Down-regulation of 8-hydroxydeoxyguanosine and peroxiredoxin II in the pathogenesis of endometriosis-associated ovarian cancer

Henri Sova, Sova H, Juha Kangas, Kangas J, Puistola U, Ulla Puistola, Markku Santala, Santala M, Annikki Liakka, Liakka A, Karihtala P, Peeter Karihtala
Anticancer research · 2012 · vol. 32(8) , pp. 3037–44 · PMID:22843871 · W2157858295
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Endometriosis-associated ovarian cancer showed significantly weaker nuclear 8-hydroxydeoxyguanosine and peroxiredoxin II expression compared to benign endometriosis and adjacent endometriosis tissue.

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Abstract

AIM: To evaluate the roles of oxidative stress marker 8-hydroxydeoxyguanosine (8-OHdG) and peroxiredoxin (PRX) antioxidants in the development of endometriosis and endometriosis-associated ovarian cancer (EAC). MATERIALS AND METHODS: Tissue expressions of 8-OHdG, PRX II and PRX IV were determined immunohistochemically in tissue from 22 women with benign endometriosis (BE) and 33 women with EAC, among whom endometriosis and cancer tissues were analyzed separately. RESULTS: When all three groups were compared simultaneously, EAC tumor cells had significantly weaker nuclear 8-OHdG and PRX II expression (p<0.05 and p<0.01, respectively) and significantly weaker cytoplasmic 8-OHdG expression (p<0.01) than EAC endometriosis and BE epithelial cells. This same trend was also observed when groups were compared pair-wise. CONCLUSION: Nuclear PRX II and 8-OHdG were down-regulated in EAC tumorous tissue compared with BE and EAC endometriotic tissue, suggesting a role of oxidative stress in the pathogenesis of EAC.

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Condition tags

endometriosis

MeSH descriptors

Deoxyguanosine Down-Regulation Down-Regulation Endometriosis Ovarian Neoplasms Peroxiredoxins 8-Hydroxy-2'-Deoxyguanosine 8-Hydroxy-2'-Deoxyguanosine Deoxyguanosine Deoxyguanosine Deoxyguanosine Endometriosis Endometriosis Endometriosis Female Female Humans Humans Immunohistochemistry Immunohistochemistry

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Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. Outer rings show 2-hop neighbours — papers reached through the immediate citers/citees. [ collapse to 1-hop ]

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