Expression of multidrug resistance-associated proteins in rhabdomyosarcomas before and after chemotherapy
Autor: | E.J.S.M. de Bont, E. van den Berg, Rudy Komdeur, J.W. Klunder, W.M. Molenaar, Harald J. Hoekstra, W.T.A. van der Graaf |
---|---|
Přispěvatelé: | Damage and Repair in Cancer Development and Cancer Treatment (DARE), Stem Cell Aging Leukemia and Lymphoma (SALL) |
Jazyk: | angličtina |
Rok vydání: | 2003 |
Předmět: |
Adult
Male Pathology medicine.medical_specialty Adolescent multidrug resistance-associated proteins Cellular differentiation LINE ACUTE MYELOID-LEUKEMIA medicine.disease_cause TREATMENT LEADS THERAPEUTIC DIFFERENTIATION Pathology and Forensic Medicine Desmin CARCINOMA SW-620 CELLS medicine Humans ATP Binding Cassette Transporter Subfamily B Member 1 Rhabdomyosarcoma Child P-glycoprotein Vault Ribonucleoprotein Particles DRUG-RESISTANCE biology CHILDHOOD RHABDOMYOSARCOMAS Infant P-GLYCOPROTEIN Cell Differentiation differentiation medicine.disease GENE Neoplasm Proteins Multiple drug resistance lung resistance-related protein biology.protein ACTINOMYCIN-D Female lipids (amino acids peptides and proteins) Sarcoma Multidrug Resistance-Associated Protein 1 rhabdomyosarcoma Neoplasm Recurrence Local Carcinogenesis Multidrug Resistance-Associated Proteins |
Zdroj: | Human Pathology, 34(2), 150-155. W B SAUNDERS CO-ELSEVIER INC |
ISSN: | 0046-8177 |
Popis: | Rhabdomyosarcomas generally respond well to chemotherapy, and the residual lesions often are better differentiated than their primaries. This phenomenon may be explained by selective multidrug resistance (MDR) of differentiated tumor cell populations. We assess the role of MDR proteins in chemotherapy-induced differentiation in rhabdomyosarcomas in a clinical setting. Paraffin-embedded samples of 13 pairs of primary untreated rhabdomyosarcomas and their residual, recurrent, or metastatic lesions after chemotherapy were assessed for expression of MDR proteins, including P-glycoprotein (Pgp), multidrug resistance-associated protein (MRP-1), and lung resistance-related protein (LRP). Expression was semiquantitatively scored based on the percentage of isolated immunoreactive tumor cells as follows: 0, negative; 0.5, 75%. All specimens after chemotherapy, except the late recurrences, were better differentiated than their primary, untreated specimens. Pgp or MRP-1 expression did not change significantly, but LRP expression increased significantly after chemotherapy. In both untreated and treated samples, LRP was expressed primarily in differentiated cells. The findings indicate that the in vivo expression of LRP, but not of Pgp and MRP-1, is induced by chemotherapeutic treatment in rhabdomyosarcomas. The preferential expression of LRP in differentiated cells and the subsequent more extensive expression after chemotherapy suggests that LRP plays a role in therapy-induced differentiation. Copyright 2003, Elsevier Science (USA). All rights reserved. |
Databáze: | OpenAIRE |
Externí odkaz: |