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http://dx.doi.org/10.4196/kjpp.2016.20.3.297

Klotho plays a critical role in clear cell renal cell carcinoma progression and clinical outcome  

Kim, Ji-Hee (Department of Physiology and Global Medical Science, Yonsei University Wonju College of Medicine)
Hwang, Kyu-Hee (Department of Physiology and Global Medical Science, Yonsei University Wonju College of Medicine)
Lkhagvadorj, Sayamaa (Department of Pathology, Yonsei University Wonju College of Medicine)
Jung, Jae Hung (Department of Urology, Yonsei University Wonju College of Medicine)
Chung, Hyun Chul (Department of Urology, Yonsei University Wonju College of Medicine)
Park, Kyu-Sang (Department of Physiology and Global Medical Science, Yonsei University Wonju College of Medicine)
Kong, In Deok (Department of Physiology and Global Medical Science, Yonsei University Wonju College of Medicine)
Eom, Minseob (Department of Pathology, Yonsei University Wonju College of Medicine)
Cha, Seung-Kuy (Department of Physiology and Global Medical Science, Yonsei University Wonju College of Medicine)
Publication Information
The Korean Journal of Physiology and Pharmacology / v.20, no.3, 2016 , pp. 297-304 More about this Journal
Abstract
Klotho functions as a tumor suppressor predominantly expressed in renal tubular cells, the origin of clear cell renal cell carcinoma (ccRCC). Altered expression and/or activity of growth factor receptor have been implicated in ccRCC development. Although Klotho suppresses a tumor progression through growth factor receptor signaling including insulin-like growth factor-1 receptor (IGF-1R), the role of Klotho acting on IGF-1R in ccRCC and its clinical relevance remains obscure. Here, we show that Klotho is favorable prognostic factor for ccRCC and exerts tumor suppressive role for ccRCC through inhibiting IGF-1R signaling. Our data shows the following key findings. First, in tumor tissues, the level of Klotho and IGF-1R expression are low or high, respectively, compared to that of adjacent non-neoplastic parenchyma. Second, the Klotho expression is clearly low in higher grade of ccRCC and is closely associated with clinical outcomes in tumor progression. Third, Klotho suppresses IGF-1-stimulated cell proliferation and migration by inhibiting PI3K/Akt pathway. These results provide compelling evidence supporting that Klotho acting on IGF-1R signaling functions as tumor suppressor in ccRCC and suggest that Klotho is a potential carcinostatis substance for ccRCC.
Keywords
Clear cell renal cell carcinoma; IGF-1 receptor; Klotho; Migration; Prognosis;
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