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   <subfield code="a">Interstitial fluid pressure is increased in renal cell carcinoma xenografts</subfield>
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   <subfield code="c">[Detlef Rohde, Christoph Wiesner, Dirk Graf, Johannes Wolff, Laszlo Füzesi, Gerhard Jakse]</subfield>
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   <subfield code="a">The purpose of this study was to test the hypothesis that renal cell carcinoma (RCC) exhibits an increased intratumoral interstitial fluid pressure (IT-IFP). Therefore, resected tumors from human primary (n = 23) or metastatic RCC (n = 3) were xenografted in SCID mice. The IFP of single tumor nodules (n = 65) and normal mouse tissue (n = 195) was measured by means of the &quot;wick-in-needle” technique. Data demonstrate that the mean IT-IFP at neoplasia was 35 times greater than in normal tissue, and decreased precipitously at the tumor boundary. IT-IFP values tended to increase with the grade of malignancy of the tumor cells and tumor size. The mean IT-IFP of xenografts derived from primary RCC was twice as high as that from metastatic RCC tissue. These findings indicate a biophysical barrier to drug delivery in RCC; this may, in concert with cellular-based drug resistance mechanisms, be an additional explanation for resistance of the tumor to certain blood-borne anticancer therapies.</subfield>
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   <subfield code="a">Key words Drug delivery system</subfield>
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   <subfield code="a">Neoplasm, metastasis, physiopathology</subfield>
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