EDAPT Altered Cellular Regulation Practice Test 2025 – Comprehensive Exam Prep

The potential effect of chromosomal alterations in cancer is primarily characterized by gene amplification, deletions, or translocations. In cancerous cells, these chromosomal changes can lead to significant disruptions in normal cellular functions.

Gene amplification results in an increased number of copies of a particular gene, which may enhance the production of proteins that promote cell growth and division, contributing to tumor development. Deletions of tumor suppressor genes remove crucial regulatory pathways that typically inhibit excessive cell growth and division. Translocations can lead to the fusion of genes that may create active oncogenes or dysregulate the expression of critical genes.

These alterations contribute to the hallmark traits of cancer cells, such as uncontrolled proliferation, resistance to apoptosis, and the ability to invade neighboring tissues. Thus, the presence of chromosomal alterations is a fundamental aspect of cancer biology that underscores the disease's complexity and aggressiveness.