Literally, a swelling; in the past the term has been used in reference to any swelling of the body, no matter what the cause. However, the word is now being used almost exclusively to refer to a neoplastic mass, and the more general usage is being discarded.
A neoplastic mass or neoplasm is a pathological lesion characterized by the progressive or uncontrolled proliferation of cells. The cells involved in the neoplastic growth have an intrinsic heritable abnormality such that they are not regulated properly by normal methods. The stimulus which elicits this growth is not usually known.
It is common to divide tumors into benign or malignant. The decision as to which category a tumor should be assigned is usually based on information gained from gross or microscopic examination, or both. Benign neoplasms usually grow slowly, remain so localized that they cause little harm, and generally can be successfully and permanently removed. Malignant or cancerous neoplasms tend to grow rapidly, spread throughout the body, and recur if removed. Not all tumors which have been classified as benign are harmless to the host, and some can cause serious problems. Difficulties may occur as a result of mechanical pressure.
The cells of benign tumors are well differentiated. This means that the cells are very like the normal tissue in size, structure, and spatial relationship. The cells forming the tumor usually function normally. Cell proliferation usually is slow enough so that there is not a large number of immature cells. As the cellular mass increases in size, most benign tumors develop a fibrous capsule around them which separates them from the normal tissue. The cells of a benign tumor remain at the site of origin and do not spread throughout the body. Anaplasia (loss of differentiation) is not seen in benign tumors.
The cells of malignant tumors may be well differentiated, but most have some degree of anaplasia. Anaplastic cells tend to be larger than normal and are abnormal, even bizarre, in shape. The nuclei tend to be very large, and irregular, and they often stain darkly. Malignant tumors may be partially but never completely encapsulated. The cells of the cancer infiltrate and destroy surrounding tissue. They have the ability to metastasize; that is, cells from the primary tumor are disseminated to other regions of the body where they are able to produce secondary tumors called metastases.
In most cases the formation of a neoplasm is irreversible. It results from a permanent cellular defect which is passed on to daughter cells. Tumors should undergo medical appraisal to determine what treatment, if any, is needed.
Tumor suppressor genes are a class of genes which, when mutated, predispose an individual to cancer. The mutations result in the loss of function of the particular tumor suppressor protein encoded by the gene. Although this class of genes was named for its link to human cancer, it is now clear that these genes play a critical role in the normal development, growth, and proliferation of cells and organs within the human body. The protein product of many tumor suppressor genes constrains cell growth and proliferation so that these events occur in a controlled manner. Thus, these genes appear to act in a manner antagonistic to that of oncogenes, which promote cell growth and proliferation.
The retinoblastoma (RB), p53, and p16 genes are the best-understood tumor suppressors. Inactivating mutations in the RB gene have been observed in retinoblastomas, osteosarcomas (cancer of the bone), as well as cancers of the lung, breast, and bladder. The p16 mutations have been observed in cancers of the skin, lung, breast, brain, bone, bladder, kidney, esophagus, and pancreas. The tumor suppressor p53 is the most frequently mutated gene associated with the development of many different types of human cancer, including those of the breast, lung, and colon. It is also associated with the rare inherited disease, Li-Fraumeni syndrome. Affected individuals manifest an increased likelihood of breast carcinomas, soft tissue sarcoma, brain tumors, osteosarcoma, leukemia, and adrenocortical carcinoma. Like RB and p16, p53 has a role in cell cycle regulation. In addition, p53 functions in the cell's decision on whether to undergo programmed cell death (apoptosis). Deregulaed cell proliferation and escape from apoptosis appear to be two common pathways leading to tumor formation. See also Cancer (medicine); Gene; Gene action; Mutation; Oncology; Tumor viruses.