Hill D Ashley, Ivanovich Jennifer, Priest John R, Gurnett Christina A, Dehner Louis P, Desruisseau David, Jarzembowski Jason A, Wikenheiser-Brokamp Kathryn A, Suarez Brian K, Whelan Alison J, Williams Gretchen, Bracamontes Dawn, Messinger Yoav, Goodfellow Paul J
Washington University Medical Center, St. Louis, MO 63110, USA.
Science. 2009 Aug 21;325(5943):965. doi: 10.1126/science.1174334. Epub 2009 Jun 25.
Pleuropulmonary blastoma (PPB) is a rare pediatric lung tumor that is often part of an inherited cancer syndrome. PPBs consist of mesenchymal cells that are susceptible to malignant transformation and cysts lined by epithelial cells. In a subset of patients, overgrowth of the cysts by mesenchymal cells leads to sarcoma formation. Here, we show that 11 multiplex PPB families harbor heterozygous germline mutations in DICER1, a gene encoding an endoribonuclease critical to the generation of small noncoding regulatory RNAs. Expression of DICER1 protein was undetectable in the epithelial component of PPB tumors but was retained in the malignant mesenchyme (sarcoma). We hypothesize that loss of DICER1 in the epithelium of the developing lung alters the regulation of diffusible factors that promote mesenchymal proliferation.
胸膜肺母细胞瘤(PPB)是一种罕见的儿童肺部肿瘤,常为遗传性癌症综合征的一部分。PPB由易发生恶性转化的间充质细胞和衬有上皮细胞的囊肿组成。在一部分患者中,间充质细胞导致囊肿过度生长,进而形成肉瘤。在此,我们发现11个PPB复合家系的种系中存在DICER1基因的杂合突变,该基因编码一种对小非编码调节RNA的生成至关重要的核糖核酸内切酶。在PPB肿瘤的上皮成分中检测不到DICER1蛋白的表达,但在恶性间充质(肉瘤)中仍有保留。我们推测,发育中的肺上皮中DICER1的缺失改变了促进间充质增殖的可扩散因子的调控。