Abstract

The Pentose Phosphate Pathway (PPP) is one of the key metabolic pathways occurring in living cells to produce energy and maintain cellular homeostasis. Cancer cells have higher cytoplasmic utilization of glucose (glycolysis), even in the presence of oxygen; this is known as the “Warburg Effect”. However, cytoplasmic glucose utilization can also occur in cancer through the PPP. This pathway contributes to cancer cells by operating in many different ways: (i) as a defense mechanism via the reduced form of nicotinamide adenine dinucleotide phosphate (NADPH) to prevent apoptosis, (ii) as a provision for the maintenance of energy by intermediate glycolysis, (iii) by increasing genomic material to the cellular pool of nucleic acid bases, (iv) by promoting survival through increasing glycolysis, and so increasing acid production, and (v) by inducing cellular proliferation by the synthesis of nucleic acid, fatty acid, and amino acid. Each step of the PPP can be upregulated in some types of cancer but not in others. An interesting aspect of this metabolic pathway is the shared regulation of the glycolytic and PPP pathways by intracellular pH (pHi). Indeed, as with glycolysis, the optimum activity of the enzymes driving the PPP occurs at an alkaline pHi, which is compatible with the cytoplasmic pH of cancer cells. Here, we outline each step of the PPP and discuss its possible correlation with cancer.

Highlights

  • In 1935 and 1936, Otto Warburg showed that pyridine nucleotide diphosphopyridine nucleotideDPN functioned as an electron carrier [1,2,3]

  • In the 1920s, Otto Warburg observed that cancer cells had a higher fermentation rate, and later concluded that cancer relied on the cytoplasmic utilization of glucose rather than mitochondrial utilization

  • Cytoplasmic utilization can occur through glycolysis and/or the Phosphate Pathway (PPP)

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Summary

Introduction

In 1935 and 1936, Otto Warburg showed that pyridine nucleotide diphosphopyridine nucleotide. DPN (currently known as NAD+ ) functioned as an electron carrier [1,2,3] He demonstrated the presence of a second enzyme called triphosphopyridine (TPN), currently known as NAP+. He discovered the Zwischenferment enzyme (known as glucose-6-phosphate dehydrogenase (G6PDH)) [1,2]. The PPP has been termed the phosphogluconate pathway or the hexose monophosphate shunt. It is a cytoplasmic pathway consisting of two phases: (i) the oxidative phase, followed by (ii) the nonoxidative phase.

Oxidative
Second Step
Third Step
Ribose-5 Phosphate Formation
Xylulose 5-Phosphate Formation
Fifth Step
Sixth Step
Seventh Step
NADPH and GSH
TheReactive
Concluding Remarks
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