Difference between revisions of "Team:Freiburg/Tumor microenvironment"

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<p>Tumor microenvironment (TM) refers to the cellular environment surrounding a tumor, which includes blood vessels, normal cells and molecules. The interaction between a tumor and its microenvironment results in different physiological processes providing both beneficial and adverse consequences for tumorigenesis (Quail & Joyce, 2013).  
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<p>Tumor microenvironment (TM) refers to the cellular environment surrounding a tumor, which includes blood vessels, normal cells and molecules. The interaction between a tumor and its microenvironment results in different physiological processes providing both beneficial and adverse consequences for tumorigenesis (Quail & Joyce, 2013). Generally spoken, gene expression is altered in tumor cells leading to the secretion of various molecules such as cytokines, growth factors, and cellular components, for instance, exosomes to recruit stroma and vascular cells (Quail & Joyce, 2013; Mittal <i>et al.</i>, 2014). Various immune effector cells can also be found in tumor microenvironment, yet their anti-tumor functions are downregulated due to tumor-derived signals such as cytokines (Whiteside, 2008).There are several factors which are altered in comparison to the healthy interstitium. In the following we will highlight and describe some of the major factors.
 
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<p>Gene expression is altered in tumor cells to secrete molecules such as cytokines, growth factors, and cellular components, for instance, exosomes to recruit stroma and vascular cells (Quail & Joyce, 2013; Mittal <i>et al.</i>, 2014). Regardless of different tumor types and their tissue of origin there are some general hallmarks that govern tumorigenesis. Various immune effector cells can also be found in tumor microenvironment, yet their anti-tumor functions are downregulated due to tumor-derived signals such as cytokines (Whiteside, 2008).
 
  
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<p>Hypoxia is defined as the reduction or lack of oxygen in organs, tissues or cells (Yotnda <i>et al.</i>, 2011). Hypoxia  (<b>Fig. 1</b>) is a constantly evolving participant in overall tumor growth (Patel & Sant, 2016; Kim <i>et al.</i>, 2009) and remains the predominant regulator of angiogenesis in the tumor microenvironment (Mittal <i>et al.</i>, 2014). The actual physiological levels of oxygen level in healthy tissues ranges from 3-6 % (Tian & Bae, 2012), while that of tumors are approximately 1 % (McKeown, 2014), which can be an important factor to distinguish healthy tissues and tumors.  
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<p>One of the key characterisitics of tumors is their fast growth, which in turns leads to the a lac of oxygen, termed hypoxia(Yotnda <i>et al.</i>, 2011). Hypoxia  (<b>Fig. 1</b>) is a constantly evolving participant in overall tumor growth (Patel & Sant, 2016; Kim <i>et al.</i>, 2009) and remains the predominant regulator of angiogenesis in the tumor microenvironment (Mittal <i>et al.</i>, 2014). The actual physiological levels of oxygen level in healthy tissues ranges from 3-6 % (Tian & Bae, 2012), while that of tumors are approximately 1 % (McKeown, 2014), which can be an important factor to distinguish healthy tissues and tumors.  
 
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<p>Tumor angiogenesis is normally induced by a tumor to generate its dedicated blood supply for oxygen and other nutrients by secretion of various growth factors, including vascular endothelial growth factor (VEGF). VEGF (<b>Fig. 1</b>) promotes growth of blood vessels and is regarded as constituent element of the tumor microenvironment (Mittal <i>et al.</i>, 2014). The concentration of VEGF in tumor fluids of cancer patient ranges depending on tumor types from 1.7 pM to 320 pM (Finley & Popel, 2013).
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<p>To overcome this oxygen limitation, tumors typically induce angiogenesis to generate its dedicated blood supply for oxygen and other nutrients. To do so, it secretes various growth factors, including vascular endothelial growth factor (VEGF). VEGF (<b>Fig. 1</b>) promotes growth of blood vessels and is regarded as constituent element of the tumor microenvironment (Mittal <i>et al.</i>, 2014).
 
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<p>In addition, acidic extracellular pH  (<b>Fig. 1</b>) is a major feature of tumor tissue due to lactate secretion from anaerobic glycolysis and CO<sub>2</sub> from the pentose phosphate pathway (Kato <i>et al.</i>, 2013). Studies on different tumor nodules in human patient reveal an average extracellular pH of 7.0, in contrast to the physiological pH of 7.4 (Tian & Bae, 2012).  
 
<p>In addition, acidic extracellular pH  (<b>Fig. 1</b>) is a major feature of tumor tissue due to lactate secretion from anaerobic glycolysis and CO<sub>2</sub> from the pentose phosphate pathway (Kato <i>et al.</i>, 2013). Studies on different tumor nodules in human patient reveal an average extracellular pH of 7.0, in contrast to the physiological pH of 7.4 (Tian & Bae, 2012).  

Revision as of 21:38, 1 November 2017

Tumor Microenvironment


Tumor microenvironment (TM) refers to the cellular environment surrounding a tumor, which includes blood vessels, normal cells and molecules. The interaction between a tumor and its microenvironment results in different physiological processes providing both beneficial and adverse consequences for tumorigenesis (Quail & Joyce, 2013). Generally spoken, gene expression is altered in tumor cells leading to the secretion of various molecules such as cytokines, growth factors, and cellular components, for instance, exosomes to recruit stroma and vascular cells (Quail & Joyce, 2013; Mittal et al., 2014). Various immune effector cells can also be found in tumor microenvironment, yet their anti-tumor functions are downregulated due to tumor-derived signals such as cytokines (Whiteside, 2008).There are several factors which are altered in comparison to the healthy interstitium. In the following we will highlight and describe some of the major factors.

Tumor Microenvironment

Figure 1: Tumor Microenvironment
In the tumor microenvironment the levels of VEGF (vascular endothelial growth factor) are increased, while the extracellular pH as well as the oxygen concentration decrease, which creates an acidic and hypoxic environment.

One of the key characterisitics of tumors is their fast growth, which in turns leads to the a lac of oxygen, termed hypoxia(Yotnda et al., 2011). Hypoxia (Fig. 1) is a constantly evolving participant in overall tumor growth (Patel & Sant, 2016; Kim et al., 2009) and remains the predominant regulator of angiogenesis in the tumor microenvironment (Mittal et al., 2014). The actual physiological levels of oxygen level in healthy tissues ranges from 3-6 % (Tian & Bae, 2012), while that of tumors are approximately 1 % (McKeown, 2014), which can be an important factor to distinguish healthy tissues and tumors.

To overcome this oxygen limitation, tumors typically induce angiogenesis to generate its dedicated blood supply for oxygen and other nutrients. To do so, it secretes various growth factors, including vascular endothelial growth factor (VEGF). VEGF (Fig. 1) promotes growth of blood vessels and is regarded as constituent element of the tumor microenvironment (Mittal et al., 2014).

In addition, acidic extracellular pH (Fig. 1) is a major feature of tumor tissue due to lactate secretion from anaerobic glycolysis and CO2 from the pentose phosphate pathway (Kato et al., 2013). Studies on different tumor nodules in human patient reveal an average extracellular pH of 7.0, in contrast to the physiological pH of 7.4 (Tian & Bae, 2012).

Those factors that determine the nature of the tumor are considered by most therapeutic approaches to develop targeted therapies. Hypoxia, low pH and VEGF are three common characteristics of the tumor microenvironment. Therefore we chose these conditions to control the expression of chimeric antigen receptor (CAR) in T cells by an AND gate.