Effect of modulation of the transferrin receptor on gallium-67 uptake and cytotoxicity in lymphoma cell lines

• Published in: British journal of cancer 1996-08, Vol.74 (4), p.619-624
• Main Authors: van Leeuwen-Stok, AE, Schuurhuis, GJ, Dräger, AM, Visser-Platier, AWJ, Teule, GJJ, Huijgens, PC
• Format: Article
• Language: English
• Subjects: Antineoplastic agents; Antineoplastic Agents - toxicity; Biological and medical sciences; Biological Transport; Biomedical and Life Sciences; Biomedicine; Cancer Research; Cell Cycle - drug effects; Cell Division - drug effects; Cell Line; Cell Survival - drug effects; Cell Survival - radiation effects; Cytarabine - toxicity; Drug Resistance; Epidemiology; experimental-oncology; Flow Cytometry; Gallium Radioisotopes - pharmacokinetics; Gallium Radioisotopes - toxicity; Gene Expression - drug effects; General aspects; Humans; Hydroxyurea - toxicity; Lymphoma; Medical sciences; Methotrexate - toxicity; Molecular Medicine; Oncology; Pharmacology. Drug treatments; Receptors, Transferrin - biosynthesis; Tumor Cells, Cultured; Tumor Stem Cell Assay
• ISSN: 0007-0920; 1532-1827
• DOI: 10.1038/bjc.1996.411

Gallium-67 is a radionuclide that accumulates in haematological malignancies and is used for diagnostic purposes. Uptake of 67Ga into the cell occurs via the transferrin receptor, which is differentially expressed during the various cell cycle phases. With the aim of selectively increasing 67Ga uptake, we studied whether the transferrin receptor (TfR) expression could be modulated in the U937 and U715 lymphoma cell lines by cytostatic drugs inducing cell cycle phase accumulation. We tested clinically relevant drugs such as 1-beta-D-arabinofuranosylcytosine (Ara-C), hydroxyurea and methotrexate. Cytotoxicity was determined by testing the clonogenic capacity of the lymphoma cell lines. All three drugs induced an increase in S-phase content, TfR expression and 67Ga uptake in U937 and U715 single cells. The combinations of drugs and 67Ga resulted in an additive effect on the clonogenic capacity. In U937 spheroids, cultured by the fibrin clot technique, we found an accumulation in the S-phase too as well as an increase of the transferrin receptor expression after Ara-C preincubation. As in single cells 67Ga uptake was increased without synergistic effects on the clonogenic capacity. In conclusion, priming with drugs induces increased transferrin receptor expression and 67Ga uptake. Inhibition of clonogenic capacity was additive rather than synergistic.