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Dysplasia
disordered growth can result from hyperplasia and metaplasia
Neoplasia
new growth due to mutations
Benign suffix
oma
Malignant suffix
often end in carcinoma or sarcoma
Benign neoplasm
no ability to invade surrounding cell
Malignant neoplasm
ability to invade surrounding tissue and metastasize to other locations
Hamartoma
Disorganized mass of tissue normally found at the location
Choristoma
Disorganized mass of tissue not normally found at the location
Carcinoma
Malignant neoplasm derived from epithelial cells
Sarcoma
Malignant neoplasm derived from mesenchymal cells (e.g., bone, cartilage, skeletal muscle)
Lymphoma/Leukemia
Malignant neoplasm derived from lymphocytes/hematopoietic cells
Melanoma
Malignant neoplasm derived from melanocytes
Teratoma
Neoplasm derived from germ cell layers; usually all three layers (ectoderm, mesoderm and endoderm)
Mixed tumor
Most often applies to germ cell tumors, with more than one component (e.g., choriocarcinoma mixed with embryonal carcinoma); also pleomorphic adenoma
Neoplasia Grade or differentiation
How similar to the cell type of origin the tumor is, subjective
Neoplasia STAGE
Based upon T (tumor characteristics), N (lymph node involvement), and M (metastatic) objective, stage I- IV
Features of anaplasia
such degree of hyperchromasia (increased intensity of chromatin staining), pleomorphism (variation in size and shape of cell and/or nucleus), abnormal mitotic figures that cells do not look at all like their cell of origin
Main forms of carcinoma
squamous cell carcinoma and adenocarcinoma
Burkitt's lymphoma
right lower quadrant and jaw- EBV
Dysplasia vs carcinoma in situ vs carcinoma
all Hyperchromasia, pleomorphism; increased mitotic rate; carcinoma in situ is full thickness of mucosa with no invasion of submucosa, carcinoma invades sub mucosa
CIN1
cervical intraepithelial neoplasia
Incidence
how many new people develop tumor in year
Prevalence
how many people with a tumor are present in population
High prevalence compared to incidence
less aggressive tumor, many people have it and aren't dead
Pathways of neoplastic spread
lymphatic or blood
Sarcoma spread by
blood
Carcinoma spread by
lymphatic
Key regulators of cell cycle
p16, cyclin D, CDK4, RB
Cyclin D and CDK4
promote cycle cycle division, g1 to s
P16 function
inhibits cycle cycle division, g1 to s
NOTCH1 gene
tumor suppressor gene in squamous cell carcinoma, promotes growth in T-cell leukemia
microRNA
negative regulator of genes (block translation)
Tumor suppressor genes
must lose both genes! normal function inhibit cell growth, abnormal- promotes cell division
Proto-oncogenes
just one will cause cancer, normal- promote cell growth and division
Growth factor receptors
ERBB1 (EGF receptor) ERBB2 (HER2—breast cancer)
Downstream signal-transducing proteins
RAS
Tumor suppressor genes
RB, CDKN2A, p53, TGF-beta, E-cadherin, beta-cadherin
Cancer related to RB
retinoblastoma
Cancer related to CDKN2A
melanoma
Cancer related to E-cadherin
NF2-meningioma
Cancer related to beta-cadherin
APC-colon carcinoma
P53 job
arrests cell cycle and activates apoptosis (bax)
Hereditary non-polyposis colon carcinoma
defect in DNA mismatch repair genes
Xeroderma pigmentosa
defect in nucleotide excision repair system that repairs damage from UV light
Ataxia-telangiectasia
mutation in gene that senses DNA damage
BRCA1/BRCA2
prone to chromosomal breaks
Retinoblastoma Gene and tumor
RB, retinoblastoma
Li-Fraumeni Gene and tumor
p53, many tumors
Melanoma Gene and tumor
CDKN2A, melanoma
Familial adenomatous polyposis Gene and tumor
APC, colon carcinoma
Neurofibromatosis I and II Gene and tumor
NF1 and NF2, plexiform neurofribroma/ meningioma
Multiple endocrine neoplasia Gene and tumor
MEN1 and RET
Hereditary non-polyposis colon cancer genes
MSH2, MLH1, MSH6
Nevoid basal cell carcinoma Gene and tumor
PTCH1 and basal cell carcinoma
Associated cancer with inflammatory bowel disease
colon cancer
Associated cancer with lichen sclerosis
vulvar squamous cell carcinoma
Associated cancer with Hashimoto's thyroiditis
MALT lymphoma
Associated cancer with chronic cystitis
squamous cell carcinoma of bladder, caused by schistosomiasis
Beta-naphthylamine neoplasm
bladder cancer Aflatoxin B1 exposure and neoplasm
Vinyl chloride neoplasm
angiosarcoma of liver
Radiation (UV light, radiographs, radionuclides) neoplasm
Leukemia, thyroid, breast, colon; papillary thyroid carcinoma; skin cancer
HPV neoplasm
Cervical and oropharyngeal squamous cell carcinoma
Epstein-Barr virus neoplasm
burkitt lymphoma
Hepatitis B and C neoplasm
hepatocellular carcinoma
Helicobacter pylori
monoclonal b-cell tumor (MALToma)
Asbestos neoplasm
mesothelioma
Benzene neoplasm
acute myeloid leukemia
Radon neoplasm
lung carcinoma
Cachexia
marked weight loss associated with neoplasm Paraneoplastic syndromes
SIAHD paraneoplastic mechanism and tumor
Anti-diuretic hormone Small cell carcinoma of lung
Hypercalcemia paraneoplastic mechanism and tumor
Parathyroid hormone related peptide Squamous cell carcinoma of the lung (Others
Polycythemia paraneoplastic mechanism and tumor
Erythropoietin Renal cell carcinoma; cerebellar hemangioblastoma; hepatocellular carcinoma
Myasthenia paraneoplastic mechanism and tumor
Immunologic Bronchogenic carcinoma; thymoma
Acanthosis nigricans paraneoplastic mechanism and tumor
Immunologic Gastric carcinoma (others
Hypertrophic osteoarthropathy paraneoplastic mechanism and tumor
Unknown Bronchogenic carcinoma
Trousseau syndrome (migratory venous thrombosis) paraneoplastic mechanism and tumor
Mucin production Pancreatic carcinoma
Clonality
neoplasm derived from a single cell, clones of original tumor cell
Two-hit hypothesis
Examplkes of growth signals
growth factors, growth factor receptors, cyclin dependent kinases
Insensitivity to growth inhibitopry signals
shut down tumor suppressor genes/affect contact inhibition
Examples of growth inhibitory signals
RB, p53 (tumor supressors), NF2/APC (contact inhibition)
Self sufficiency growth factor signals Growth factor receptor examples
ERBB1 (egf receptor) ERBB2 (her2 breast cancer)
RB
tumor suppressor gene in retinoblastoma
CDKN2A
tumor suppressor gene in melanoma
P53
tumor suppressor gene in most cancers
E-cadherin
tumor suppressor gene NF-2 meningioma
B-cadherin (WNT pathway)
tumor suppressor gene in APC-colon carcinoma