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Related Concept Videos

Regulation of Angiogenesis and Blood Supply01:24

Regulation of Angiogenesis and Blood Supply

Rapidly dividing tumors, embryos, and wounded tissues require more oxygen than usual, lowering the oxygen concentration in the blood. At low oxygen or hypoxic conditions, an oxygen-sensitive transcription factor called the hypoxia-inducible factor 1 or HIF1 is activated. HIF1 is a dimeric protein of alpha (ɑ) and beta (β) subunits.  Under optimal oxygen conditions, HIF1β is present in the nucleus while HIF1ɑ remains in the cytosol. HIF1ɑ is hydroxylated by prolyl hydroxylase and factor...
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Microorganisms exhibit diverse oxygen requirements and growth patterns driven by their metabolic strategies and environmental adaptations. Oxygen, while essential for many organisms, can also be toxic under certain conditions, shaping how microorganisms grow and survive.Oxygen Requirements of MicroorganismsMicroorganisms are classified based on their ability to use or tolerate oxygen:● Obligate aerobes like Mycobacterium tuberculosis need oxygen for energy production, as it serves as the...
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.
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The Tumor Microenvironment02:17

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Every normal cell or tissue is embedded in a complex local environment called stroma, consisting of different cell types, a basal membrane, and blood vessels. As normal cells mutate and develop into cancer cells, their local environment also changes to allow cancer progression. The tumor microenvironment (TME) consists of a complex cellular matrix of stromal cells and the developing tumor. The cross-talk between cancer cells and surrounding stromal cells is critical to disrupt normal tissue...
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Cancers arise due to mutations in genes involved in the regulation of cell division, which leads to unrestricted cell proliferation. Modern science and medicine have made great strides in the understanding and treatment of cancer, including eradicating cancer in some patients. However, there is still no cure for cancer. This is largely due to the fact that cancer is a large group of many diseases.

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Related Experiment Video

Updated: Jun 1, 2026

Anaerobic Growth and Maintenance of Mammalian Cell Lines
07:15

Anaerobic Growth and Maintenance of Mammalian Cell Lines

Published on: July 21, 2018

Ambient oxygen promotes tumorigenesis.

Ho Joong Sung1, Wenzhe Ma, Matthew F Starost

  • 1Center for Molecular Medicine, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, United States of America.

Plos One
|May 19, 2011
PubMed
Summary

Reducing oxygen exposure significantly increased tumor-free survival in mice by decreasing DNA damage and RAG recombinase levels, highlighting oxygen's role in genomic instability and cancer development.

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Tumor Hypoxia Assessment: In Vivo 3D Oxygen Imaging Through Electron Paramagnetic Resonance
07:07

Tumor Hypoxia Assessment: In Vivo 3D Oxygen Imaging Through Electron Paramagnetic Resonance

Published on: February 14, 2025

Area of Science:

  • Oncology
  • Genetics
  • Molecular Biology

Background:

  • Oxygen is a known mutagen and causes genomic instability in mammalian cells.
  • The effect of ambient oxygen on de novo tumorigenesis at the organismal level remains unclear.

Purpose of the Study:

  • To investigate the impact of ambient oxygen levels on de novo tumorigenesis in vivo.
  • To determine if reducing oxygen exposure can inhibit cancer development.

Main Methods:

  • Experiments were conducted using p53-/- mice, with varying ambient oxygen exposure.
  • Levels of oxidative DNA damage and RAG recombinase were measured in the thymus.
  • Two additional cancer models (APC tumor suppressor gene and chemical carcinogenesis) were used to assess oxygen's role.

Main Results:

  • Decreasing ambient oxygen exposure increased median tumor-free survival time by approximately 50% in p53-/- mice.
  • Reduced oxygen levels led to decreased oxidative DNA damage and RAG recombinase in the thymus.
  • Oxygen was associated with genomic instability in APC and chemical carcinogenesis models.

Conclusions:

  • Ambient oxygen plays a critical role in promoting de novo tumorigenesis and increasing genomic instability in vivo.
  • Modulating oxygen exposure may represent a novel therapeutic strategy for cancer prevention.