Table 2.
Description of the five types of drugs used when treating cancerous agents.
Drug | Treated Condition | CIPN Pathogenesis |
---|---|---|
Platinum Compounds | Tumors in cranium, digestive, urinary, respiratory, and reproductive systems. | Mitochondrial dysfunction. Increased oxidative stress. Voltage-gated K+ and Na+ hyperactivity. |
Taxanes | Tumors in breast, ovaries, prostate, lungs, and bladder. | Mitochondrial dysfunction. Increased oxidative stress. Voltage-gated K+ and Na+ hyperactivity. Altered functionality of skin-based receptors (Aβ, C, and Aδ nerve fibers). |
Vinca Alkaloids | Tumors in kidneys, liver, lungs, breast, and brain. Hematological malignancies, testicular, and non-small cell lung cancer. | Mitochondrial dysfunction. Microtubule function inhibition. |
Immunomodulators | Example: thalidomide. MM, glioblastoma, breast, and prostate cancer. | Inhibition of growth factors (VEGF, TNF-α, NF-kB, b-FGF). ROS activation. Induced hypoxia and ischemia. |
Proteosome Inhibitors | Example: bortezomib. Progressive, relapsed, or refractory MM. | Mitochondrial dysfunction. Increased oxidative stress. Increased apoptosis via release of Ca2+ in endoplasmic reticulum. |