1 Ocak 2019 Dergi makalesi Açık Erişim

Koyuncu, Ismail; Tuluce, Yasin; Qadir, Hewa Slahaddin; Durgun, Mustafa; Supuran, Claudiu T.

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        "affiliation": "Harran Univ, Dept Biochem, Fac Med, TR-63290 Sanliurfa, Turkey", 
        "name": "Koyuncu, Ismail"
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      {
        "affiliation": "Van Yuzuncu Yil Univ, Dept Med Biol, Fac Med, Van, Turkey", 
        "name": "Tuluce, Yasin"
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      {
        "affiliation": "Van Yuzuncu Yil Univ, Dept Med Biol, Fac Med, Van, Turkey", 
        "name": "Qadir, Hewa Slahaddin"
      }, 
      {
        "affiliation": "Harran Univ, Fac Arts & Sci, Dept Chem, Sanliurfa, Turkey", 
        "name": "Durgun, Mustafa"
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      {
        "affiliation": "Univ Firenze, Sect Pharmaceut & Nutriceut Sci, Neurofarba Dept, Via U Schiff 6, I-50019 Florence, Italy", 
        "name": "Supuran, Claudiu T."
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    "description": "Cervical cancer is a common type of cancer. Carbonic anhydrase IX (CA IX) is an attractive target for tumour therapy, being overexpressed in many cancers. We investigated the anticancer properties of the aromatic sulphonamide S-1 as a CA IX inhibitor on cervical cancer cells (HeLa) positive for CA IX expression and normal prostate epithelial cell line (PNT1-A) negative for CA IX. We examined the cytotoxic, apoptosis, genotoxic, and oxidative stress activity of S-1 on HeLa and PNT1-A cell lines. S-1 induced significant reduction of cell viability, caused apoptosis, and up-regulated ROS production. This decrease in cell survival rate can be attributed to the high level of ROS and apoptosis, which has also been shown to arrest the cell cycle. Our findings indicated that S-1 is more effective on HeLa than PNT1-A. S-1 was able to induce apoptosis of cervical cancer cells and is a possible candidate for future anticancer studies.", 
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      "issue": "1", 
      "pages": "703-711", 
      "title": "JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY", 
      "volume": "34"
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    "title": "Evaluation of the anticancer potential of a sulphonamide carbonic anhydrase IX inhibitor on cervical cancer cells"
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