Bricker L A, Morris H P, Siperstein M D
J Clin Invest. 1972 Feb;51(2):206-15. doi: 10.1172/JCI106805.
By means of the desmosterol suppression technique described in the previous paper, the influence of hepatomas on sterol metabolism has been studied in the intact rat. The major finding of this study is that all hepatoma-bearing rats demonstrate a consistent in vivo loss of the cholesterol feedback system that is characteristic of normal liver. The results also demonstrate that such tumors retain only minor amounts of the sterol they synthesize, releasing over 90% of such endogenous sterol into the circulation. Finally, the in vivo loss of cholesterol feedback control was found to occur in at least two minimal deviation hepatomas and in one highly malignant adenocarcinoma of hepatic origin. These findings indicate that even tumors that are capable of only very limited cholesterol synthesis in vitro, can contribute significant quantities of sterol to the bloodstream. It is concluded that as a result of their lack of normal cholesterol feedback control, hepatomas may represent a physiologically important source of sterols in the tumor-bearing animal, and that the absence of feedback control of sterol synthesis may provide a means of detecting the presence of such tumors in the intact animal.
运用上一篇论文中描述的去氢胆甾醇抑制技术,在完整大鼠体内研究了肝癌对甾醇代谢的影响。本研究的主要发现是,所有荷肝癌大鼠体内均表现出正常肝脏所特有的胆固醇反馈系统持续缺失。结果还表明,此类肿瘤仅保留其合成甾醇的少量部分,将超过90%的内源性甾醇释放到循环中。最后,发现至少在两种微小偏离型肝癌和一种肝源性高恶性腺癌中发生了胆固醇反馈控制的体内缺失。这些发现表明,即使是在体外仅能进行非常有限胆固醇合成的肿瘤,也能向血液中贡献大量甾醇。得出的结论是,由于缺乏正常的胆固醇反馈控制,肝癌可能是荷瘤动物体内甾醇的一个重要生理来源,并且甾醇合成反馈控制的缺失可能为在完整动物体内检测此类肿瘤的存在提供一种方法。