Review Article

Mitochondria-Targeted Antioxidants: A Step towards Disease Treatment

Table 5

MTAs in cancer models.

Mitochondria-targeted antioxidants/bioactive componentModels/clinical trialsDosageEffects/mechanismReference

SkQ1HT1080 cells40 nmol/L in culture medium(1) Suppressed cell growth and prolonged cell mitosis
(2) Induced distribution and activation of Aurora family kinases
[132]
Tumor cells in culture or mouse models40 nmol/L in culture medium; 250 nmol/(1) Decreased cell growth and the weight of subcutaneous tumors
(2) Prolonged cell mitosis and apoptosis
[132]
p53(-/-) mice5 nmol/ per day(1) Delayed appearance of tumors
(2) Inhibited the growth of xenografts tumors and angiogenesis
[133]
BALB/c mice in SPF environment1 and 30 nmol/ per day(1) Decreased the incidence of spontaneous cancers at the dosage of 30 nmol/
(2) Suppressed the cancer dissemination at 1 nmol/ dosage
[134]
Benzopyrene-induced carcinogenesis in SHR mice5 and 50 nmol/ per day(1) Inhibited tumor growth
(2) Dose-dependent effects were observed
[135]

KRSHHeLa and MCF-7 cells50 nmol/L in culture medium(1) Inhibited greater tumor cell growth than the normal cells
(2) Increased apoptosis of HeLa and MCF-7 cells, but not of MCF10A cells
(3) Accumulated in mitochondria and increased mitochondrial depolarization
[136]

Mito-TEMPON-Nitrosodiethylamine-induced hepatocarcinogenesis in BALB/c mice0.1 mg/ weekly(1) Increased animal survival ratio and decreased tumor incidence and tumor multiplicity
(2) Rescued the gap junctions and gap junctional intercellular communication of tumor cells
[137]

Notes: HeLa cells: cervical cancer cell line taken from Henrietta Lacks; HT1080: human sarcoma cell line; MCF-7: breast cancer cell line that consisted of the acronym of Michigan Cancer Foundation-7; p53: tumor protein p53; SPF; specific pathogen free.