» Articles » PMID: 38726411

Oridonin from : An Emerging Potential in Cancer Therapy - A Comprehensive Review

Abstract

Cancer incidences are rising each year. In 2020, approximately 20 million new cancer cases and 10 million cancer-related deaths were recorded. The World Health Organization (WHO) predicts that by 2024 the incidence of cancer will increase to 30.2 million individuals annually. Considering the invasive characteristics of its diagnostic procedures and therapeutic methods side effects, scientists are searching for different solutions, including using plant-derived bioactive compounds, that could reduce the probability of cancer occurrence and make its treatment more comfortable. In this regard, oridonin (ORI), an ent-kaurane diterpenoid, naturally found in the leaves of species, has been found to have antitumor, antiangiogenesis, antiasthmatic, antiinflammatory, and apoptosis induction properties. Extensive research has been performed on ORI to find various mechanisms involved in its anticancer activities. This review article provides an overview of ORI's effectiveness on murine and human cancer populations from 1976 to 2022 and provides insight into the future application of ORI in different cancer therapies.

Citing Articles

Enhancing cancer therapy: advanced nanovehicle delivery systems for oridonin.

Su Y, Liu L, Lin C, Deng D, Li Y, Huang M Front Pharmacol. 2024; 15:1476739.

PMID: 39691396 PMC: 11649421. DOI: 10.3389/fphar.2024.1476739.


Novel-and Not So Novel-Inhibitors of the Multifunctional CRM1 Protein.

Aumann W, Kazi R, Harrington A, Wechsler D Oncol Rev. 2024; 18:1427497.

PMID: 39161560 PMC: 11330842. DOI: 10.3389/or.2024.1427497.


Oridonin from : An emerging potential in cancer therapy - A comprehensive review.

Ali M, Khan N, Ali A, Akram H, Zafar N, Imran K Food Sci Nutr. 2024; 12(5):3046-3067.

PMID: 38726411 PMC: 11077219. DOI: 10.1002/fsn3.3986.

References
1.
Yi S, Chen Y, Wen L, Yang L, Cui G . Downregulation of nucleoporin 88 and 214 induced by oridonin may protect OCIM2 acute erythroleukemia cells from apoptosis through regulation of nucleocytoplasmic transport of NF-κB. Int J Mol Med. 2012; 30(4):877-83. DOI: 10.3892/ijmm.2012.1067. View

2.
Xue B, Wang Y, Tang X, Xie P, Wang Y, Luo F . Biodegradable self-assembled MPEG-PCL micelles for hydrophobic oridonin delivery in vitro. J Biomed Nanotechnol. 2012; 8(1):80-9. DOI: 10.1166/jbn.2012.1358. View

3.
Leng X, Huang H, Wang W, Sai N, You L, Yin X . Zirconium-Porphyrin PCN-222: pH-responsive Controlled Anticancer Drug Oridonin. Evid Based Complement Alternat Med. 2019; 2018:3249023. PMC: 6304552. DOI: 10.1155/2018/3249023. View

4.
Li D, Wu L, Tashiro S, Onodera S, Ikejima T . Oridonin inhibited the tyrosine kinase activity and induced apoptosis in human epidermoid carcinoma A431 cells. Biol Pharm Bull. 2007; 30(2):254-60. DOI: 10.1248/bpb.30.254. View

5.
Huang H, Weng H, Wang L, Yu C, Huang Q, Zhao P . Triggering Fbw7-mediated proteasomal degradation of c-Myc by oridonin induces cell growth inhibition and apoptosis. Mol Cancer Ther. 2012; 11(5):1155-65. DOI: 10.1158/1535-7163.MCT-12-0066. View