Matsumura Y, Sugiyama M, Matsumura S, Hayle A J, Robinson P, Smith J C, Tarin D
Nuffield Department of Pathology, university of Oxford, John Radcliffe Hospital, Headington, U.K.
J Pathol. 1995 Sep;177(1):11-20. doi: 10.1002/path.1711770104.
Increased and disorganised expression of CD44 variant exons has been demonstrated in biopsy samples of several types of human malignancy by many groups. This abnormality can be used to detect exfoliated tumour cells in the urine of bladder cancer patients. The present report demonstrates that the deranged activity of this gene in neoplasia also results in the accumulation of immature mRNA transcripts containing non-coding sequences (introns) from this gene in cancer tissues and cells. There is simultaneous overexpression of a newly identified 437 bp exon (coding sequence) located in the variably active region of the gene and of many abnormal variant exon combinations. This is the first report describing the specific retention of introns in gene transcripts in clinical diagnostic samples of tumour tissues and cells. The phenomenon was seen repeatedly in samples from cancer patients and in a cancer cell line, and thus could form the basis for a unique new and specific method of cancer diagnosis.
许多研究小组已证实,在多种人类恶性肿瘤的活检样本中,CD44可变外显子的表达增加且紊乱。这种异常可用于检测膀胱癌患者尿液中的脱落肿瘤细胞。本报告表明,该基因在肿瘤形成过程中的紊乱活性还导致癌症组织和细胞中积累了含有该基因非编码序列(内含子)的未成熟mRNA转录本。位于该基因可变活性区域的一个新鉴定的437 bp外显子(编码序列)以及许多异常可变外显子组合同时过度表达。这是第一份描述肿瘤组织和细胞临床诊断样本中基因转录本内含子特异性保留的报告。这种现象在癌症患者的样本和癌细胞系中反复出现,因此可为一种独特的新型癌症诊断方法奠定基础。