Chemopreventive and anti-angiogenic effects of dietary phenethyl isothiocyanate in an N-methyl nitrosourea-induced breast cancer animal model.

Chemopreventive and anti-angiogenic effects of dietary phenethyl isothiocyanate in an N-methyl nitrosourea-induced breast cancer animal model.
复制标题

DOI:
10.1002/bdd.1826
复制
发表时间:
2013-03
影响因子:
2.1
通讯作者:
Morris, Marilyn E.
Morris, Marilyn E.
中科院分区:
医学4区
文献类型:
--
作者:
Aras, Urvi;Gandhi, Yash A.;Masso-Welch, Patricia A.;Morris, Marilyn E.

文献摘要

参考文献

被引文献

相似文献

The effect of phenethyl isothiocyanate (PEITC), a component of cruciferous vegetables, on the initiation and progression of cancer was investigated in a chemically induced estrogen-dependent breast cancer model. Breast cancer was induced in female Sprague Dawley rats (8 weeks old) by the administration of N-methyl nitrosourea (NMU). Animals were administered 50 or 150 µmol/kg oral PEITC and monitored for tumor appearance for 18 weeks. The PEITC treatment prolonged the tumor-free survival time and decreased the tumor incidence and multiplicity. The time to the first palpable tumor was prolonged from 69 days in the control, to 84 and 88 days in the 50 and 150 µmol/kg PEITC-treated groups. The tumor incidence in the control, 50 µmol/kg, and 150 µmol/kg PEITC-treated groups was 56.6%, 25.0% and 17.2%, while the tumor multiplicity was 1.03, 0.25 and 0.21, respectively. Differences were statistically significant (p < 0.05) from the control, but there were no significant differences between the two dose levels. The intratumoral capillary density decreased from 4.21 ± 0.30 vessels per field in the controls to 2.46 ± 0.25 in the 50 µmol/kg and 2.36 ± 0.23 in the 150 µmol/kg PEITC-treated animals. These studies indicate that supplementation with PEITC prolongs the tumor-free survival, reduces tumor incidence and burden, and is chemoprotective in NMU-induced estrogen-dependent breast cancer in rats. For the first time, it is reported that PEITC has anti-angiogenic effects in a chemically induced breast cancer animal model, representing a potentially significant mechanism contributing to its chemopreventive activity.
DOI: 10.1016/j.canlet.2005.10.033
发表时间: 2006-10-08
期刊: CANCER LETTERS
影响因子: 9.7
作者:
Kijkuokool, Pisamai;Parhar, Ishwar S.;Malaivijitnond, Suchinda
通讯作者: Malaivijitnond, Suchinda
DOI: 10.3109/00498258309052256
发表时间: 1983-01-01
期刊: XENOBIOTICA
影响因子: 1.8
作者:
MENNICKE, WH;GORLER, K;KRUMBIEGEL, G
通讯作者: KRUMBIEGEL, G
DOI: 10.1093/carcin/bgi100
发表时间: 2005-08-01
期刊: CARCINOGENESIS
影响因子: 4.7
作者:
Chan, MM;Lu, X;Miron, PL
通讯作者: Miron, PL
DOI: 10.3892/ijo.2012.1335
发表时间: 2012-04
影响因子: 5.2
作者:
Hudson TS;Perkins SN;Hursting SD;Young HA;Kim YS;Wang TC;Wang TT
通讯作者: Wang TT
DOI: 10.3892/ijo.2011.1133
发表时间: 2011-11-01
影响因子: 5.2
作者:
Manni, Andrea;Richie, John P., Jr.;El-Bayoumy, Karam
通讯作者: El-Bayoumy, Karam