Hibi K, Trink B, Patturajan M, Westra W H, Caballero O L, Hill D E, Ratovitski E A, Jen J, Sidransky D
Department of Otolaryngology-Head and Neck Surgery, Division of Head and Neck Cancer Research, Johns Hopkins University School of Medicine, 818 Ross Research Building, 720 Rutland Avenue, Baltimore, MD 21205-2196, USA.
Proc Natl Acad Sci U S A. 2000 May 9;97(10):5462-7. doi: 10.1073/pnas.97.10.5462.
We and others recently isolated a human p53 homologue (p40/p51/p63/p73L) and localized the gene to the distal long arm of chromosome 3. Here we sought to examine the role of p40/p73L, two variants lacking the N-terminal transactivation domain, in cancer. Fluorescent in situ hybridization (FISH) analysis revealed frequent amplification of this gene locus in primary squamous cell carcinoma of the lung and head and neck cancer cell lines. (We named this locus AIS for amplified in squamous cell carcinoma.) Furthermore, amplification of the AIS locus was accompanied by RNA and protein overexpression of a variant p68(AIS) lacking the terminal transactivation domain. Protein overexpression in primary lung tumors was limited to squamous cell carcinoma and tumors known to harbor a high frequency of p53 mutations. Overexpression of p40(AIS) in Rat 1a cells led to an increase in soft agar growth and tumor size in mice. Our results support the idea that AIS plays an oncogenic role in human cancer.
我们和其他研究人员最近分离出一种人类p53同源物(p40/p51/p63/p73L),并将该基因定位到3号染色体长臂远端。在此,我们试图研究p40/p73L这两种缺乏N端反式激活结构域的变体在癌症中的作用。荧光原位杂交(FISH)分析显示,该基因座在原发性肺鳞状细胞癌和头颈部癌细胞系中频繁扩增。(我们将这个基因座命名为AIS,即鳞状细胞癌中扩增的基因座。)此外,AIS基因座的扩增伴随着一种缺乏末端反式激活结构域的变体p68(AIS)的RNA和蛋白质过度表达。原发性肺肿瘤中的蛋白质过度表达仅限于鳞状细胞癌以及已知携带高频p53突变的肿瘤。在大鼠1a细胞中p40(AIS)的过度表达导致小鼠软琼脂生长增加和肿瘤大小增大。我们的结果支持AIS在人类癌症中起致癌作用这一观点。