Boron- and phosphorus-containing molecular/nano platforms: exploiting pathological redox imbalance to fight cancer

Anna Wolfram1, Pablo Fuentes-Soriano1, Christel Herold-Mende2

  • 1Faculty of Pharmacy, University of Castilla-La Mancha Calle Almansa 14 - Edif. Bioincubadora, 02008, Albacete, Spain. carlos.romero.nieto@oci.uni-heidelberg.de.

Nanoscale
|November 3, 2022
PubMed

Insights

Boron and phosphorus compounds offer novel strategies to combat cancer by targeting cellular redox imbalance. These materials provide tunable platforms for developing innovative anticancer drugs with potential to reduce mortality.

Area of Science:

  • Oncology
  • Materials Science
  • Medicinal Chemistry

Background:

  • Cancer remains a leading global cause of death with persistent challenges in treatment efficacy and high recurrence rates.
  • Redox imbalance is a key characteristic of cancer cells that presents a potential therapeutic target.
  • Current anticancer therapies face limitations, necessitating the exploration of novel treatment modalities.

Purpose of the Study:

  • To review recent advancements in boron- and phosphorus-containing materials for anticancer drug design.
  • To highlight the potential of these materials in exploiting cancer cell redox imbalance.
  • To provide insights into methodologies for developing targeted cancer therapies.

Main Methods:

  • Review of recent literature on boron and phosphorus derivatives in cancer research.
  • Analysis of the chemical properties and tuneability of boron and phosphorus compounds.
  • Exploration of strategies for designing molecular and nano-platforms targeting cancer redox imbalance.

Main Results:

  • Boron and phosphorus derivatives offer unique chemical properties for drug design, including regioselectivity, tuneability, and stability.
  • These materials can be engineered into platforms to selectively target cancer cell redox imbalance, inducing necrosis or apoptosis.
  • The field is nascent but shows significant promise for developing novel anticancer agents.

Conclusions:

  • Boron- and phosphorus-based molecular/nano platforms represent a promising avenue for rational anticancer drug discovery.
  • Targeting cancer's redox imbalance with these materials offers a selective approach to treatment.
  • Further research and development in this area hold substantial potential for improving cancer therapy outcomes.

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...
7.8K
Electron Transport Chain: Complex I and II01:46

Electron Transport Chain: Complex I and II

The mitochondrial electron transport chain (ETC) is the main energy generation system in the eukaryotic cells. However, mitochondria also produce cytotoxic reactive oxygen species (ROS) due to the large electron flow during oxidative phosphorylation. While Complex I is one of the primary sources of superoxide radicals, ROS production by Complex II is uncommon and may only be observed in cancer cells with mutated complexes.
ROS generation is regulated and maintained at moderate levels necessary...
14.9K
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...
7.9K
Adaptive Mechanisms in Cancer Cells02:53

Adaptive Mechanisms in Cancer Cells

Cancer cells accumulate genetic changes at an abnormally rapid rate due to the defects in the DNA repair mechanisms. From an evolutionary perspective, such genetic instability is advantageous for cancer development. Mutant cell lines accumulate a series of beneficial mutations that contribute to their progression into cancer.
Some of the advantages that cancer cells have on normal cells include - enhanced ability to divide without terminally differentiating, induce new blood vessel formation,...
5.9K
Combination Therapies and Personalized Medicine02:50

Combination Therapies and Personalized Medicine

Combining two or more treatment methods increases the life span of cancer patients while reducing damage to vital organs or tissue from the overuse of a single treatment. Combination therapy also targets different cancer-inducing pathways, thus reducing the chances of developing resistance to treatment.
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...
5.0K
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...
2.1K