The development of cancer in humans involves a complex successionof events that usually occur over many decades. During thismultistep process, the genomes of incipient cancer cells acquiremutant alleles of proto-oncogenes, tumor-suppressor genes, andother genes that control, directly or indirectly, cell proliferation.Different combinations of these mutant alleles are found inthe genomes of the many distinct types of human cancer as wellas in different cancers from the same tissue. An ever-increasingnumber of these genes have been shown to make contributionsto the distinct steps involved in neoplastic transformation.The complexity of these observations provokes . . . [Full Text of this Article]
Multiple Alterations in the Genomes of Cells
Simple Transforming Systems
Collaborating Oncogenes in Rodent Cells
Further Complexity in the Transformation of Human Cells
Gene Silencing by Methylation of DNA
The Genetic History of Human Cancer
The Complexity of Tumor Pathogenesis
Colorectal Cancer
A Limited Number of Acquired Phenotypes in All Cancers
Genetic Instability
Disrupted Regulatory Circuits
The Retinoblastoma Protein
The p53 Protein
Telomeres
Mitogenic Stimulation
Angiogenesis
Experimental Evidence of Key Regulatory Pathways
Introduction of Genes into Cultured Cells
Immortalization, Crisis, and Transformation
Emerging Rules Governing Human Cancer Development
Source Information
From the Department of Medical Oncology, DanaFarber Cancer Institute, and the Department of Medicine, Brigham and Women's Hospital, Boston (W.C.H.); and the Whitehead Institute for Biomedical Research and the Department of Biology, Massachusetts Institute of Technology, Cambridge (R.A.W.).
Address reprint requests to Dr. Hahn at the Department of Medical Oncology, DanaFarber Cancer Institute, 44 Binney St., Boston, MA 02115, or at william_hahn@dfci.harvard.edu.
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