» Articles » PMID: 37762572

Amygdalin As a Promising Anticancer Agent: Molecular Mechanisms and Future Perspectives for the Development of New Nanoformulations for Its Delivery

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2023 Sep 28
PMID 37762572
Authors
Affiliations
Soon will be listed here.
Abstract

Cancer rates are increasing, and cancer is one of the main causes of death worldwide. Amygdalin, also known as vitamin B17 (and laetrile, a synthetic compound), is a cyanogenic glycoside compound that is mainly found in the kernels and pulps of fruits. This compound has been proposed for decades as a promising naturally occurring substance which may provide anticancer effects. This is a comprehensive review which critically summarizes and scrutinizes the available studies exploring the anticancer effect of amygdalin, highlighting its potential anticancer molecular mechanisms as well as the need for a nontoxic formulation of this substance. In-depth research was performed using the most accurate scientific databases, e.g., PubMed, Cochrane, Embase, Medline, Scopus, and Web of Science, applying effective, characteristic, and relevant keywords. There are several pieces of evidence to support the idea that amygdalin can exert anticancer effects against lung, breast, prostate, colorectal, cervical, and gastrointestinal cancers. Amygdalin has been reported to induce apoptosis of cancer cells, inhibiting cancer cells' proliferation and slowing down tumor metastatic spread. However, only a few studies have been performed in in vivo animal models, while clinical studies remain even more scarce. The current evidence cannot support a recommendation of the use of nutritional supplements with amygdalin due to its cyano-moiety which exerts adverse side effects. Preliminary data have shown that the use of nanoparticles may be a promising alternative to enhance the anticancer effects of amygdalin while simultaneously reducing its adverse side effects. Amygdalin seems to be a promising naturally occurring agent against cancer disease development and progression. However, there is a strong demand for in vivo animal studies as well as human clinical studies to explore the potential prevention and/or treatment efficiency of amygdalin against cancer. Moreover, amygdalin could be used as a lead compound by effectively applying recent developments in drug discovery processes.

Citing Articles

Anthocyanins in Black Soybean Coats Promote Apoptosis in Hepatocellular Carcinoma Cells by Regulating the JAK2/STAT3 Pathway.

Li Y, Wang M, Bai J, Li X, Xiao S, Song L Int J Mol Sci. 2025; 26(3).

PMID: 39940837 PMC: 11817063. DOI: 10.3390/ijms26031070.


Growth of Renal Cancer Cell Lines Is Strongly Inhibited by Synergistic Activity of Low-Dosed Amygdalin and Sulforaphane.

Markowitsch S, Pham T, Rutz J, Chun F, Haferkamp A, Tsaur I Nutrients. 2024; 16(21).

PMID: 39519581 PMC: 11547972. DOI: 10.3390/nu16213750.


Combined metabolomics and bioactivity assays kernelby-productsof two native Chinese cherry species: The sources of bioactive nutraceutical compounds.

Wang Z, Li L, Han J, Bai X, Wei B, Fan R Food Chem X. 2024; 23:101625.

PMID: 39100251 PMC: 11296007. DOI: 10.1016/j.fochx.2024.101625.


Survey of Physicians and Healers Using Amygdalin to Treat Cancer Patients.

Markowitsch S, Binali S, Rutz J, Chun F, Haferkamp A, Tsaur I Nutrients. 2024; 16(13).

PMID: 38999817 PMC: 11243289. DOI: 10.3390/nu16132068.

References
1.
Makarevic J, Rutz J, Juengel E, Kaulfuss S, Reiter M, Tsaur I . Amygdalin blocks bladder cancer cell growth in vitro by diminishing cyclin A and cdk2. PLoS One. 2014; 9(8):e105590. PMC: 4138189. DOI: 10.1371/journal.pone.0105590. View

2.
Abo El-Ela F, Gamal A, Elbanna H, Elbanna A, Salem H, Tulbah A . In Vitro and In Vivo Evaluation of the Effectiveness and Safety of Amygdalin as a Cancer Therapy. Pharmaceuticals (Basel). 2022; 15(11). PMC: 9697812. DOI: 10.3390/ph15111306. View

3.
Newmark J, Brady R, Grimley P, GAL A, Waller S, Thistlethwaite J . Amygdalin (Laetrile) and prunasin beta-glucosidases: distribution in germ-free rat and in human tumor tissue. Proc Natl Acad Sci U S A. 1981; 78(10):6513-6. PMC: 349070. DOI: 10.1073/pnas.78.10.6513. View

4.
El-Desouky M, Fahmi A, Nasraldin K . The Postulated Mechanism of Action of Amygdalin (Vitamin B17) on Cancer Cells. Anticancer Agents Med Chem. 2022; 23(8):894-899. DOI: 10.2174/1871520623666221124143751. View

5.
Shively R, Harding S, Hoffman R, Hill A, Astua A, Manini A . Rebound metabolic acidosis following intentional amygdalin supplement overdose. Clin Toxicol (Phila). 2019; 58(4):290-293. DOI: 10.1080/15563650.2019.1640369. View