Hepatitis B Virus X ÇüÁúÀüȯ »ýÁã¿Í ÀÎü °£¼¼Æ÷¾ÏÁ¾¿¡¼ Proliferating Cell Nuclear Antigen ¹ßÇö°ú ÀÚ¸ê»ç
A Study on the Expression of Proliferating Cell Nuclear Antigen and Apoptosis of theHepatocellular Carcinoma in Human and Hepatitis B Virus X Transgenic Mice
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¹®Çü¹è ( Moon Hyung-Bae )
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À¯´ë¿ ( Yu Dae-Yeul )
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À¯Çü·û ( Yoo Hyung-Ryun )
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¼Òº´ÁØ ( So Byung-Joon )
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ä±Ç¹¬ ( Chae Kwon-Mook )
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±èÇÐö ( Kim Haak-Cheol )
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À±±âÁß ( Yun Ki-Jung )
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ÇÑ¿øö ( Han Won-Cheol )
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Á¶ÇâÁ¤ ( Jo Hyang-Jeong )
¿ø±¤´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
±èº¸¿ë ( Kim Bo-Yong )
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KMID : 0357920010350020129
Abstract
Background: This experiment was designed to study the cell kinetics of hepatocellular carcinoma (HCC) in both hepatitis B virus X (HBx) transgenic mice and humans.
Methods: The immunohistochemical stain of proliferating cell nuclear antigen (PCNA) and TdT-mediated dUTP-biotin nick end labeling (TUNEL) assay of apoptosis were used on formalin fixed-paraffin embedded tissues.
Results: PCNA labeling indices (PCNA-LI) in the liver of HBx transgenic mice were markedly increased in HCC (11.3%) compare to the dysplastic areas (1.3%) and in the liver of non-transgenic littermates (0.1%). There was no significant difference of PCNA-LI in the dysplastic areas between HCC developed mice and non-HCC developed mice. Apoptosis labeling indices (Apoptosis-LI) in both the dysplastic areas and HCC of HBx transgenic mice were similar to those of non-transgenic littermates. PCNA-LI was markedly increased in human HCC (28.9%) compare to the background of HCC (2.9%) and the control liver (2.9%). Apoptosis-LI was decreased in human HCC (0.3%) compare to the background of HCC (0.4%) and the control liver (1.0%).
Conclusion: There is a marked increase of cell proliferating activity in human HCC and in HCC of HBx transgenic mice, and there is a decrease of apoptosis in human HCC, but not in HCC of HBx transgenic mice.
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Transgenic;Hepatocellular;Carcinoma;Proliferating cell nuclear antigen;Apoptosis
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