size of detectable tumour
10^9 cells
1cm/1g
size of lethal tumour
10^12 cells
fractional cell kill hypothesis
each time chemotherapy dose is repeated, same proportion of cells, not same number, is killed
3 log kill, 1 log growth
parts of body where there is rapid proliferation
bone marrow
GI mucosa
ovary
testis
hair follicles
proliferative side effects of chemo
myelosuppression
immunosuppression
mucositis
GI disturbances
alopecia
gonadal damage
What are alkylating agents and how do they work?
what can alkylating agents bind to/form covalent bonds with? (nucleophiles)
Are alkylating agents cell cycle specific?
NO
purine bases
2 rings
adenine
guanine
pyrimidine bases
1 ring
cytosine
thymine
uracil
How are bases from 2 strands of DNA bonded?
H bonding
How many H bonds between A and T?
2
How many H bonds between C and G?
3
What type of bond does alkylating agent form with anything in body?
covalent bond
examples of nitrogen mustards used as chemo
cyclophosphamide
ifosfamide
change from N mustards to mustine
replacement of S with N-CH3
When are nitrogen mustards more cycotoxic? (cell cycle)
during replication phase of cell cycle
structure of nitrogen mustards
2 Cl on either side
N in middle
main target on DNA of nitrogen mustards/alkylating agents
N-7 of guanine
What does bi-functional mean?
they casue intRAstrand linking AND intERstrand linking
MOA of alkylating agents
MAIN MOA of alkylating agents
inter-strand cross linking
metabolism of alkylating agents
hydrolysis - most common
monoalkylation - also possible
Chlorambucil compared to other nitrogen mustards
AROMATIC RING replaces methyl group
- slowest acting
- least toxic
- less reactive than mustine
- only reacts with strong nucleophiles
- prevents some s/e