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EXPRESSION OF ABC TRANSPORTERS AND CHANGES IN LYMPHOCYTE SUBPOPULATIONS
IN RESPONSE TO HYPERTHERMIC LIMB PERFUSION
Peter Hohenberger, MD (Robert-Roessle Hospital, Charité, Berlin,
Germany)
Problem and approach: Multidrug resistance genes interfere with response
to sarcoma chemotherapy. Hyperthermic limb perfusion (ILP) yields up to 30%
pCRs. The contributing factors remain unclear: drug concentration, application
of hyperthermia, stimulation of T-lymphocytes? We evaluated
- the involvement of ABC transporters (MDR1/PGP and MRP1) and
- leucocyte subpopulations prior, during, and after ILP
Methods: Snap-frozen tumor biopsies obtained prior and after 1LP were
used to analyze the expression of MRP1 and MDR1/PGP on the mRNA level by quantitative
real time RT-PCR after micro-dissection and at the protein level by ICH with
antibodies MRK16 + C219 for PGP and MRPr1 + MRPm6 for MRP1. Sera were collected
prior and 24h after ILP and from the perfusate and examined for CD3, CD4, CD8,
CD20, CD45, CD56, CD68 + cells. Materials from 19 pts. were analyzed undergoing
ILP with rhTNFa + melphalan, or melphalan+CDDP+/- adriamycin.
Results: An increase of MDR1/PGP as well as MRP gene expression could
be detected, but maximum and duration of MDR1 or MRP induction varied between
patients and drugs used. No clear influence of histological typing or the expression
prior to ILP could be found. A significant rise in leuco- and a drop in lymphocytes
after ILP could be observed. CD4:CD8 ratio remained unchanged, as well as B-cell
and NK-cell count. Within the perfusate, monocytes completely disappeared.
Conclusion: Response to ILP is not uniform. The induction of MDR1/PGP
and MRP by hyperthermia may interfere with the advantage of increased drug dosages.
T-cell mediated tumor regression seems not to play a major role. Influencing
factors such as hyperthermia and vascularity must be determined. Further analysis
of the factors is important to select the right drugs applied in an optimized
sequence.
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