Salmon R J, Remvikos Y, Muleris M, Thomas G
Institut Curie, Paris.
J Chir (Paris). 1992 Jan;129(1):3-8.
There are many genetic abnormalities in colorectal cancers, and they can schematically be studied according to 3 approaches. 1. The quantitative abnormalities of the DNA content of the nucleus and the cell cycle are studied with flow cytometry. 2. Karyotypic abnormalities relating to the loss and/or gain of chromosomes or structural abnormalities are studied by cytogenetics. 3. Oncogene or anti-oncogene mutations carried out by these chromosomal segments are studied by molecular biology. When compared to the clinical data, some of these abnormalities have a prognostic value. They allow an insight into the fundamental mechanisms of colorectal carcinogenesis. Finally, they may allow predicting and assessing the efficacy of some adjunctive therapies, especially that of medication.
结直肠癌存在许多基因异常,这些异常可根据三种方法进行系统研究。1. 运用流式细胞术研究细胞核DNA含量及细胞周期的定量异常。2. 通过细胞遗传学研究与染色体丢失和/或增加相关的核型异常或结构异常。3. 利用分子生物学研究这些染色体片段发生的癌基因或抑癌基因突变。与临床数据相比,其中一些异常具有预后价值。它们有助于深入了解结直肠癌发生的基本机制。最后,它们可能有助于预测和评估某些辅助治疗的疗效,尤其是药物治疗的疗效。