2009
DOI: 10.1016/j.jsbmb.2008.11.002
|View full text |Cite|
|
Sign up to set email alerts
|

Combination of 2-methoxyestradiol (2-ME2) and eugenol for apoptosis induction synergistically in androgen independent prostate cancer cells

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
32
0

Year Published

2010
2010
2023
2023

Publication Types

Select...
6
2

Relationship

0
8

Authors

Journals

citations
Cited by 54 publications
(33 citation statements)
references
References 33 publications
1
32
0
Order By: Relevance
“…67 Supporting the suggestion that the genotoxicity of estrogen metabolites is involved in prostate carcinogenesis is the observation of increased DNA strand breakage 52 and nuclear staining of 8-hydroxy-2′-deoxy-guanosine 60 in the prostates of rats treated with T plus E2. Conversely, increased expression or activity of COMT was shown to protect against estrogen-induced cancer by mediating the conversion of catechol estrogens into methoxyestrogens that have potent apoptotic activity against rapidly growing PCa cells, 68 prompting the testing of combinatory therapies involving methoxyestrogens and other standard therapies, such as hormone deprivation, 69 docetaxel, 70 and eugenol 71 against PCa growth in model systems.…”
Section: Influence Of Estrogen Bioactivation and Detoxification On Pcmentioning
confidence: 99%
“…67 Supporting the suggestion that the genotoxicity of estrogen metabolites is involved in prostate carcinogenesis is the observation of increased DNA strand breakage 52 and nuclear staining of 8-hydroxy-2′-deoxy-guanosine 60 in the prostates of rats treated with T plus E2. Conversely, increased expression or activity of COMT was shown to protect against estrogen-induced cancer by mediating the conversion of catechol estrogens into methoxyestrogens that have potent apoptotic activity against rapidly growing PCa cells, 68 prompting the testing of combinatory therapies involving methoxyestrogens and other standard therapies, such as hormone deprivation, 69 docetaxel, 70 and eugenol 71 against PCa growth in model systems.…”
Section: Influence Of Estrogen Bioactivation and Detoxification On Pcmentioning
confidence: 99%
“…Although eugenol was shown to induce apoptosis in cancer cell lines, there are no reports on the effects of eugenol on the hallmark capabilities of chemically induced tumours in animal models (Yoo et al 2005;Pisano et al 2007;Ghosh et al 2009). Recently, we demonstrated that eugenol inhibits cell proliferation via suppression of nuclear factor-kappaB (NF-κB) signaling in a rat model of gastric carcinogenesis induced by N-methyl-N′-nitro-N-nitrosoguanidine (MNNG) (Manikandan et al in press).…”
Section: Introductionmentioning
confidence: 99%
“…Previous studies showed that eugenol has a strong anticancer potential against melanoma (Pisano et al, ), osteosarcoma (Shin et al, ), acute lymphoblastic leukemia and hepatocellular carcinoma (Khalafalla et al, ), gastric cancer (Manikandan, Vinothini, Priyadarsini, Prathiba, & Nagini, ), skin tumor (Kaur, Athar, & Alam, ), mast cells (Park et al, ), and prostate cancer (Ghosh, Ganapathy, Alworth, Chan, & Kumar, ). Sharma, Paliwal, Janmeda, and Sharma () reported that the enzyme, that is, glutathione and glutathione S‐transferase (protection against carcinogens) activity loss was recovered by MO pod extract.…”
Section: Resultsmentioning
confidence: 99%