Vitamin C Inhibited Pulmonary Metastasis through Activating Nrf2/HO-1 Pathway.
Shuli ManJingxian BiFurui LiuWenwen XieLong MaPublished in: Molecular nutrition & food research (2024)
As an important nutritional component, vitamin C (Vc) shows good antitumor activity in a variety of cancer, but there are few studies in pulmonary metastasis. In order to verify its anticancer and antimetastatic effect, the study sets up H22 pulmonary metastasis mouse model. The results show that intraperitoneal injection of Vc inhibits pulmonary metastasis through up-regulating the expression of Nrf2, HO-1, cleaved caspases 3 and 9, and causing DNA damage and apoptosis which is similar to the pro-oxidant effect of Vc in p53 null cells (H1299 cells). Meanwhile, oral administration of Vc up-regulates the expression of p53, directly activates Nrf2/HO-1 pathway, increases expression of cleaved caspases 3 and 9, and ultimately inhibits pulmonary metastasis, which is the same as the antioxidant result of Vc in p53 wild-type cells. In addition, Vc inhibits the proliferation and migration of lung cancer cells in a concentration-dependent manner and has little cytotoxic effects on normal cells. Notably, the experiment further illustrates that besides intravenous Vc, oral Vc significantly inhibits the pulmonary metastasis in mice. All in all, these findings provide new clues for Vc-treated pulmonary metastasis in clinical research.
Keyphrases
- cell cycle arrest
- induced apoptosis
- pulmonary hypertension
- oxidative stress
- pi k akt
- dna damage
- poor prognosis
- endoplasmic reticulum stress
- cell death
- mouse model
- signaling pathway
- anti inflammatory
- type diabetes
- binding protein
- cell proliferation
- dna repair
- newly diagnosed
- long non coding rna
- skeletal muscle
- insulin resistance
- high dose
- lymph node metastasis
- squamous cell