Cancer Biology Flashcards
(48 cards)
Adenomatous Polyposis Coli (APC)
A dominant tumor suppressor gene on chromosome 5. Mutations of APC are associated with familial adenomatous polyposis or FAP.
Anaplasia
Loss of normal shape and organization of cells and tissues associated with malignant transformation.
Adenocarcinoma
Cancers of glandular epithelial cells.
Anemia
Reduction in the number of red blood cells, often causing fatigue.
Anorexia
Loss of appetite.
Benign
Non-cancerous.
Benign Tumors
Non-cancerous tumors.
Blood Dyscrasias
An imbalance of the cellular components of the blood.
BRCA-1
A dominant caretaker gene on chromosome 17 that reports damaged DNA. BRCA-1 mutations are found in about 7% of women with a history of breast cancer.
BRCA-2
A dominant caretaker gene on chromosome 13 that repairs damaged DNA. BRCA-1 and 2 mutations are responsible for about 5-10% of all breast cancers.
Cachexia
General physical wasting and malnutrition associated with chronic disease.
Cancer
Any neoplasm that demonstrates uncontrolled growth of abnormal cells and is associated with invasive spread and metastasis.
Carcinoma
Cancers of squamous epithelial cells.
Carcinoma In Situ (CIS)
The earliest stage in development of carcinomas when cancer cells have not spread beyond their immediate site of origin, as when epithelial cells have not yet invaded through the basement membrane of their extracellular cell matrix.
Caretaker Genes
Genes that produce the proteins that repair damaged DNA.
Cellular Proto-Oncogenes (c-onc)
Any of at least 50 different genes in the human genome such as ras that are expressed during the cell growth cycle. Cancer of a cell is usually the result of multiple mutations in c-onc genes.
Differentiation
The process of anatomic and functional maturation demonstrated by normal cells and tissues. Progressively more undifferentiated malignancies are more primitive, under less genetic regulatory control, and are more aggressive.
Ductal Carcinoma In Situ (DCIS)
The pre-invasive stage of breast duct cell cancer.
Dysplasia
Abnormally appearing cells usually of squamous epithelium considered to be a pre-malignant change.
Erythrocytes
Red blood cells.
Familial Adenomatous Polyposis (FAP)
A familial form of colon cancer caused by mutations of the APC gene, characterized by development of thousands of polyps of the colon resulting in colon cancer before the third of fourth decade of life.
Five-Year Survival
The customary method of describing prognosis as the percent likelihood that an individual with a cancer of a specific stage and grade will be alive in five years.
Hereditary Non-Polyposis Colon Cancer (HNPCC) (“Lynch Syndrome”)
Colon cancer associated with mutations of any of five different genes on chromosomes 2, 3, and 7 that comprise 5-15% of all cases of colon cancer.
Homologous Replication
DNA repair accomplished by certain caretaker genes by copying the correct (non-mutated) nucleotide(s) from another homologous trang, either in the other chromosome, a sister compound, or homologous repeat sequences on the same chromosome.