NRS 313 Study Guide - Final Guide: Chromone, Cervical Cancer, Cell Growth

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Cancer and Genetics: Essential Concepts
Tumors
o Benign
Grow slowly
Well-differentiated
Encapsulated
Non-invasive
Do not metastasize
Ex: moles or uterine fibroids
Endothelial cells are under the control of estrogen. When
progesterone is higher these cells thicken. Sometimes we get a
benign tumor here. Cell growth signals are dysfunctional. If they
want to conceive, these can be a cause for infertility.
o Carcinoma in situ:
early stages of growth
Localized
No penetration of BM=basement membrane
Layer of cells between specialized tissue
Well defined
No metastasis and encapsulated
o Malignant= cancer is progressing
Fast growing
Poorly differentiated : (anaplasia)
Not a specialized cell anymore
Not encapsulated
Invasive
Spreads (metastasizes) to other tissues via blood stream or lymphatics
Malignant vs. Benign tumors
o Benign (Not cancer) tumor cells grow only locally an cannot spread by invasive
or metastasis
o Malignant( Cancer) cells invade neighboring tissues, enter blood vessels, and
metastasize to different sites
o Contact Inhibition: When cells come in contact, their growth stops
o Angiogenesis: blood vessel formation
o Protease: made by cancer cells to cut through proteins
o Autocrine signaling: communicates to itself to replicate
o Telomerase: telomere caps protect ends of chromosomes. Cancer cells make their
own. Allows for the cancer cells to become invincible.
o Shrouded in own platelets: surrounded by fibrin mesh that allows for the cells
to go undetected, Natural killer cells cant find the cancer cells.
Genetic Basis for Cancer
o Cancer incidence increases with age and exposure to carcinogens
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o Genetic instability
genetic instability is often considered a hallmark of cancer.
Mutations in DNA of gametes (male or female germ cell) is passed on to
offspring
o Genetic inheritance
50% inheritance rate with dominant gene
25% inheritance rate with recessive gene
o A culmination of genetic mutations over time
Combined effect of genetics plus environment
One or two mutations is not enough to cause cancer
Tumor suppressor genes should “eliminate” cells that have DNA
mutations
Mutations
o Mutations are relatively rare:
DNA polymerase: Proofreads the code and corrects errors
If it notices a significant mismatch it will stop the replication
Important for inhibiting cancer
Tumor suppressor genes: detect errors and schedule the cell for
apoptosis
o BRACA 1 and 2: in females we see an increase in breast and ovarian cancer if
these TSGs are mutated. In males we see prostate and colon cancer.
These are dominant mutations
o P53: guardian of the genome. Strong tumor suppressor gene. Targets cells for cell
death
o Base pair substitution : still results in a good protein sequence
(mis-sense mutation): Silent mutation. We don’t get the same replication
One pair of bases are substituted for another within one codon
The dog saw the car and ran.
The dog saw the cat and ran.
o Frameshift substitution: results in a faulty and/or dysfunctional protein
sequence
One or more pairs of bases are either deleted (missing pair) or inserted
changing the sequence of codons
hed ogs awt hec ata ndr ant. (Non-sense mutation)
changes entire amino acid combination
Chromosomes
o DNA is coiled tightly around protein molecules forming chromatin
o When cell divides, chromatin condense into structures called chromosomes
o Somatic Cells have 23 pairs of chromosomes (Thus, 46 chromosomes), one of
each pair from mother and one from father. These are diploid cells.
o Gametes cells have half of each pair (thus, 23 chromosomes). These are haploid
cells
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Document Summary

Cancer and genetics: essential concepts: tumors, benign, grow slowly, well-differentiated, encapsulated, non-invasive, do not metastasize, ex: moles or uterine fibroids, endothelial cells are under the control of estrogen. If it notices a significant mismatch it will stop the replication. Important for inhibiting cancer: tumor suppressor genes: detect errors and schedule the cell for apoptosis, braca 1 and 2: in females we see an increase in breast and ovarian cancer if these tsgs are mutated. In males we see prostate and colon cancer: these are dominant mutations, p53: guardian of the genome. Targets cells for cell death: base pair substitution : still results in a good protein sequence (mis-sense mutation): silent mutation. These are diploid cells: gametes cells have half of each pair (thus, 23 chromosomes). These are haploid cells: chromosomes normally split. Chronic diabetes can be related to infertility: trisomy at chromosome 21=> down syndrome, non dysjunction error during neosis.

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