There are two distinct types of
tumors: benign and malignant. Both types of tumors share a number of general characteristics, the broadest being that they are an abnormal
proliferation of cells. The main difference between the two types is what happens once the tumor has started growing. In a benign tumor, the proliferated cells stay in one location where they do not impact or spread to other surrounding tissues.
Malignant tumors, on the other hand, are capable of spreading throughout the entire body, causing new tumors to appear. This process is called
metastasis, and is a hallmark of cancerous tumors. In order to make sure that this cycle runs smoothly, there are a series of
checkpoints that the cell reaches to ensure that DNA replication has been completed correctly and that the cell is of correct size. These checkpoints include an un-replicated DNA checkpoint, a
spindle assembly checkpoint, a chromosome-segregation checkpoint, and various DNA damage checkpoints. Table 1 below describes different cell cycle checkpoints and their various purposes. In mammalian organisms, the cell cycle is regulated through interactions of
cyclin-dependent kinases (CDKs) and
cyclins.In the case of tumors, the cells display a level of abnormal growth. In most cases, this abnormal growth comes from an error in the cell cycle checkpoints. There are three general errors that occur within the cell cycle to cause abnormal cell growth. The first error is
unscheduled proliferation, essentially refers to the cell continuing to grow and divide without the proper signaling from mitosis. Genomic instability, the second error, refers to
mutations within the genome which causes errors in the replication or repair of the gene. Lastly, chromosomal instability is caused by mutations which disrupt the normal segregation of chromosomes in mitosis or meiosis. == Tumor growth in the stomach ==