The IR exists as two splice variant isoforms: the IR-B isoform that is responsible for signaling metabolic responses involved mainly in the regulation of glucose uptake and metabolism by increasing glucose transporter molecules on the plasma membrane of the insulin-responsive tissues muscle, liver, and fat, and the IR-A isoform, that is expressed in certain tumours (such as mammary cancers), signals predominantly mitogenic responses and is capable of binding IGF-II with high affinity [14, 15]. This evidence concerns the gene INSR and neoplasm.