PMID- 10519360 OWN - NLM STAT- MEDLINE DCOM- 20000225 LR - 20220317 IS - 0001-2815 (Print) IS - 0001-2815 (Linking) VI - 54 IP - 3 DP - 1999 Sep TI - HLA class I expression and chromosomal deletions at 6p and 15q in head and neck squamous cell carcinomas. PG - 235-45 AB - Loss at the chromosomal region 6p21.3 is a frequent event in head and neck squamous cell carcinomas (HNSCC). Since the human leukocyte antigen (HLA) complex is located at 6p21.3, loss of heterozygosity (LOH) of this region may provide tumour cells with an immune-escape tumour phenotype. In the present study, we have studied the correlation of HLA class I, TAP1 and TAP2 expression and LOH at 6p21.3. HLA class I and TAP1 and TAP2 protein expression was analysed by immunohistochemical procedures. A panel of 41 HNSCC with downregulated HLA class I expression was selected for LOH studies using 5 microsatellite markers located at 6p21.3 (D6S105, D6S265, D6S276, D6S273, D6S291) and 2 markers located at the chromosome 6 centromere (D6S473) and the 6p telomere (D6S277). In addition, LOH of the beta-2-nmicroglobulin (beta2m) gene was studied using 2 microsatellite markers flanking the beta2m gene (D15S126 and D15S153) and was correlated with beta2m and HLA class I expression. In 20/41 (49%) of the HNSCC, allelic loss for at least one locus at 6p21.3 was found. Loss at 15q was found in 4/10 (40%) HNSCC with downregulated beta2m expression and in 12/41 (29%) HNSCC with downregulated HLA class I expression. Our data show that downregulation of HLA class I expression is correlated with loss of chromosomal regions at 6p21.3 in HNSCC. In addition, LOH at 6p21.3 and 15q in 10 paired samples of DNA derived from the primary HNSCC, the lymph node metastases and from peripheral blood lymphocytes (PBLs) was studied. Five (5/10) primary tumours contained the same deletion as the corresponding lymph node metastases. The other cases contained deletions either in the primary tumour (3 cases) or in the lymph node metastases (1 case) or no deletions at all (1 case). FAU - Feenstra, M AU - Feenstra M AD - Department of Pathology, University Hospital, Utrecht, The Netherlands. FAU - Veltkamp, M AU - Veltkamp M FAU - van Kuik, J AU - van Kuik J FAU - Wiertsema, S AU - Wiertsema S FAU - Slootweg, P AU - Slootweg P FAU - van den Tweel, J AU - van den Tweel J FAU - de Weger, R AU - de Weger R FAU - Tilanus, M AU - Tilanus M LA - eng PT - Journal Article PL - England TA - Tissue Antigens JT - Tissue antigens JID - 0331072 RN - 0 (ATP Binding Cassette Transporter, Subfamily B, Member 2) RN - 0 (ATP Binding Cassette Transporter, Subfamily B, Member 3) RN - 0 (ATP-Binding Cassette Transporters) RN - 0 (DNA, Neoplasm) RN - 0 (HLA Antigens) RN - 0 (HLA-A Antigens) RN - 0 (Histocompatibility Antigens Class I) RN - 0 (TAP1 protein, human) RN - 0 (beta 2-Microglobulin) RN - 145892-13-3 (TAP2 protein, human) SB - IM MH - ATP Binding Cassette Transporter, Subfamily B, Member 2 MH - ATP Binding Cassette Transporter, Subfamily B, Member 3 MH - ATP-Binding Cassette Transporters/genetics MH - Carcinoma, Squamous Cell/chemistry/*genetics MH - *Chromosome Deletion MH - Chromosome Mapping MH - *Chromosomes, Human, Pair 15 MH - *Chromosomes, Human, Pair 6 MH - Cytoplasm/chemistry MH - DNA, Neoplasm MH - HLA Antigens/*biosynthesis MH - HLA-A Antigens/biosynthesis/genetics MH - Head and Neck Neoplasms/chemistry/*genetics MH - Histocompatibility Antigens Class I/*biosynthesis MH - Humans MH - Immunohistochemistry MH - Loss of Heterozygosity/genetics MH - Lymph Nodes MH - Lymphatic Metastasis MH - Major Histocompatibility Complex MH - Microsatellite Repeats MH - Trinucleotide Repeat Expansion MH - beta 2-Microglobulin/genetics EDAT- 1999/10/16 09:00 MHDA- 2000/03/04 09:00 CRDT- 1999/10/16 09:00 PHST- 1999/10/16 09:00 [pubmed] PHST- 2000/03/04 09:00 [medline] PHST- 1999/10/16 09:00 [entrez] AID - 10.1034/j.1399-0039.1999.540304.x [doi] PST - ppublish SO - Tissue Antigens. 1999 Sep;54(3):235-45. doi: 10.1034/j.1399-0039.1999.540304.x.