DIAGNOSIS OF POLYMORPHISMS IN CARCINOGEN-ACTIVATING AND INACTIVATING ENZYMES AND CANCER SUSCEPTIBILITY - A REVIEW

Up to 90% of all cancers are possibly caused by environmental factors, such as tobacco smoke, diet and occupational exposures. The majority of chemical carcinogens require metabolic activation before they inter act with cellular macromolecules and can cause cancer initiation. The xenobiotic-metabolising machinery contains two main types of enzymes: the phase-I cytochromes P-450 (CYP) mediating oxidative metabolism, an d phase-II conjugating enzymes. Several phase-I and phase-II genes hav e recently been cloned and identified in humans. Many of them show pol ymorphism and have been suggested to contribute to individual cancer s usceptibility as genetic modifiers of cancer risk. Altered phenotypes and genotypes in the CYP subfamilies CYP1A1, CYP2D6 and CYP2E1 have be en associated with tobacco smoke-induced lung cancer and other cancers . Defective glutathione S-transferase (GST) and N-acetyltransferase (N AT) enzymes have been associated with an increased risk of developing lung and bladder cancer. There are also several studies in each catego ry in which no associations have been found, The risk of developing lu ng cancer is dramatically (up to 40-fold) elevated in subpopulations h aving simultaneously high-risk genotypes in CYP1A1 and GSTM1. There ar e several difficulties in this area of research. First, many of the ob served restriction-fragment length polymorphisms (RFLPs) are due to mu tations in introns or other silent areas of DNA, raising the possibili ty that any associations found between RFLPs and cancer occur only by chance. Second, biologically plausible mechanisms linking genotypes an d cancer are lacking in most of the observed cases, Third, substantial ethnic differences have been shown to exist in the distribution of de fective and functionally normal alleles, making extrapolations from on e ethnic group to another impossible. Thus, it is still difficult to s ay to what extent tests based on the polymerase chain reaction (PCR) a nd other methodology will be used to in the future to predict an indiv idual's susceptibility to cancers caused by xenobiotics.