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Slackers Cancer Molecular Biology Fact Stack

Date post: 24-Feb-2016
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Slackers Cancer Molecular Biology Fact Stack. Mike Ori. Disclaimer. These represent my understanding of the subject and have not been vetted or reviewed by faculty. Use at your own peril. I can’t type so below are common missing letters you may need to supply e r l - PowerPoint PPT Presentation
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Slackers Cancer Molecular Biology Fact Stack Mike Ori
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Page 1: Slackers Cancer Molecular Biology Fact Stack

Slackers Cancer Molecular Biology Fact Stack

Mike Ori

Page 2: Slackers Cancer Molecular Biology Fact Stack

Disclaimer

• These represent my understanding of the subject and have not been vetted or reviewed by faculty. Use at your own peril.

• I can’t type so below are common missing letters you may need to supply

• e r l• I didn’t use greek letters because they are a pain

to cut and paste in.

Page 3: Slackers Cancer Molecular Biology Fact Stack

• What are the key risk factors for colon cancer

Page 4: Slackers Cancer Molecular Biology Fact Stack

• Age• Genetics• Chronic bowel inflammation– Crohns– UC

• Diet

Page 5: Slackers Cancer Molecular Biology Fact Stack

• What are the two types of intestinal polyps

Page 6: Slackers Cancer Molecular Biology Fact Stack

• Hyperplastic– Smaller (< 5mm)– Better differentiation

• Adenomatous– Larger (>5mm)– Size and dysplasia correlate with disease risk– Increased malignant potential.

Page 7: Slackers Cancer Molecular Biology Fact Stack

• Outline the genetic steps required for the development of colon cancer

Page 8: Slackers Cancer Molecular Biology Fact Stack

• Epigenetic changes• Loss of growth control

– Loss of WNT signaling Pathway• APC is in WNT pathway

– RAS mutations• Increases MAP kinase• Increases PI3 kinase

– Loss of suppressors• TGF-B• P53• APC/B-catenin

• Genetic instability (?)– APC?

• Loss of apoptosis (?)– P53/B-catenin

Page 9: Slackers Cancer Molecular Biology Fact Stack

• What is the function of the WNT pathway

Page 10: Slackers Cancer Molecular Biology Fact Stack

• The WNT pathway controls growth of epithelial cells via the APC and B-catenin proteins.

Page 11: Slackers Cancer Molecular Biology Fact Stack

• Describe the interaction of APC and B-catenin

Page 12: Slackers Cancer Molecular Biology Fact Stack

• APC binds free B-catenin to prevent B-catenin from initiating transcription in the nucleus.

• B-catenin is a component of adherens junctions and may help to signal the completion of the epithelial layer. Presumably when B-catenin is present, the layer is incomplete and cell growth ensues to fill in the layer.

Page 13: Slackers Cancer Molecular Biology Fact Stack

• Describe the frequency of mutation of wnt and apc in sporadic cancers

Page 14: Slackers Cancer Molecular Biology Fact Stack

• Wnt pathway defective in 100%• APC defective in 70%

Page 15: Slackers Cancer Molecular Biology Fact Stack

• Describe the role of RAS in tumor development

Page 16: Slackers Cancer Molecular Biology Fact Stack

• RAS is a g-protein that leads to activation of downstream signaling pathways that lead proliferation

Page 17: Slackers Cancer Molecular Biology Fact Stack

• Describe the role of TGF-B in tumorgenesis

Page 18: Slackers Cancer Molecular Biology Fact Stack

• TGF-B normally halts the cell cycle in G1 to prevent proliferation and to activate differentiation or apoptosis.

• Loss of TGF-B allows for uncontrolled growth

Page 19: Slackers Cancer Molecular Biology Fact Stack

• What are the two forms of hereditary colon cancer

Page 20: Slackers Cancer Molecular Biology Fact Stack

• Familial adenematous polyposis (FAP)• Hereditary non-polyposis colorectal cancer

(HNPCC)

Page 21: Slackers Cancer Molecular Biology Fact Stack

• Why do molecular biologists make bad football coaches

Page 22: Slackers Cancer Molecular Biology Fact Stack

• Because their “simplified” playbook looks like this

Page 23: Slackers Cancer Molecular Biology Fact Stack

• What are the two types of genetic instability found in colon cancer

Page 24: Slackers Cancer Molecular Biology Fact Stack

• Chromosomal instability• Microsatellite instability

Page 25: Slackers Cancer Molecular Biology Fact Stack

• What is the failure of microsatellite instability

Page 26: Slackers Cancer Molecular Biology Fact Stack

• MIN results from failure of the mismatch repair mechanism

Page 27: Slackers Cancer Molecular Biology Fact Stack

• What is the failure in chromosomal instability

Page 28: Slackers Cancer Molecular Biology Fact Stack

• CIN results from defects in chromosomal segregation.

