δ-Tocotrienol is the Most Potent Vitamin E Form in Inhibiting Prostate Cancer Cell Growth and Inhibits Prostate Carcinogenesis in Ptenp-/- Mice.

δ-Tocotrienol is the Most Potent Vitamin E Form in Inhibiting Prostate Cancer Cell Growth and Inhibits Prostate Carcinogenesis in Ptenp-/- Mice.
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DOI:
10.1158/1940-6207.capr-21-0508
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发表时间:
2022-04-01
期刊:
Cancer prevention research (Philadelphia, Pa.)
影响因子:
--
通讯作者:
Yang CS
Yang CS
中科院分区:
其他
文献类型:
--
作者:
Wang H;Yan W;Sun Y;Yang CS

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Vitamin E compounds, consisting of α, β, γ, and δ forms of tocopherols and tocotrienols, display different cancer preventive activities in experimental models. Tocotrienols may have higher potential for clinical use due to their lower effective doses in laboratory studies. However, most studies on tocotrienols have been carried out using cancer cell lines. Strong data from animal studies may encourage the use of tocotrienols for human cancer prevention research. To examine the cancer inhibitory activity of different vitamin E forms, we first investigated their inhibitory activities of different vitamin E forms in prostate cancer cell lines. We found that δ-tocotrienol (δT3) was the most effective form in inhibiting cell growth at equivalent doses. Because of this in vitro potency, δT3 was further studied using prostate specific Pten−/− (Ptenp−/−) mice. We found that 0.05% δT3 in diet reduced prostate adenocarcinoma multiplicity by 32.7%, featuring increased apoptosis and reduced cell proliferation. The inhibitory effect of 0.05% δT3 in diet was similar to that of 0.2% δ-tocopherol (δT) in diet reported previously. Our further study on the δT3-induced transcriptome changes indicated that δT3 inhibited genes in blood vessel development in the prostate of Ptenp−/− mice, which was confirmed by immunohistochemistry. Together, our results demonstrate that δT3 effectively inhibits the development of prostate adenocarcinoma in Ptenp−/− mice, which involves inhibition of proliferation and angiogenesis and promotion of apoptosis.
DOI: 10.1371/journal.pone.0040204
发表时间: 2012
期刊: PloS one
影响因子: 3.7
作者:
Weinstein SJ;Peters U;Ahn J;Friesen MD;Riboli E;Hayes RB;Albanes D
通讯作者: Albanes D