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Novel genetic and epigenetic alterations in ... - Ous-research.no

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PREFACE“Is it just me? Or does everyonecome across <strong>genetic</strong>s, genes, <strong>and</strong>DNA almost everywhere?”Madele<strong>in</strong>e AlbrightCancer as a disease has probably been around s<strong>in</strong>ce the dawn of multicellular organisms. Theoldest written description of cancer is as early as the 17 th century BC <strong>in</strong> Egypt[1], but tracesof cancer has been detected as far back as <strong>in</strong> d<strong>in</strong>osaur fossils. Accord<strong>in</strong>g to the humoraltheory, it was believed that it was excess of black bile that was responsible for cancer as awhole. If this theory is correct the production of this body fluid must either have <strong>in</strong>creasedrapidly over the last centuries, or <strong>in</strong>crease with age, as one out of three people are diag<strong>no</strong>sedwith cancer today. Now we k<strong>no</strong>w that the black bile-theory did <strong>no</strong>t st<strong>and</strong> the tooth of time,<strong>and</strong> that cancer is caused by both genes <strong>and</strong> environmental factors which via <strong>genetic</strong> <strong>and</strong>epi<strong>genetic</strong> ab<strong>no</strong>rmalities make <strong>no</strong>rmal regulation of e.g. cell cycle, apoptosis <strong>and</strong> signal<strong>in</strong>g goawry.With improved life expectancy <strong>and</strong> a more sedentary lifestyle comes <strong>in</strong>creased lifetime risk ofbe<strong>in</strong>g diag<strong>no</strong>sed with cancer. Only <strong>in</strong> very rare occasions the primary tumor itself is fatal, butwhen the tumor metastasizes to distant <strong>and</strong> vital organs the mortality <strong>in</strong>creases rapidly. As ittakes time from the first <strong>alterations</strong> via precursor lesions <strong>and</strong> the primary - to a fullymetastasized cancer, it leaves a w<strong>in</strong>dow of opportunity <strong>in</strong> which the evolv<strong>in</strong>g cancer can bedetected <strong>and</strong> the person cured if the suitable tool or biomarkers is at h<strong>and</strong>.In September 2007, 4 years after the completion of the human ge<strong>no</strong>me project, the first<strong>in</strong>dividual ge<strong>no</strong>me was published[2]. Just a few moths later, the ge<strong>no</strong>me of James D. Watson,the co-discoverer of the double helix, was published us<strong>in</strong>g modern ultra high-throughput6

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