Pentacyclic triterpenes of the lupane, oleanane and ursane group as tools in cancer therapy

Melanie N Laszczyk1

  • 1Betulin Institut, 64297 Darmstadt, Germany. m.laszczyk@betulin-institut.de

Planta Medica
|September 11, 2009
PubMed

Insights

Pentacyclic triterpenes from plants show promise for cancer treatment by targeting multiple pathways, including apoptosis, angiogenesis, and inflammation. Further research is needed to confirm their clinical efficacy as novel anticancer agents.

Area of Science:

  • Phytochemistry
  • Pharmacology
  • Oncology

Background:

  • Modern cancer therapy extends beyond direct cancer cell elimination.
  • Targeting the tumor microenvironment, angiogenesis, immune response, and inflammation are emerging strategies.
  • Plant-derived compounds, particularly pentacyclic triterpenes, offer multifaceted therapeutic potential.

Purpose of the Study:

  • To review the anticancer potential of lupane, oleanane, and ursane triterpenes.
  • To summarize their diverse mechanisms of action in cancer treatment.
  • To highlight their relevance in the context of novel cancer therapy strategies.

Main Methods:

  • Literature review of studies on triterpenes and their anticancer effects.
  • Focus on apoptosis induction, antiangiogenesis, differentiation induction, anti-inflammatory, immune modulation, and antioxidative properties.
  • Analysis of triterpenes from plant sources like birch bark and rosemary.

Main Results:

  • Betulinic acid and other triterpenes induce apoptosis in various cancer cell lines (melanoma, breast, colon, lung, neuroblastoma).
  • Triterpenes exhibit antiangiogenic, differentiation-inducing, anti-inflammatory, immune-modulating, and antioxidative effects.
  • Lupane-type triterpenes (betulin, betulinic acid, lupeol) show significant anti-inflammatory and immune-modulating activities.

Conclusions:

  • Pentacyclic triterpenes possess multitarget potential for cancer therapy.
  • Their diverse pharmacological activities align with new cancer treatment strategies.
  • While promising, clinical trials are needed to validate their efficacy in cancer treatment.

Related Concept Videos

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 specific...
Drugs that Stabilize Microtubules01:15

Drugs that Stabilize Microtubules

Microtubules are dynamic structures that undergo cycles of catastrophe and rescue. The microtubules play a central role in cell division by forming the spindle apparatus for segregating the chromosomes. This makes them ideal targets for regulating dividing cells in tumors and malignant cancer cells. Microtubule stabilizing drugs help stabilize the microtubule formation and promote its polymerization. Paclitaxel was the first microtubule stabilizing agent used as anticancer drug in chemotherapy...
Treatment Resistent Cancers02:56

Treatment Resistent Cancers

Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
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...
Drugs that Destabilize Microtubules01:10

Drugs that Destabilize Microtubules

Microtubules are dynamic structures and can be regulated by microtubule targeting agents (MTAs). Microtubule destabilizing drugs are a class of MTAs that destabilize and prevent microtubules' polymerization. Both natural and synthetic chemicals can be found under this class of drugs. Vincristine and vinblastine, two vinca alkaloids, and colchicine were among the first to be discovered. These drugs can affect cells in various ways, either by inducing a change in cell morphology, preventing...
Mouse Models of Cancer Study02:43

Mouse Models of Cancer Study

Mice have long served as models for studying human biology and pathology because of their phylogenetic and physiological similarity with humans. They are also easy to maintain and breed in the laboratory, and hence, many inbred strains are now available for research. Studies on mice have contributed immeasurably to our understanding of cancer biology.
The development of transgenic, knockout, and knock-in mice has led to an exponential increase in their use as model organisms in research,...