Department of Biomedical Sciences, Graduate School of Health Sciences, Hirosaki University, Hirosaki, Japan.
Department of Medical Welfare, Akita University of Nursing and Welfare, Odate, Japan.
Cancer Med. 2024 Sep;13(18):e70165. doi: 10.1002/cam4.70165.
Cancer initiation has long been "unknowable" in biology and medicine. In 1987, however, Moore and our research group observed single hepatocytes and minifoci that were strongly positive for glutathione S-transferase P-form (GST-P) in the rat liver as early as 2 to 3 days after initiation by diethylnitrosamine prior to the induction of GST-P foci and nodules. The induction of GST-P single hepatocytes, precursors of GST-P foci and nodules, was considered genetic. But, the details of the induction mechanism have remained unclear despite various examinations over a long period.
Male Sprague-Dawley rats (aged 6 weeks) were fed a basal diet containing either benzyl isothiocyanate (BITC, 0.5% by wt) or 2-acetylaminofluorene (AAF, 0.04%) ad libitum for appropriate time intervals. All animals were anesthetized and euthanized. The livers obtained were excised, cut into 3- to 4-mm-thick slices and fixed in cold acetone at 4 °C. The liver specimens were then sliced into 25-µm-thick sections in PBS using an automated microtome (Vibratome 1500 Sectioning System, Vibratome Products, NY, USA). Immunocytochemical staining was performed in free solution, and the results were examined via digital light microscopy (Coolscope, Nikon, Tokyo).
3D analysis using a vibratome showed that GST-P is rapidly excreted into the bile of the liver of animals in response to strong carcinogenic stress caused by promoters or initiators. "Rapid biliary excretion of GST-P" was widely and commonly observed in all hepatocytes, GST-P single hepatocytes, minifoci, foci and nodules under appropriate conditions. Surprisingly, on the basis of these key findings, a new mechanism of cancer initiation involving the transformation of hepatocytes into GST-P single hepatocytes and minifoci in animal livers was identified. In addition, the initiation process was determined to be nongenetic because mutation is an invisible rare event.
This short review describes several details about breakthrough findings on cancer initiation in rat livers, the application of 3D analysis to other cancers and the importance in the genetic analysis in malignant diseases.
癌症的发生在生物学和医学上长期以来一直是“不可知”的。然而,早在 1987 年,摩尔和我们的研究小组就观察到,在用二乙基亚硝胺引发 GST-P 灶和结节之前,早在 2 至 3 天,大鼠肝脏中就已经存在强烈表达谷胱甘肽 S-转移酶 P 形式(GST-P)的单个肝细胞和微灶。GST-P 单肝细胞的诱导被认为是遗传的,这些细胞是 GST-P 灶和结节的前体。但是,尽管经过了很长一段时间的各种检查,诱导机制的细节仍然不清楚。
雄性 Sprague-Dawley 大鼠(6 周龄)自由喂食含有苄基异硫氰酸酯(BITC,0.5%重量比)或 2-乙酰氨基芴(AAF,0.04%)的基础饮食。所有动物均麻醉并安乐死。取出肝脏,切成 3 至 4 毫米厚的切片,在 4°C 的冷丙酮中固定。然后使用自动切片机(Vibratome 1500 切片系统,Vibratome Products,NY,USA)将肝标本在 PBS 中切成 25 µm 厚的切片。在游离溶液中进行免疫细胞化学染色,并通过数字光显微镜(尼康 Coolscope,东京)进行检查。
使用切片机进行的 3D 分析表明,GST-P 迅速分泌到肝脏的胆汁中,以响应启动子或引发剂引起的强烈致癌应激。在适当的条件下,“GST-P 的快速胆汁排泄”广泛而普遍地观察到所有肝细胞、GST-P 单肝细胞、微灶、灶和结节中。令人惊讶的是,基于这些关键发现,确定了一种新的癌症发生机制,涉及肝细胞转化为动物肝脏中的 GST-P 单肝细胞和微灶。此外,由于突变是一种不可见的罕见事件,因此该启动过程是非遗传的。
这篇简短的综述描述了大鼠肝脏中癌症发生的一些突破性发现、3D 分析在其他癌症中的应用以及恶性疾病中遗传分析的重要性。