Chittenden Thomas W, Howe Eleanor A, Culhane Aedin C, Sultana Razvan, Taylor Jennifer M, Holmes Chris, Quackenbush John
Department of Biostatistics and Computational Biology and Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA 02115-6084, USA.
Genomics. 2008 Jun;91(6):508-11. doi: 10.1016/j.ygeno.2008.03.002. Epub 2008 Apr 22.
A recent study published by Sjoblom and colleagues [T. Sjoblom, S. Jones, L.D. Wood, D.W. Parsons, J. Lin, T.D. Barber, D. Mandelker, R.J. Leary, J. Ptak, N. Silliman, S. Szabo, P. Buckhaults, C. Farrell, P. Meeh, S.D. Markowitz, J. Willis, D. Dawson, J.K. Willson, A.F. Gazdar, J. Hartigan, L. Wu, C. Liu, G. Parmigiani, B.H. Park, K.E. Bachman, N. Papadopoulos, B. Vogelstein, K.W. Kinzler, V.E. Velculescu, The consensus coding sequences of human breast and colorectal cancers. Science 314 (2006) 268-274.] performed comprehensive sequencing of 13,023 human genes and identified mutations in genes specific to breast and colorectal tumors, providing insight into organ-specific tumor biology. Here we present a systematic analysis of the functional classifications of Sjoblom's "CAN" genes, a subset of these validated mutant genes, that identifies novel organ-specific biological themes and molecular pathways associated with disease-specific etiology. This analysis links four somatically mutated genes associated with diverse oncological types to colorectal and breast cancers through established TGF-beta1-regulated interactions, revealing mechanistic differences in these cancers and providing potential diagnostic and therapeutic targets.
最近,Sjoblom及其同事发表的一项研究[T. Sjoblom, S. Jones, L.D. Wood, D.W. Parsons, J. Lin, T.D. Barber, D. Mandelker, R.J. Leary, J. Ptak, N. Silliman, S. Szabo, P. Buckhaults, C. Farrell, P. Meeh, S.D. Markowitz, J. Willis, D. Dawson, J.K. Willson, A.F. Gazdar, J. Hartigan, L. Wu, C. Liu, G. Parmigiani, B.H. Park, K.E. Bachman, N. Papadopoulos, B. Vogelstein, K.W. Kinzler, V.E. Velculescu, 人类乳腺癌和结直肠癌的共有编码序列。《科学》314 (2006) 268 - 274。]对13023个人类基因进行了全面测序,并鉴定出乳腺癌和结直肠癌特有的基因突变,为器官特异性肿瘤生物学提供了深入见解。在此,我们对Sjoblom的“CAN”基因(这些已验证的突变基因的一个子集)的功能分类进行了系统分析,确定了与疾病特异性病因相关的新的器官特异性生物学主题和分子途径。该分析通过已确立的TGF - β1调节的相互作用,将与多种肿瘤类型相关的四个体细胞突变基因与结直肠癌和乳腺癌联系起来,揭示了这些癌症的机制差异,并提供了潜在的诊断和治疗靶点。