Related Experiment Videos

Mammalian hexokinases and their abnormal expression in cancer

T A Smith1

  • 1Department of Nuclear Medicine, Royal Marsden Hospital, Sutton, Surrey, UK.

Insights

Hexokinases (HK) are key enzymes in glucose metabolism, crucial for cellular energy. Their altered activity and mitochondrial binding in tumors are linked to cancer progression and imaging applications.

Area of Science:

  • Biochemistry
  • Oncology
  • Cellular Metabolism

Background:

  • Hexokinases (HK) catalyze glucose phosphorylation, a vital metabolic step.
  • Four main hexokinase isoenzymes (HKI-IV) exist in mammalian tissues, with distinct molecular weights and tissue distributions.
  • HKI is predominant in the brain and associated with mitochondria, while HKIV (glucokinase) is specific to the liver and pancreas.

Purpose of the Study:

  • To review the role of hexokinases in cellular metabolism and their altered expression and activity in various cancers.
  • To explore the mechanisms behind changes in hexokinase activity in tumors, including gene dosage and mitochondrial binding.
  • To discuss the application of increased hexokinase activity in cancer imaging using (18F)fluoro-2-deoxy-D-glucose (FDG) and PET scans.

Main Methods:

  • Literature review of studies on hexokinase expression, activity, and function in normal and cancerous tissues.
  • Analysis of experimental data on hexokinase isoenzyme shifts and mitochondrial binding in tumor progression.
  • Examination of the principles behind FDG-PET imaging in relation to tumor glucose metabolism.

Main Results:

  • Increased hexokinase expression and activity are frequently observed in various cancers, correlating with tumor aggressiveness and metastatic potential.
  • Tumor cells exhibit altered hexokinase isoenzyme profiles and enhanced mitochondrial binding, contributing to increased glycolytic flux.
  • Specific mechanisms like gene dosage, altered transcription, and promoter activity modulation contribute to elevated hexokinase activity in tumors.
  • Conversely, some tumors, like gliomas, show decreased HK activity linked to specific gene losses.

Conclusions:

  • Hexokinases play a significant role in cancer metabolism, with dysregulation contributing to tumor growth and progression.
  • Understanding hexokinase alterations in tumors provides insights into cancer biology and potential therapeutic targets.
  • The increased glucose uptake and phosphorylation by tumor cells, mediated by hexokinases, form the basis for diagnostic imaging techniques like FDG-PET.

Related Concept Videos

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...
Abnormal Proliferation02:23

Abnormal Proliferation

Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the daughter...
Inhibition of Cdk Activity02:34

Inhibition of Cdk Activity

The orderly progression of the cell cycle depends on the activation of Cdk protein by binding to its cyclin partner. However, the cell cycle must be restricted when undergoing abnormal changes. Most cancers correlate to the deregulated cell cycle, and since Cdks are a central component of the cell cycle, Cdk inhibitors are extensively studied to develop anticancer agents. For instance, cyclin D associates with several Cdks, such as Cdk 4/6, to form an active complex. The cyclin D-Cdk4/6 complex...
PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a rapamycin-insensitive companion...
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,...
Cancer-Critical Genes II: Tumor Suppressor Genes01:05

Cancer-Critical Genes II: Tumor Suppressor Genes

Genes usually encode proteins necessary for the proper functioning of a healthy cell. Mutations can often cause changes to the gene expression pattern, thereby altering the phenotype.
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...