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J Mol Histol ; 44(1): 111-6, 2013 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-23093412

RESUMO

Oxidative stress is associated with many disease states including gynecologic disease. This process can damage lipids, proteins and DNA. The present study highlights the role of oxidative stress induced DNA damage as measured by 8-hydroxy-2-deoxyguanosine in development of benign gynecological conditions (BGC). Our aim was to map the oxidative DNA damage on female reproductive organs and highlight the high amount found in a variety of benign gynecologic disorders. Seventeen biopsy specimens from female pelvic organs were divided in two groups: healthy organs tissue and BGC tissue. Healthy organs biopsy tissue included the cervix, tubes, uterus, peritoneum, and topic endometrium in secretory phase. Benign gynecological biopsy tissue included hydrosalpinges, leiomyoma, adenomyosis and tubal cysts. Immunohistochemical staining showed significantly higher levels of DNA damage between BGC and healthy organs [19.36 % (6.20; 32.51) vs. 4.61 % (0.63; 8.53); P < 0.0344]. Our results highlight the involvement of oxidative stress DNA damage in female benign pelvic disease. Hydrosalpinges, leiomyoma, and adenomyosis exhibit the highest amounts of oxidative DNA damage in the pelvic cavity.


Assuntos
Desoxiguanosina/análogos & derivados , Genitália Feminina/metabolismo , 8-Hidroxi-2'-Desoxiguanosina , Adenomiose/metabolismo , Adenomiose/patologia , Adulto , Colo do Útero/citologia , Colo do Útero/metabolismo , Desoxiguanosina/metabolismo , Feminino , Humanos , Pessoa de Meia-Idade
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