Gemma Akihiko
4th Department of Internal Medicine, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, Tokyo 113-8602, Japan.
Gan To Kagaku Ryoho. 2002 Dec;29(13):2451-7.
The genomic alterations in preneoplastic lesions are summarized in this review. 3p and 9p in the lung, 9p in the bladder, 8p in the prostata, 19q and 1p in oligodendroglioma, and 22q in meningioma were reported to be deleted. Somatic mutation of p53 was found in preneoplastic lesions of the esophagus, stomach, colon, thyroid, and astrocytoma. Adenoma-carcinoma sequence (Apc, ras, p53 gene alterations) in colon, LKB1 gene in Peutz-Jeghers syndrome, Smad4 in juvenile polyposis, hMSH2, hMLH1, PMS1, PMS2 genes in HNPCC, VHL gene in kidney, WT1 in Wilms tumor, RB gene in retinoblastoma, and ret gene in MEN were reportedly altered in preneoplastic lesions involved in hereditary tumors. Cervical dysplasia and papilloma of the head and neck infected by human papilloma virus and liver infected by B-type hepatitis virus are also precancerous. Genomic instability, APC gene alteration, point mutation of K-ras in preneoplastic lesions of stomach and K-ras and p16 alterations in metaplasia of pancreas were also found. Advances in research on genomic alterations in preneoplastic lesions will contribute to prevention and early detection of cancer.
本综述总结了癌前病变中的基因组改变。据报道,肺中的3p和9p、膀胱中的9p、前列腺中的8p、少突胶质细胞瘤中的19q和1p以及脑膜瘤中的22q存在缺失。在食管、胃、结肠、甲状腺和星形细胞瘤的癌前病变中发现了p53的体细胞突变。在结肠癌的腺瘤-癌序列(Apc、ras、p53基因改变)、黑斑息肉综合征中的LKB1基因、幼年性息肉病中的Smad4、遗传性非息肉病性结直肠癌中的hMSH2、hMLH1、PMS1、PMS2基因、肾中的VHL基因、肾母细胞瘤中的WT1、视网膜母细胞瘤中的RB基因以及多发性内分泌腺瘤病中的ret基因在遗传性肿瘤相关的癌前病变中均有改变。人乳头瘤病毒感染的宫颈发育异常和头颈部乳头状瘤以及B型肝炎病毒感染的肝脏也属于癌前病变。还发现了胃癌前病变中的基因组不稳定性、APC基因改变、K-ras点突变以及胰腺化生中的K-ras和p16改变。癌前病变基因组改变的研究进展将有助于癌症的预防和早期检测。