Natural Agents Modulating Ferroptosis in Cancer: Molecular Pathways and Therapeutic Perspectives

Md Al Amin1, Mehrukh Zehravi2, Sherouk Hussein Sweilam3,4

  • 1Department of Pharmacy, Faculty of Health and Life Sciences, Daffodil International University, Dhaka, Bangladesh.

Insights

Natural compounds can induce ferroptosis, a form of cell death, offering new cancer treatments. These compounds show promise for combination therapy, enhancing efficacy and overcoming resistance in cancer cells.

Area of Science:

  • Biochemistry
  • Molecular Biology
  • Pharmacology

Background:

  • Ferroptosis is an iron-dependent cell death pathway implicated in cancer.
  • Cancer cells often develop resistance to conventional therapies.
  • Natural compounds offer potential therapeutic avenues due to their unique mechanisms.

Purpose of the Study:

  • To review the molecular mechanisms of natural compounds targeting ferroptosis in cancer.
  • To explore the potential of these compounds in combination therapies.
  • To discuss translational challenges and future clinical applications.

Main Methods:

  • Literature review of studies on natural compounds and ferroptosis.
  • Analysis of signaling pathways (Nrf2/Keap1, p53, GPX4) involved in ferroptosis.
  • Examination of synergistic effects with conventional cancer treatments.

Main Results:

  • Natural compounds (polyphenols, flavonoids, terpenoids, alkaloids) modulate ferroptosis.
  • These compounds exhibit tumor-specific selectivity and reduce systemic toxicity.
  • Combination therapy with natural compounds enhances efficacy and overcomes drug resistance.

Conclusions:

  • Natural compounds targeting ferroptosis present a promising strategy for novel cancer treatments, especially for resistant cancers.
  • Further research and clinical trials are essential to validate safety, bioavailability, and efficacy.
  • Optimized formulations and delivery methods are crucial for clinical translation.

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...
8.6K
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...
2.6K
Necrosis01:16

Necrosis

Necrosis is considered as an “accidental” or unexpected form of cell death that ends in cell lysis. The first noticeable mention of “necrosis” was in 1859 when Rudolf Virchow used this term to describe advanced tissue breakdown in his compilation titled “Cell Pathology”.
Morphological Manifestations of Necrosis
Necrotic cells show different types of morphological appearance depending on the type of tissue and infection. In coagulative necrosis, cells become...
6.3K
Cancer Therapies02:49

Cancer Therapies

Cancer therapies are various modes of treatment, such as surgery, radiation therapy, and chemotherapy that are administered to cancer patients.
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...
9.8K
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...
4.6K
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...
3.6K