• 1. 西藏軍區(qū)總醫(yī)院外一科(拉薩850003)2. 第三軍醫(yī)大學大坪醫(yī)院普外科;

用裸小鼠胃癌細胞移植瘤作為體內誘導分化研究模型,采用移植瘤生長狀態(tài)、移植瘤組織學、超微結構、細胞周期動力學變化及移植瘤p53、p21蛋白表達作為指標,研究了不同劑量的全反式維甲酸(ATRA)對裸小鼠胃癌細胞移植瘤的抗增殖及誘導分化作用。結果發(fā)現:在ATRA 300~1 000μg/只·d的劑量下,對移植瘤具有明顯生長抑制作用,并對移植瘤細胞有較強的誘導分化作用;同時可抑制移植瘤癌細胞p53、p21的表達。本實驗結果提示:ATRA在體內對人胃癌細胞有較強的抗增殖和誘導分化作用,這種抗癌作用可能與ATRA抑制癌細胞p53及p21表達,促進癌細胞凋亡有密切關系。

引用本文: 黃承良,王代科,劉寶華. 全反式維甲酸對人胃癌裸小鼠移植瘤的抗增殖及誘導分化作用. 中國普外基礎與臨床雜志, 1998, 5(3): 129-131. doi: 復制

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  2. 2. D.施梅爾著.惡性腫瘤的發(fā)生、生長和化療.第1版.北京:科學技術出版社,1984∶445.
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  4. 4. Brooc JSJ. Analytic false positivity with immunohistochemistry. Am J Clin Pathol, 1984; 82(1)∶134.
  5. 5. 沈敏,許建明,童菊芳等.全反式維甲酸對胃癌細胞株SGC7901的抗增殖及誘導分化作用的研究.中國藥學雜志, 1991; 26(12)∶722.
  6. 6. Skashita A, Ress J, Kadin M, et al. 9cis retinoic acid: effects on normal and leukemia hepatopoiesis in vitro. Blood, 1996; 81(5)∶1009.
  7. 7. Gwyn T, Saurit G, Moria C, et al. Molecular regulation of apoptosis: genetic controls on cell death. Cell, 1993; 74(6)∶777.
  8. 8. Kerin JK, Green MH, Berg J, et al. Evidence for the involvement of RAR dependent signaling pathway in the induction of tissue transglutaminase and apoptosis by retinoids. J Bio Chem, 1995; 11(2)∶6022.