Table 1 Key metabolic enzymes or transporters whose transcriptional deregulation has been reported to alter the energetic metabolism.

From: A genetic toolkit for the analysis of metabolic changes in Drosophila provides new insights into metabolic responses to stress and malignant transformation

Protein

Role in the energetic metabolism

Alterations reported in cancer contexts

References

GLUT1

Glucose transport through plasma membrane

Activation of isoforms 1 and 3 in mammalian tumor models.

Its silencing, concomitant with LDH, reduces the tumor phenotype observed upon Notch activation in Drosophila imaginal discs

34,38

Pyruvate Kinase (PK)

Conversion of Phosphoenolpyruvate into pyruvate

Increase of a PKM2 isoform in several mammalian tumor models

39,40

Mitochondrial Pyruvate Carrier (MPC)

Mitochondrial transporters of pyruvate

Inhibition of isoforms 1 and 2 in mammalian tumor models.

Its silencing in Drosophila leads to larval lethality when development occurs in media lacking a carbon source other than sucrose

41,42

Monocarboxylate Transporter (MCT)/Silnoon and Chaski

Transporters of lactate and pyruvate in the plasma membrane

Heightened expression of isoform 4 in mammalian tumor models

43

Pyruvate Dehydrogenase Kinase (PDHK)

Inhibition of the Pyruvate Dehydrogenase complex

Increase in Isoform 1 in several mammalian tumor models

44,45

Lactate Dehydrogenase (LDH)/Impl3

Reduction of pyruvate and lactate synthesis

Increase in LDHA isoform in several mammalian tumor models

Transformation from hyperplasia to neoplasia depends on LDH activity

37,46

  1. The table summarizes the physiological role of each of the genes in metabolism as well as the nature of the alteration in tumorigenesis.