Exam 2 Flashcards
Malignant
capable of metastasis
tumor
a non-specific term meaning lump or swelling
metastasis
discontinuous spread of malignant neoplasm
neoplasm
uncontrolled growth of cells
cancer
any malignant tumor/neoplasm
carcinoma in situ (CIS)
- cancer in place
- has not through basement membrane yet
- if caught in this stage it can be cut out to cure it
TNM system
- describes staging
- T: describes tumor (0-3)
- N: lymph nodes (0-2)
- M: metastasis (0-2)
staging
describes extent of spreed
Dysplasia
- premalignant state
- if it stays there it will become cancer
- doesn’t necessarily progress to malignancy
- usually occurs in the epithelium
carcinogenesis
the creation of cancer
cachexia
generalized wasting that occurs in terminal cancer
grading of tumor
- shows how differentiated or undifferentiated cells are
- degree of differentiation roughly estimates tumors malignant potential
CAUTION
- Changes in bowel/bladder habits or functions
- A sore that doesn’t heal
- Unusual bleeding or discharge
- Thickening or lump in breast or elsewhere
- Indigestion or difficulty swallowing
- Obvious changes in a wart or mole
- Nagging cough or horseness
lifestyle choices that reduce risk of cancer
- don’t use tobacco
- sun safely
- diet (processed foods are carcinogens)
- drink alcohol moderately
- exercise regularly
- vaccinations (HPV)
- safe sex practices
- maintain a healthy weight
- self-examinations
what is the most deadly cancer in adults?
lung cancer
which cancer is the most common in women?
breast cancer
which cancer is the most common in men?
prostate cancer
proto-oncogene
a normal gene
oncogene
- mutated proto-oncogene
- “green light”
KRAS oncogene
- mutation of the RAS proto-oncogene
- mutated RAS leads to activation of protein which stimulates transcription
- mutation in RAS causes it to always be “on” making cells grow really fast
tumor suppressor genes
- they detect and repair DNA damage before they can go through mitosis
- “red light”
mutation of Tumor Suppressor p53
- mutation causes the levels of p53 to increase in a cell
- results in:
1. ) recruit in DNA repair
2. ) senescence
3. ) death by apoptosis
what is the most mutated tumor suppressor gene?
p53
what is the function of tumor suppressor gene p53
stops the cell cycle and usually found in low amount in cells
senescence
the cell is still alive but it will never divide again
how is cancer a multi-hit development?
in order for cancer to acquire a malignant phenotype it needs to have multiple mutations (hits) to genome
etiology of cancer
-cancer occurs due to mutations in DNA
what cells does cancer occur in
somatic or germ cells
why is cancer hard to treat?
each cancer is genetically unique, not everyone’s is the same
manifestations of cancer
- ) mass
- ) hormone production
- ) systemic manifestation
- ) cachexia
paraneoplastic syndrome
manifestation of aberrant and uncontrolled hormone production by a malignant neoplasm
EX: lung cancer produces unregulated cortisol, so it can be misdiagnosed as Cushings syndrome
Surgery for treating cancer
- prevent cancer
- cure depending on localization
- biopsy for diagnosis
- debulking surgery
- palliative surgery: surgery to manage symptoms
hormone therapy for cancer treatment
- activation or blockage of a receptor
- interferes with cellular growth and signaling
ionizing radiation for cancer treatment
-targets cells in S phase so mutated DNA can’t divide
goals:
-eradicate cancer without excessive toxicity
-avoid damage to normal structure
chemotherapy for cancer treatment
- given via IV
- chemicals target ALL rapidly dividing cells (can’t target only cancer dividing cells)
- puts a base analogue in DNA that won’t work
symptoms of chemotherapy
- hair loss
- low white blood cell count, can get sick more often
- low red blood cell count, anemia
- loss of appetite
immunotherapy
- immune system sees mutant cell as foreign
- it then stimulates own immune system to better recognize cancer cells
- tumor antibodies
targeted therapy
- “precession medicine”: acts on specific molecular targets
- EX: HER2
mammography
screening for breast cancer recommenced at age 40
pap smear
screening for cervical cancer
colonoscopcy/fecal occulta test
screening for colon cancer recommened at age 50
what cancers are the most deadly?
cancers that don’t have screening tests
congenital disease
a disease that you are born with
allele
variation form of a gene (EX: eye color)
Non-disjuction
DNA doesnt pull apart correctly in meiosis
Genetic disease
disease caused by abnormal DNA
Karyotype
illustration of chromosomes that is used to visualize them and look for abnormailites and alterations
Aneuploidy
when there is one or more extra or missing chromosomes which results in abnormal number
what are the main causes of developmental diseases?
1.) birth defects/congenital anomalies
how does a genetic disease develop?
- inherited by parents
- can occur in gamete development
fetal alcohol syndrome causes and effects
- Cause: when mom consumes alcohol during pregnancy
- effects: fetal growth restriction, CNS abnormalities, and distinctive facial features
what is Amniocentesis
- a sample of amniotic fluid is taken via needle to check for disease
- has risk for miscarriage
what is chorionic villi testing
- sample of projections (chorionic villi) of placenta are taken to test for disease
- greater risk for pregnancy loss
is Amniocentesis or CVT more accurate and why?
amniocentesis is more accurate because in CVT it takes samples of the placenta not direct samples of fetus
who is recommended to have amniocentesis or CVT done?
- mother 35 or older
- parents who have a child with genetic disease
- family history
Trisomy 21
- Down syndrome
- 3 21 chromosomes (extra)
- cause due to non-disjunction in mieosis 1
what are manifestations of down syndrome
- intellectual impairment that varie
- round face and slanted eyes
- small stature
- congenital heart defects
- intestinal defects
- increased risk for alzheimers
Turners syndrome
- sex chromosome abnormalities
- females only has 1 x (x)chromosome instead of 1
- causes: non disjunction
- features: short in stature, webbing at neck, secondary sex organ don’t develop, infertile/don’t through puberty
Kleinfelter syndrome
- sex chromosome abnormalitie
- male has extra x chromosome (xxy)
- causes: non disjunction
features: tall, long limbs, breast development, secondary sex organs don’t develop, infertile
Autosomal dominant inheritance
- disease is expressed if only one copy is present
- affected person has 50% of passing disease to off spring
Martan syndrome
- autosomal dominant disease
- effects: tall w long limbs and fingers/toes, heart valves don’t close correctly, eyes can detach from retinas, blood vessels more likely yo stretch, increase in cardiac death
autosomal recessive inheritance
- need two copies of genes
- both parents must be carriers
cystic fibrosis
- autosomal recessive disease
- most common ARD affecting white mothers
- causes mutation in chloride channels which regulates chloride and sodium movement
- effects: thick, sticky mucus that doesn’t move