Page 29: Slackers Cancer Molecular Biology Fact Stack

• Relate FAP and HNPCC to MIN and CIN

Page 30: Slackers Cancer Molecular Biology Fact Stack

• FAP – CIN– APC gene

• HNPCC– MIN– MSH2, MLH1, PMS2 genes

Page 31: Slackers Cancer Molecular Biology Fact Stack

• How many mutations are likely involved in the transformation to malignancy

Page 32: Slackers Cancer Molecular Biology Fact Stack

• 5-6 mutations

Page 33: Slackers Cancer Molecular Biology Fact Stack

• Draw a sample timeline and gene pathway leading to malignancy

Page 34: Slackers Cancer Molecular Biology Fact Stack
Page 35: Slackers Cancer Molecular Biology Fact Stack

• List the major types of diagnostic errors

Page 36: Slackers Cancer Molecular Biology Fact Stack

• Differentiate retrospective vs prospective thinking

Page 37: Slackers Cancer Molecular Biology Fact Stack

• Retrospective thinking such that used in CPC’s and by novice examiners relies on broad spectrum data collection with analysis performed late in the process.

• Prospective thinking modifies the hypothesis during the data gathering process as a result of the collected data. This in turn modifies the data collection process.

Page 38: Slackers Cancer Molecular Biology Fact Stack

• What is a heuristic

Page 39: Slackers Cancer Molecular Biology Fact Stack

• Choose the correct answer• A statue of a bull commonly found in Minoan

culture• A small fluid filled cyst that forms as a result of

falling on the coccyx. • A problem solving technique that emphasizes

experience

Page 40: Slackers Cancer Molecular Biology Fact Stack

• What are common pitfalls of heuristics

Page 41: Slackers Cancer Molecular Biology Fact Stack

• Availability– Ease of recall

• Anchoring– Initial impressions

• Framing effects– How the problem is framed affects the thinking process

• Blind obedience– Remember authority figures are in charge, not all

knowledgeable

Page 42: Slackers Cancer Molecular Biology Fact Stack

• Why are mistakes by clinicians often unrecognized

Page 43: Slackers Cancer Molecular Biology Fact Stack

• Happen in distant past• Not recognized as mistakes by provider• PT does not return to same provider

Page 44: Slackers Cancer Molecular Biology Fact Stack

• What is the role of follow-up in clinical practice

Page 45: Slackers Cancer Molecular Biology Fact Stack

• Provides space and time• Additional data collection (tests)• Research• Trial therapy results

Page 46: Slackers Cancer Molecular Biology Fact Stack

• Who is responsible for test follow-up?

Page 47: Slackers Cancer Molecular Biology Fact Stack

• You ordered it, you own it.

Page 48: Slackers Cancer Molecular Biology Fact Stack

• What are the three stages of memory?

Page 49: Slackers Cancer Molecular Biology Fact Stack

• Encoding– Attending to the event

• Storage– Saving it for later

• Recall– Getting it back out

Page 50: Slackers Cancer Molecular Biology Fact Stack

• Describe the ability of the mind to process conceptual vs factual information

Page 51: Slackers Cancer Molecular Biology Fact Stack

• The mind is good at storing the concept (gist) of a set of facts but is relatively poor at storing the facts.

• An interesting aside, computers in contrast are very good at storing facts but not relating them conceptually.

Page 52: Slackers Cancer Molecular Biology Fact Stack

• Define impression management

Page 53: Slackers Cancer Molecular Biology Fact Stack

• The activities we undertake to control the impressions others have of ourselves.

Page 54: Slackers Cancer Molecular Biology Fact Stack

• Define self-enhancement

Page 55: Slackers Cancer Molecular Biology Fact Stack

• Performing actions intended to bolster the positive impression others have of us.

• Giving money to the poor, performing pro bono work

Page 56: Slackers Cancer Molecular Biology Fact Stack

• Define self verification

Page 57: Slackers Cancer Molecular Biology Fact Stack

• Understanding the impression others have of us and relating that back to how we see ourselves. Ideally the two will match.

Page 58: Slackers Cancer Molecular Biology Fact Stack

• Which type of shock is dobutamine most useful and why

Page 59: Slackers Cancer Molecular Biology Fact Stack

• Dobutamine is a B1 agonist (weak B2) that is useful in cardiogenic shock because it increase rate and force of contraction

Page 60: Slackers Cancer Molecular Biology Fact Stack

• Describe the role of dopamine in shock

Page 61: Slackers Cancer Molecular Biology Fact Stack

• Useful in cardiogenic shock.• Interacts with dopaminergic receptors to

vasodilate mesenteric and renal arterioles thus increasing renal perfusion.

