High serum HTATIP2/TIP30 level in serous ovarian cancer as prognostic or diagnostic marker
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  • 作者:Yakup Kumtepe (1)
    Zekai Halici (2)
    Ozlem Sengul (3)
    Celalettin Semih Kunak (4)
    Yasin Bayir (5)
    Nergiz Kilic (6)
    Elif Cadirci (7)
    Alparslan Pulur (1)
    Zafer Bayraktutan (8)
  • 关键词:HTATIP2/TIP30 ; ovarian cancer ; adenocarcinoma
  • 刊名:European Journal of Medical Research
  • 出版年:2013
  • 出版时间:December 2013
  • 年:2013
  • 卷:18
  • 期:1
  • 全文大小:174KB
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  • 作者单位:Yakup Kumtepe (1)
    Zekai Halici (2)
    Ozlem Sengul (3)
    Celalettin Semih Kunak (4)
    Yasin Bayir (5)
    Nergiz Kilic (6)
    Elif Cadirci (7)
    Alparslan Pulur (1)
    Zafer Bayraktutan (8)

    1. Department of Obstetrics and Gynecology, Faculty of Medicine, Ataturk University, Erzurum, 25240, Turkey
    2. Department of Pharmacology, Faculty of Medicine, Ataturk University, Erzurum, 25240, Turkey
    3. Department of Gynecology and Obstetrics, Yenimahalle Government Hospital, Ankara, 06170, Yenimahalle, Turkey
    4. Department of Pharmacology, Faculty of Medicine, Giresun University, Giresun, 28100, Turkey
    5. Department of Biochemistry, Faculty of Pharmacy, Ataturk University, Erzurum, 25240, Turkey
    6. Department of Obstetrics and Gynecology, Faculty of Medicine, Kafkas University, Kars, 36000, Turkey
    7. Department of Pharmacology, Faculty of Pharmacy, Ataturk University, Erzurum, 25240, Turkey
    8. Department of Biochemistry, Erzurum Region Education and Research Hospital, Erzurum, 25240, Turkey
  • ISSN:2047-783X
文摘
Background Human HIV-1 TAT interactive protein 2 (HTATIP2/TIP30) is an evolutionarily conserved gene that is expressed ubiquitously in human tissues and some tumor tissues. This protein has been found to be associated with some gynecological cancers; as such, this study aimed to investigate blood HTATIP2/TIP30 levels in patients with ovarian cancer. Methods Twenty-three women with ovarian cancer and 18 patients with various non-cancerous gynecological complaints (for example, dysfunctional uterine bleeding, fibroids, and urinary incontinence) were included in the study. The pathological diagnosis of ovarian cancer was adenocarcinoma. HTATIP2/TIP30 concentration in the patients-blood samples was determined using ELISA kits. Results The HTATIP2/TIP30 level was significantly higher in the cancer group than in the control group (1.84 ± 0.82 versus 0.57 ± 0.13 ng/ml, mean ± SD). Conclusions We demonstrated the potential role of HTATIP2/TIP30 in ovarian cancer for the first time, thereby enlightening future studies targeting HTATIP2/TIP30 in ovarian cancer treatment, diagnosis, and prevention.

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