Anticancer Activity of Diosgenin and Its Molecular Mechanism

Qun-Li Ren1,2,3, Qian Wang1,2,3, Xin-Qun Zhang4

  • 1Special Key Laboratory of Microbial Resources and Drug Development, Higher Education Institution, Zunyi, Guizhou Province, 563000, China.

Insights

Diosgenin shows significant anticancer potential against various cancers by inhibiting tumor growth and promoting cell death. Further clinical trials are needed to optimize its application and bioavailability.

Area of Science:

  • Phytochemistry
  • Pharmacology
  • Oncology

Background:

  • Diosgenin, a natural steroidal sapogenin from plants like Trigonella foenum-graecum, is recognized for its therapeutic potential.
  • It has demonstrated activity against a wide spectrum of cancers, including oral, liver, lung, and prostate cancers.

Purpose of the Study:

  • To provide a comprehensive overview of diosgenin's anticancer effects based on in vivo, in vitro, and clinical research.
  • To explore strategies for enhancing diosgenin's biological activity and bioavailability.

Main Methods:

  • Review of preclinical (in vivo, in vitro) studies on diosgenin's mechanisms of action.
  • Analysis of clinical investigations assessing diosgenin's dosage and safety.
  • Examination of recent developments in diosgenin drug delivery and derivatives.

Main Results:

  • Preclinical data indicate diosgenin inhibits tumor proliferation, induces apoptosis and autophagy, and reduces metastasis.
  • Clinical studies suggest favorable dosage and safety profiles for diosgenin.
  • Development of nano-drug carriers, combination therapies, and derivatives aims to improve efficacy.

Conclusions:

  • Diosgenin exhibits broad-spectrum anticancer properties supported by preclinical and preliminary clinical evidence.
  • Further rigorous clinical trials are essential to address limitations and fully realize diosgenin's therapeutic potential in cancer treatment.

Related Concept Videos

Inhibition of Cdk Activity02:34

Inhibition of Cdk Activity

The orderly progression of the cell cycle depends on the activation of Cdk protein by binding to its cyclin partner. However, the cell cycle must be restricted when undergoing abnormal changes. Most cancers correlate to the deregulated cell cycle, and since Cdks are a central component of the cell cycle, Cdk inhibitors are extensively studied to develop anticancer agents. For instance, cyclin D associates with several Cdks, such as Cdk 4/6, to form an active complex. The cyclin D-Cdk4/6 complex...
4.8K
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
3.8K
Mechanism of Angiogenesis01:10

Mechanism of Angiogenesis

Blood vessel formation starts early during embryonic development, around day 7. In the extraembryonic yolk sac, mesodermal precursor cells called hemangioblast proliferate and differentiate into angioblast. Angioblasts express vascular endothelial growth factor receptor 2 or VEGFR2, which binds VEGF-A, a proangiogenic factor, guiding blood vessel formation. VEGF signaling promotes angioblasts to form a blood island in the developing embryo. Angioblasts further differentiate, giving rise to...
5.7K
Diels–Alder Reaction: Characteristics of Dienes01:29

Diels–Alder Reaction: Characteristics of Dienes

The Diels–Alder reaction brings together a diene and a dienophile to form a six-membered ring. Both components have unique characteristics that influence the rate of the reaction.
Characteristics of the diene
Conformation
The simplest example of a diene is 1,3-butadiene, an acyclic conjugated π system. At room temperature, the molecule exists as a mixture of s-cis and s-trans conformers by virtue of rotation around the carbon–carbon single bond. Although the s-trans isomer is...
4.2K
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
7.8K
Mutagenicity and Carcinogenicity01:25

Mutagenicity and Carcinogenicity

Mutagenicity and carcinogenicity refer to the ability of drugs to cause genetic defects and induce cancer, respectively. The International Agency for Research on Cancer (IARC) classifies agents into four groups based on their carcinogenic potential. Group 1 agents are known human carcinogens; group 2A agents are probably carcinogenic to humans; group 3 agents lack data to support their role in carcinogenesis; and group 4 includes agents for which data support that they are not likely to be...
1.3K