Glossary

AND-Gate

Logic of an AND-gate

The AND gate is a basic digital logic gate that implements logical conjunction - it behaves according to the truth table to the right. A high output results only if both the inputs to the AND gate are high. If neither or only one input to the AND gate is high, a low output results.

Circulating Tumor Cell (CTC)

CTCs are thought to originate from the primary tumor from which they escape and colonize new tissues which they reach by traveling in the blood stream. They are believed to be the cause of metastasis. Therefore, they can be used as an early marker for metastatic cancer [Cáceres, 2015]. CTCs can be detected in the blood before the formation of metastasis, therefore allowing early intervention. However, CTCs are very scarce and detection methods have to be accordingly sensitive.

Epithelial-mesenchymal transition

The Epithelial-mesenchymal tenasition (EMT) takes place when epithelial cells detach from the wall of blood or lymphatic vessels and enter the circulatory system. These cells develop into multipotent stromal cells during normal embryonal development. However, a similar process occurs when cancerous cells invade the circulatory system to spread all over the body [Kalluri, 2009].

Fold-change sensor

Concept of fold-change sensor. Scheme from [Goentoro 2009]

A fold-change sensor generates a response to fold-changes in inputs levels, rather than in absolute values. The system is based on an incoherent feed-forward loop. An incoherent feed-forward loop is a system in which the intermediate pathways have opposite functional roles (i.e. at least one activation and one inhibition) , leading to the adaptation of the output. The delay introduced by the additional step in one of the pathway generates a pulsed response. Below, you can see the different parameters that influence this response.

Incoherent feed-forward loop and fold-change sensor. Scheme from [Goentoro 2009]

LldPRD Operon

LldPRD is an operon in E. coli that is involved in lactate metabolism [Aguilera, 2008]. It consists of a promotor region followed by three genes:

LldP

L-lactate Permease, a membrane transporter which partcipates in the active transport of L-Lactate, D-lactate and glycolate by using a proton force [Nunez, 2002].

LldR

L-lactate Regulator, a transcription factor that is responsive to L-lactate. In the absence of lactate it localizes to the operator regions O1/O2 and gene transcription is blocked. When lactate binds to LldR it detaches from the promotor region and gene expression is activated.

LldD

L-lactate Dehydrogenase, an enzyme that metabolizes L-lactate. Its expression is controlled by LldR acting on the upstream promoter. Replace this gene with any gene you want to upregulate in response to lactate.

Michaelis-Menten Kinetics

This is a basic model to describe the rate of a (potentially reversible) enzymatic reaction like the following:

Enzyme E binds to Substrate S and converts it into product P. Each conversion happens at a given rate characterized by the rate constants k. The rate at which product P is formed is given by:

The reaction rate v is the change in product concentration [P] over time. It increases with increasing substrate concentration [S].

The maximum rate V_max is reached when every Enzyme E is in action and working on a Substrate molecule S. It is therefore proportional to the enzyme concentration [E]₀ and determined by the turnover number k_cat, which describes the "work enthusiasm" of the enzyme and can vary greatly depending on the enzyme at hand. In mathematical terms this is represented by V_max = k_cat[E]₀.

K_M (called Michaelis constant) is the substrate concentration at which the reaction rate has reached half the maximum rate V_max. It measures the affinity of an enzyme to the substrate. The lower K_M (the quicker the half-maximum rate is reached) the higher the affinity. This measure can vary greatly as well.

Quorum sensing

Quorum sensing is a system by which bacteria "sense each other". This cell to cell communication is mediated by chemical signals such as AHL (N-acyl-L-homoserine lactone). This is a means to tune gene expression depending on the density of the population [Miller, 2001]. LuxR is the transcription factor that mediates the quorum sensing response. If AHL is present at sufficient concentrations it binds and activates LuxR, whereupon downstream gene expression is induced. Gene expression might become leaky if too much AHL accumulates over time. We therefore introduced a constitutively expressed AHL-Lactonase (AiiA) to degrade AHL and keep the concentration low.

TRAIL

The Tumor Necrosis Factor Related Apoptosis Inducing Ligand, TRAIL, is an important protein of our immune system which induces apoptosis in cells expressing the required death receptors, DR4 and DR5, thereby inactivating the target cell. Binding of TRAIL to DR4 or DR5 on the surface of a target cell leads to Caspase-8 dependent induction of apoptosis. Cancer cells often express elevated levels of the DR4 and DR5 death receptors and are therefore especially susceptible to treatment with TRAIL, whereas healthy cells are generally not harmed by TRAIL. In nature, TRAIL exists as a membrane-bound and a soluble version. In our system we are using the soluble form, referred to as sTRAIL [Johnstone, 2008].

Warburg Effect

Malignant tumors often tune their metabolism towards highly elevated rates of glycolysis, followed by lactic acid fermentation, rather than pyruvate hydrolysis in mitochondria. This gives the tumor cells a comparative advantage over normal cells due to the rapid intake of glucose for which the cells are competing. This effect is referred to as the Warburg effect since it was first described by Otto Warburg. It is not clear what the ultimate cause of this effect is. The transition to lactic acid fermentation occurs also in environments plenty of oxygen, and once it occurred, tumor cells keep this feature even in transition to metastasis [Vander Heiden et al, 2009].

Figure 5. Warburg effect scheme. Image from Vander Heiden, 2009