of Kashmir, Hazratbal Srinagar, J&K, India.
Centre for Translational and Clinical Research, School of Chemical & Life Sciences, Jamia Hamdard, New Delhi 110062, India.
Curr Med Chem. 2024;31(21):3093-3117. doi: 10.2174/0929867331666230809100335.
Despite substantial advancements in curative modern medicine in the last few decades, cancer risk and casualty rates have continued to mount globally. The exact reason for cancer's onset and progression is still unknown. However, skeletal and functional abnormalities in the genetic code are assumed to be the primary cause of cancer. Many lines of evidence reported that some medicinal plants can be utilized to curb cancer cell proliferation with a safe, fruitful, and cost-efficient perspective. Curcuminoid, isolated from , have gotten a lot of focus due to their anticancer potential as they reduce tumor progression, invasion, and dissemination. Further, they modulated signal transduction routes like MAPK, PI3K/Akt/mTOR, JAK/STAT, and Wnt/β-catenin, etc., and triggered apoptosis as well as actuated autophagy in malignant cells without altering the normal cells, thus preventing cancer progression. Besides, Curcuminoid also regulate the function and expression of anti-tumor and carcinogenic miRNAs. Clinical studies also reported the therapeutic effect of Curcuminoid against various cancer through decreasing specific biomarkers like TNF-α, Bcl-2, COX-2, PGE2, VEGF, IκKβ, and various cytokines like IL-12p70, IL-10, IL-2, IFN-γ levels and increasing in p53 and Bax levels. Thus, in the present review, we abridged the modulation of several signal transduction routes by Curcuminoids in various malignancies, and its modulatory role in the initiation of tumor-suppressive miRNAs and suppression of the oncogenic miRNAs are explored. Additionally, various pharmacokinetic approaches have been projected to address the Curcuminoids bioavailability like the use of piperine as an adjuvant; nanotechnology- based Curcuminoids preparations utilizing Curcuminoids analogues are also discussed.
尽管在过去几十年中,治愈性现代医学取得了重大进展,但癌症的风险和死亡率仍在全球范围内持续上升。癌症发病和进展的确切原因尚不清楚。然而,人们认为遗传密码中的骨骼和功能异常是癌症的主要原因。有许多证据表明,一些药用植物可以用于抑制癌细胞增殖,具有安全、富有成效和具有成本效益的观点。姜黄素,从姜黄中分离出来的,由于其抗癌潜力而受到了很多关注,因为它们可以降低肿瘤的进展、侵袭和扩散。此外,它们还调节了 MAPK、PI3K/Akt/mTOR、JAK/STAT 和 Wnt/β-catenin 等信号转导途径,并在不改变正常细胞的情况下触发恶性细胞的细胞凋亡和自噬,从而阻止癌症的进展。此外,姜黄素还调节抗肿瘤和致癌 miRNA 的功能和表达。临床研究还报告了姜黄素通过降低 TNF-α、Bcl-2、COX-2、PGE2、VEGF、IκKβ 和各种细胞因子如 IL-12p70、IL-10、IL-2、IFN-γ 等特定生物标志物对各种癌症的治疗效果,并增加 p53 和 Bax 水平。因此,在本综述中,我们总结了姜黄素在各种恶性肿瘤中对几种信号转导途径的调节作用,以及其在启动肿瘤抑制 miRNA 和抑制致癌 miRNA 方面的调节作用。此外,还提出了各种药代动力学方法来解决姜黄素的生物利用度问题,如使用胡椒碱作为佐剂;还讨论了基于纳米技术的姜黄素制剂利用姜黄素类似物。