• At moderate levels it acts as a B2 and at high levels it acts as an a1 agonist

Page 62: Slackers Cancer Molecular Biology Fact Stack

• What is the role of phenylephrine in shock

Page 63: Slackers Cancer Molecular Biology Fact Stack

• Phenylephrine is a a1 agonist that is sometimes used in septic shock as a pressor.

Page 64: Slackers Cancer Molecular Biology Fact Stack

• What is the role of epi and NE in hypovolemic shock

Page 65: Slackers Cancer Molecular Biology Fact Stack

• Relatively little. The body usually has tremendous sympathetic outflow as a result of the shock state and trauma and thus has plenty of epi/ne circulating.

Page 66: Slackers Cancer Molecular Biology Fact Stack

• What are the expected values for cardiac output, left ventricular end diastolic volume, and mixed venous O2 in hypovolemic, cardiogenic, and septic shock

Page 67: Slackers Cancer Molecular Biology Fact Stack

Output LVEDV/wedge MVO2 SVR

Hypovolemic Low Low Low High

Cardiogenic Low High Low High

Septic High Normal? High Low

Page 68: Slackers Cancer Molecular Biology Fact Stack

• What physical findings are present in metabolic syndrome

Page 69: Slackers Cancer Molecular Biology Fact Stack

• Impaired glucose tolerance• Obesity• Hyperlipidemia• Hypertension

Page 70: Slackers Cancer Molecular Biology Fact Stack

• How does metabolic susceptibility relate to metabolic syndrome

Page 71: Slackers Cancer Molecular Biology Fact Stack

• Metabolic susceptibility is believed to be a necessary component in the development of metabolic syndrome. Its presence is inferred because some similar individuals do not progress to metabolic syndrome.

Page 72: Slackers Cancer Molecular Biology Fact Stack

• What role do fatty acids play in the development of insulin resistance

Page 73: Slackers Cancer Molecular Biology Fact Stack

• Chronically elevated fatty acids induce insulin resistance by increasing the availability of substrates that alter down-stream signaling.

• Specifically, excess NADH and acetyl-CoA disrupt pyruvate dehydrogenase to effectively cutoff the use of glucose as a fuel.

Page 74: Slackers Cancer Molecular Biology Fact Stack

• What is the role of adiponectin in metabolic syndrome?

Page 75: Slackers Cancer Molecular Biology Fact Stack

• Adiponectin is an anti-inflammatory cytokine that decreases in obesity. One of its roles is to decrease lipogenesis. Thus obese individuals have an increased tendency to lipogenesis.

Page 76: Slackers Cancer Molecular Biology Fact Stack

• What is the role of resistin in metabolic syndrome

Page 77: Slackers Cancer Molecular Biology Fact Stack

• Resistin is an autocrine factor that protects full adipocytes. In metabolic syndrome the large number of full adipocytes causes resistin to take on a more systemic effect wherein it begins to affect muscle cells.

Page 78: Slackers Cancer Molecular Biology Fact Stack

• Describe the role of insulin, TNF-a, and IL-6 in VLDL synthesis

Page 79: Slackers Cancer Molecular Biology Fact Stack

• VLDL is synthesized in the liver. Both TNF-a and IL-6 increase its synthesis and both are increased in obesity. Normally, insulin would activate lipoprotein lipase in the periphery to encourage the uptake of the fatty acids in the VLDL but in insulin resistance, this action is diminished. Thus, the body creates more VLDL’s than usual but they are not degraded. As the levels of VLDL increase some will be broken down; resulting in increased LDL.

Page 80: Slackers Cancer Molecular Biology Fact Stack

• Describe the role of insulin in liver of metabolic syndrome

Page 81: Slackers Cancer Molecular Biology Fact Stack

• Insulin normally promotes the mobilization of glucose transporters to the membrane, the conversion of glucose to glycogen, and the conversion of acetyl-coa to fatty acids. With insulin resistance, glucose uptake and glycogenolysis are both impaired.

Page 82: Slackers Cancer Molecular Biology Fact Stack

• Explain the origin of the prothrombotic state associated with diabetic patients

Page 83: Slackers Cancer Molecular Biology Fact Stack

• Excess production of TNF-a and IL-6 coupled with a decrease in adiponectin leads to an inflammatory state. This in turn causes the liver to synthesize more fibrinogen and plasminogen activator inhibitor 1.

