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Если это нарушение проникает в дочерние клетки первого этапа, то оно будет передаваться всем последующим поколениям клеток с перспективой превратиться в клинически выявляемое раковое заболевание. Однако это упрощение очень сложного процесса. Две существенные гипотезы, похоже, оставлены без внимания: 1) для появления и развития рака нужно больше чем одна мутация и 2) не все генетические нарушения приводят к возникновению онкологических заболеваний.
