Àá½Ã¸¸ ±â´Ù·Á ÁÖ¼¼¿ä. ·ÎµùÁßÀÔ´Ï´Ù.

DiethylnitrosamineÀ¸·Î À¯µµµÈ ÈòÁãÀÇ °£¼¼Æ÷¾ÏÁ¾ ¹ß»ý °úÁ¤¿¡¼­ Transforming Growth Factor (TGF)-¥â1°ú TGF-¥â Receptor II¿¡ ´ëÇÑ ¸é¿ªÁ¶Á÷È­Çп°»ö ¹× TGF-¥â1 mRNAÀÇ Á¤·®Àû ºÐ¼® Immunohistochemical Analysis of Transforming Growth Factor (TGF)-¥â1 and TGF-¥â Receptor II and Quantitative Analysis of TGF-¥â1 mRNA during Multistep Hepatocarcinogenesis Induced by Diethylnitrosamine in Sprague-Dawley Rats

´ëÇѺ´¸®ÇÐȸÁö 1999³â 33±Ç 11È£ p.1009 ~ 1023
Á¶¹Ì¿¬, ÀÌÁÖÇÑ, °­¿ë±¸, ¿ø³²Èñ,
¼Ò¼Ó »ó¼¼Á¤º¸
Á¶¹Ì¿¬ ( Cho Mee-Yon ) 
¿¬¼¼´ëÇб³ ¿øÁÖÀÇ°ú´ëÇÐ º´¸®Çб³½Ç

ÀÌÁÖÇÑ ( Lee Ju-Han ) 
°í·Á´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
°­¿ë±¸ ( Kang Yong-Koo ) 
°í·Á´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
¿ø³²Èñ ( Won Nam-Hee ) 
°í·Á´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç

Abstract


Transforming growth factor (TGF)-¥â1 plays an important role in hepatocarcinogenesis and has been described as a useful tumor marker and one of the poor prognostic indicators in patients with hepatocellular carcinoma (HCC). To investigate the role and cellular localization of TGF-¥â1 during multistep hepatocarcinogenesis we performed a quantitative analysis of TGF-¥â1 mRNA and immunohistochemical expression of TGF-¥â1 and TGF-¥â receptor II (TGF-¥ârII) in female Sprague-Dawley rats. The experimental groups included neoplastic lesions produced by Solt-Farber¡¯s protocol, regenerating liver after partial hepatectomy, and normal control. Quantitative change of TGF-¥â1 mRNA was analysed by competitive reverse-transcription polymerase chain reaction (RT-PCR). TGF-¥â1 protein and TGF-¥ârII expression were evaluated by immunohistochemical stain. The discrete tumor nodules were detected on 14th day and then increased in number and size. Three HCCs were induced on 8th or 9th month. RT-PCR demonstrated TGF-¥â1 mRNA band in all examples of the normal and regenerating liver, nodules and HCCs. Competitive RT-PCR displayed higher TGF-¥â1 mRNA in nodules, HCCs and regenerating liver than in normal controls. Hepatocytes from control and regenerating livers showed weak immunoreactivity for TGF-¥â1. In contrast, the cytoplasm of hepatocytes of nodules in 7th, 8th and 9th month and HCCs were intensely stained for TGF-¥â1. Some sinusoidal cells showed immunoreactivity for TGF-¥â1 in all experimental groups. In early phase of carcinogenesis, the cytoplasm of hepatocytes in liver of 12h, 1d and 3d showed transiently increased immunoreactivity for TGF-¥â1 and The immunoreactivity decreased thereafter. TGF-¥â1 mRNA was also detected in the neoplastic hepatocytes by in-situ hybridization. Although TGF-¥ârII expression was correlated with TGF-¥â1 immunoreactivity during early phase of carcinogenesis, hepatocytes in most nodules in 7th, 8th, 9th month and carcinomas showed decreased or little immunoreactivity for TGF-¥ârII. Based on the above results, it is concluded that TGF-¥â1 expression increases not only in precancerous nodules but also in HCCs and its increase seems to be correlated with decrease or loss of TGF-¥ârII expression although its mechanism remains unclear. Hepatocytes may be a major cellular source of TGF-¥â1 during hepatocarcinogenesis.

Å°¿öµå

TGF-¥â1;TGF-¥â receptor II;Hepatocarcinogenesis;Competitive RT-PCR

¿ø¹® ¹× ¸µÅ©¾Æ¿ô Á¤º¸

  

µîÀçÀú³Î Á¤º¸

KCI
KoreaMed
KAMS