Mapping histological levels of 8-hydroxy-2′-deoxyguanosine in female reproductive organs

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This study mapped oxidative DNA damage via 8-hydroxy-2′-deoxyguanosine in benign gynecological conditions, finding significantly higher levels in diseased versus healthy female reproductive organs.

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The study mapped oxidative DNA damage in female reproductive organs by measuring 8-hydroxy-2′-deoxyguanosine using immunohistochemical staining in 17 biopsy specimens, comparing healthy tissue (cervix, tubes, uterus, peritoneum, and secretory-phase endometrium) with benign gynecological conditions (hydrosalpinges, leiomyoma, adenomyosis, and tubal cysts). Benign gynecological conditions showed significantly higher levels of oxidative DNA damage than healthy organs (19.36% vs 4.61%; P < 0.0344). The authors report that hydrosalpinges, leiomyoma, and adenomyosis exhibited the highest amounts of DNA damage among the benign disorders examined. This paper is centrally about endometriosis and/or adenomyosis—specifically it includes adenomyosis biopsy samples and finds the highest oxidative DNA damage levels in adenomyosis among benign gynecologic disorders.

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Abstract

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.
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Abstract

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.

References

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MeSH descriptors

Deoxyguanosine Genitalia, Female 8-Hydroxy-2'-Deoxyguanosine Adenomyosis Adenomyosis Adenomyosis Adult Cervix Uteri Cervix Uteri Cervix Uteri Deoxyguanosine Deoxyguanosine Female Genitalia, Female Humans Middle Aged

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