Sulong Sarina, Yusoff Abdul Aziz Mohamed, Zainuddin Norafiza, Abdullah Jafri Malin, Pannatil Jain George, Jaafar Hasnan, Isa Mohd Nizam
Human Genome Center, Department of Neurosciences.
Malays J Med Sci. 2004 Jan;11(1):37-43.
The new millennium has been regarded as a genomic era. A lot of researchers and pathologists are beginning to understand the scientific basis of molecular genetics and relates with the progression of the diseases. Central nervous system (CNS) tumours are among the most rapidly fatal of all cancers. It has been proposed that the progression of malignant tumours may result from multi-step of genetic alterations, including activation of oncogenes, inactivation of tumour suppressor genes and also the presence of certain molecular marker such as telomerase activity. In this paper, we review some recent data from the literature, including our own studies, on the molecular genetics analysis in CNS tumours. Our studies have shown that two types of tumour suppressor genes, p53 and PTEN were involved in the development of these tumours but not in p16 gene among the patients from Hospital Universiti Sains Malaysia (HUSM). Telomerase activity also has been detected in various types of CNS tumours. Thus, it is important to assemble all data which related to this study and may provide as a vital information in a new approach to neuro-oncology studies in Malaysia.
新千年被视为基因组时代。许多研究人员和病理学家开始理解分子遗传学的科学基础及其与疾病进展的关系。中枢神经系统(CNS)肿瘤是所有癌症中致死速度最快的肿瘤之一。有人提出,恶性肿瘤的进展可能源于多步骤的基因改变,包括癌基因的激活、肿瘤抑制基因的失活以及某些分子标志物(如端粒酶活性)的存在。在本文中,我们回顾了包括我们自己的研究在内的文献中关于中枢神经系统肿瘤分子遗传学分析的一些最新数据。我们的研究表明,马来西亚理科大学医院(HUSM)的患者中,两种肿瘤抑制基因p53和PTEN参与了这些肿瘤的发生发展,但p16基因未参与。在各种类型的中枢神经系统肿瘤中也检测到了端粒酶活性。因此,汇总与本研究相关的所有数据很重要,这些数据可能为马来西亚神经肿瘤学研究的新方法提供至关重要的信息。