Table 1.
Enzymes | Cancer-related alterations | Refs. |
---|---|---|
Cysteine dioxygenase (CDO) | ||
↑ CDO: | ||
- Good prognosis | 70 | |
- Bad prognosis | 76 | |
- ROS production | 71 | |
- Toxicity | 70 | |
- ↓ OXPHOS | 76 | |
- Ferroptosis inhibition | 75 | |
↓ CDO: | ||
- Poor prognosis | 71,74 | |
- Drug resistance | 71 | |
Cystathionine β-synthase (CBS) | ||
↑ CBS: | ||
- Cancer malignancy | 58,60,56-61 | |
- ↓ ROS production | 58,109,153 | |
- ↑ OXPHOS | 58,109,153 | |
- ↑ Proliferation | 170 | |
- ↑ Migration | 170 | |
- ↑ Angiogenesis | 156-159 | |
- Ferroptosis inhibition | 85,171 | |
Cystathionine γ-lyase (CSE) | ||
↑ CSE: | ||
- Cancer malignancy | 54,55,57,59,61 | |
- ↑ Angiogenesis | 156-159 | |
- Apoptosis inhibition | 168 | |
3-Mercaptopyruvate sulphurtransferase (3-MST) | ||
↑ 3-MST: | ||
- Cancer malignancy | 57,59,61 | |
- ↑ OXPHOS | 114,147,148 | |
Cysteine desulphurase (NFS1) | ||
↑ NFS1: | ||
- Ferroptosis inhibition | 138,140 | |
↓ NFS1: | ||
- Chemoresistance | 138 | |
Sulphide:quinone oxidoreductase (SQR) | ||
↑ SQR: | ||
- Hypoxia related | 154 | |
↓ SQR: | ||
- ↓ OXPHOS | 114,148 | |
Transporters | Cancer-related alterations | Refs. |
Alanine-serine-cysteine transporters 1 (ASCT1; SLC1A4) | ||
↑ ASCT1: | ||
- Cancer malignancy | 35,38,39,41-43 | |
- ↑ Glutamine metabolism | 41-43 | |
Alanine-serine-cysteine transporters 2 (ASCT2; SLC1A5) | ||
↑ ASCT2: | ||
- Cancer malignancy | 35,38,39,41-43 | |
- ↑ Glutamine metabolism | 41-43 | |
Excitatory amino acid transporter 3 (EAAT3; SLC1A1) | ||
↑ EAAT3: | ||
- Cancer malignancy | 35,38,39 | |
- Chemoresistance | 38 | |
Neutral and basic amino acid transporter (RBAT; SLC3A1) | ||
↑ RBAT: | ||
- ↓ ROS | 33 | |
- ↑ Cancer cell survival | 33 | |
xc− transport system (xCT; SLC7A11) | ||
↑ xCT: | ||
- Cancer malignancy | 25-27,180 | |
- Chemoresistance | 7,236 | |
- ↓ ROS | 7 | |
- Ferroptosis inhibition | 217,218,221 | |
↓ xCT: | ||
- TSP activation | 29,32 |
Presentation of the association between the expression and activity of enzymes and transporters and cancer metabolic alterations and disease progression.