ROS-modulated therapeutic approaches in cancer treatment

Muhammad Hassan Raza1, Sami Siraj2, Abida Arshad3

  • 1Department of Bioinformatics and Biotechnology, International Islamic University, Sector H-10, Islamabad, 44000, Pakistan. Hassan.bsbt755@iiu.edu.pk.

Abstract

Insights

Cancer cells produce reactive oxygen species (ROS), which can be targeted for therapy. Manipulating ROS levels offers a promising strategy for selective cancer treatment, with human microbiota influencing treatment response.

Area of Science:

  • Biochemistry
  • Oncology
  • Microbiology

Background:

  • Reactive oxygen species (ROS) are integral to cancer cell metabolism and survival.
  • Dysregulated ROS levels are a hallmark of cancer, influencing proliferation and therapeutic sensitivity.

Purpose of the Study:

  • To review the multifaceted role of ROS in cancer development and progression.
  • To explore ROS-mediated therapeutic strategies for selective cancer targeting.
  • To examine the influence of the human microbiota on ROS-dependent cancer therapy.

Main Methods:

  • Comprehensive literature search of PubMed, Web of Science, and Google Scholar.
  • Analysis of peer-reviewed articles, clinical studies, and reviews on ROS in biological systems.
  • Focus on ROS production, cancer roles, therapeutic strategies, and microbiota interactions.

Main Results:

  • Tumor oxidative stress and ROS adaptations are key features of cancer cells.
  • ROS-scavenging and ROS-boosting therapies demonstrate efficacy in preclinical and clinical settings.
  • The human microbiota significantly modulates cancer therapy outcomes.

Conclusions:

  • Cancer cells' altered redox homeostasis creates vulnerabilities exploitable by ROS-targeted therapies.
  • ROS-dependent therapeutic approaches, including scavenging and boosting, show significant promise.
  • Microbiota plays a critical role in modulating cancer therapy response and systemic functions.

Related Concept Videos

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...
10.3K
Treatment Resistant Cancers02:56

Treatment Resistant 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...
3.8K
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...
9.0K
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,...
7.2K
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...
4.9K