Biochemistry of Leukemia Flashcards

1
Q

tumor lysis syndrome

A

occurs when large amounts of tumor cells lyse at once
-can be secondary to chemotherapy
-can be spontaneous when tumor outgrows its vascular support

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2
Q

Na+/K+ ATPase

A

-maintains proper osmotic balance
-uses between 30-75% of cellular ATP

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3
Q

inhibition of Na+/K+ ATPase

A

osmotic balance shifts and water flows into cells and they burst

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4
Q

metabolic derangements seen in tumor lysis syndrome

A

hyperkalemia, hypocalcemia, hyperuricemia, hyperphosphatemia, high LDH

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5
Q

HYPERkalemia and tumor lysis syndrome

A

-cells normally concentrate potassium
-many tumor cells lysing is delivering a potassium load to the blood

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6
Q

HYPERphosphatemia and tumor lysis syndrome

A

-cells are high in phosphates (think of all the phosphorylated NTPs and every nucleotide in the genome is linked by a phosphodiester bond), so cell lysis would release a lot of phosphate

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7
Q

HYPOcalcemia and tumor lysis syndrome

A

calcium cross-precipitates with phosphate, so calcium goes down (calcium-phosphate crystals)

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8
Q

HYPERuricemia and tumor lysis syndrome

A

uric acid is a breakdown product of purines, and each tumor cell contains 3 billion nucleotides, so lysis of the cell causes excessive purine breakdown and therefore high uric acid

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9
Q

elevated LDH (lactate dehydrogenase) and tumor lysis syndrome

A

-takes the product of glycolysis, pyruvate, and converts it to lactate
-consumes NADH and generates NAD+ to keep glycolysis going
-causes elevated lactate levels

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10
Q

acute kidney injury and tumor lysis syndrome

A

excess uric acid forms crystals and clogs the kidneys, causing urate crystal nephropathy

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11
Q

solubility of urate

A

-urate is not soluble above physiologic levels
-acidic environment in distal tubules and collecting ducts promotes crystal formation
-worse is that calcium-phosphate crystals increase the formation of urate crystals and vice versa

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12
Q

tumor lysis syndrome prophylaxis

A

1) IV fluids (promotes clearance of metabolites)
2) allopurinol (competitive inhibitor of xanthine oxidase, inhibiting the production of urate; does not treat the crystals already formed though)

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13
Q

treatment of urate crystals

A

rasburicase (converts uric acid to a more soluble form so it can be excreted in the urine)

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14
Q

hydrea and cytoreduction

A

inhibits ribonucleotide reductase, which stops DNA synthesis, arresting the cell in S phase

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15
Q

ribonucleotide reductase

A

enzyme that catalyzes the conversion of ribonucleotides to deoyxribonucleotides, acting as the rate-limiting step in DNA synthesis; ensures a balance of the deoxyribonucletides
-active when ATP levels are HIGH
-inactive when dATP levels are high

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16
Q

cytarabine treatment

A

a cytidine analogue that is S-phase specific; incorporates into the newly made DNA and blocks addition of any more nucleotides; given continuously because we need to catch cells that are actively replicating
*used as chemotherapeutic tx

17
Q

daunorubicin treatment

A

inhibits topoisomerase II (which resolves supercoils); not specific to S phase, so given by bolus

18
Q

midostaurin treatment

A

a tyrosine kinase inhibitor; blocks ATP binding to the kinase, so the mutated kinase cannot continue to phosphorylate its targets

19
Q

after a bone marrow transplant, blood from the patient would have the (donor/recipient?) karyotype

A

blood would have the DONOR’s karyotype; so if recipient is male and donor is female, then the blood sample would show a female karyotype (46, XX), even though the other cells in his body would be 46, XY