Page 84: Slackers Cancer Molecular Biology Fact Stack

• List the management goals for diabetic patients

Page 85: Slackers Cancer Molecular Biology Fact Stack

• A1C < 7%• LDL < 100• Systolic BP < 130

Page 86: Slackers Cancer Molecular Biology Fact Stack

• List the macronutrient proportions for patients with diabetes

Page 87: Slackers Cancer Molecular Biology Fact Stack

• CHO = 50%• Fat = 30%• Protein = 20%

Page 88: Slackers Cancer Molecular Biology Fact Stack

• What are the common receptors used in the prognosis and treatment of breast cancer

Page 89: Slackers Cancer Molecular Biology Fact Stack

• Estrogen receptor• Progesterone receptor• Her2/Neu/ErbB2

Page 90: Slackers Cancer Molecular Biology Fact Stack

• What is a gatekeeper

Page 91: Slackers Cancer Molecular Biology Fact Stack
Page 92: Slackers Cancer Molecular Biology Fact Stack

• Seriously, what is a gatekeeper

Page 93: Slackers Cancer Molecular Biology Fact Stack

• A gene that acts by directly suppressing cell proliferation

Page 94: Slackers Cancer Molecular Biology Fact Stack

• What is a caretaker

Page 95: Slackers Cancer Molecular Biology Fact Stack

• A gene that functions to maintain genenome stability

Page 96: Slackers Cancer Molecular Biology Fact Stack

• Is BRCA1/2 a gatekeeper or caretaker

Page 97: Slackers Cancer Molecular Biology Fact Stack

• Caretaker

Page 98: Slackers Cancer Molecular Biology Fact Stack

• What is the function of BRCA1/2

Page 99: Slackers Cancer Molecular Biology Fact Stack

• They are involved in homology directed repair of DS DNA breaks

Page 100: Slackers Cancer Molecular Biology Fact Stack

• What attributes are beneficial for screening and diagnostic tests

Page 101: Slackers Cancer Molecular Biology Fact Stack

• Screening tests need to be cheap, quick, easy, and sensitive. They do not have to be very specific.

• The ideal diagnostic tests need to be sensitive and specific. If they aren’t sensitive then they at least need to be specific.

• Is a home pregnancy test a screening or a diagnostic test?

Page 102: Slackers Cancer Molecular Biology Fact Stack

• What are the common viruses associated with cancer.

Page 103: Slackers Cancer Molecular Biology Fact Stack

HIV action

HTLV1 Adult T-cell leukemia None listed

HPV Squamous cell carcinomas Viral escape via immune suppression

EBV Lymphomas Co factor

HBV Hepatocellular carcinoma None listed

HCV Hepatocellular carcinoma None listed

KSV Kaposi sarcoma Cofactor via cytokines

HIV Lymphoma, SCC, Body cavity lymphoma, primary CNS lymphoma, kaposi

Page 104: Slackers Cancer Molecular Biology Fact Stack

• What are the molecular events leading to cancer from viruses

Page 105: Slackers Cancer Molecular Biology Fact Stack

HTLV1 TAX gene drives replication. /\ cyclin D, /\ NF-kappa-B

HPV Viral E6 and E7 interfere with P53 and P21

EBV Viral LMP1 acts like CD40 ligand to drive proliferation, viral EBNA2 /\ cyclin D, Viral IL10 prevents macrophage activation of T-cells

HBV No oncogenes. Chronic inflammation

HCV No oncogenes. Chronic inflammation

KSV Viral VEGF. P53 suppression. Viral cyclin D analogue

HIV

Page 106: Slackers Cancer Molecular Biology Fact Stack

• Differentiate descriptive and inferential statistics

Page 107: Slackers Cancer Molecular Biology Fact Stack

• Descriptive– Describe qualities about the data but cannot be

used to infer

• Inferential– Can be used to draw conclusions

Page 108: Slackers Cancer Molecular Biology Fact Stack

• Define nominal and ordinal data

Page 109: Slackers Cancer Molecular Biology Fact Stack

• Nominal– Data described by labels of no numerical significance. – Numerical operations are not possible even if the data appear to be

numeric. For instance, the subtraction of two zip codes has no meaning.• Only mode has meaning

• Ordinal– A rank ordered category such as least to most, worst to best, pain levels,

satisfaction, etc– There is intrinsic order but the value between each item is variable. For

instance, what is the quantitative difference between somewhat satisfied and satisfied.

– Some numerical operations are allowed• Mode and median have meaning

Page 110: Slackers Cancer Molecular Biology Fact Stack

• Describe the types of metric data

Page 111: Slackers Cancer Molecular Biology Fact Stack

• Physical measurement or counting• All numerical operations are allowed– Mode– Median– Mean

• Variable has equal intervals between values.• Interval– Metric data with an arbitrary zero

• Ratio– Metric data with a meaningful 0

Page 112: Slackers Cancer Molecular Biology Fact Stack

• What is the worst statistical error type, type I or type II

Page 113: Slackers Cancer Molecular Biology Fact Stack

• Type I is worst– Reject the null hypothesis (H0) even though its

true. So we found something that isn’t there. In other words, we’ll treat with snake oil.

• Note that type II accepts the null hypothesis even though its false. Thus we will withhold a useful treatment because we fail to recognize that it is useful.


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