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Genetic alterations of HLA‐class II in ovarian cancer
Author(s) -
Kübler Kirsten,
Arndt Peter F.,
Wardelmann Eva,
Landwehr Christina,
Krebs Dieter,
Kuhn Walther,
van der Ven Katrin
Publication year - 2008
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.23624
Subject(s) - biology , human leukocyte antigen , ovarian cancer , immune system , major histocompatibility complex , phenotype , cancer , allele , immunology , ovarian carcinoma , antigen , cancer research , oncogene , genetics , gene , cell cycle
Abstract The immune system controls tumor formation through identification and elimination of cellular alterations. Consequently, cancer development in immune competent hosts depends on strategies to evade the immune system. Modulation of tumor antigen‐specific immune responses by aberrant expression of HLA‐class I and II molecules is well documented in a variety of carcinomas including ovarian cancer. To date, little data are available about molecular mechanisms responsible for altered HLA‐class II phenotypes in tumors. In our sample of 10 Caucasian patients with ovarian carcinoma, a semiquantitative analysis was performed for HLA‐class II loci DRB1 and DQB1 in malignant and normal ovarian tissue. Gene amplifications were identified in 62.5% of analyzed alleles and deletions in 17.5%, demonstrating that genomic aberrations of 6p21.3 are common and that copy number gain is more frequent than loss. Moreover, amplifications are most pronounced in advanced‐stage tumors. To evaluate genotype‐phenotype relation, immunohistochemical analyses were performed and revealed de novo expression of HLA‐class II in 30% of tumors with an inverse association between antigen level and HLA copy number. It remains to be elucidated whether the profound changes of the latter quantities are the result of the host's immunological self‐defense, indicate the presence of an oncogene located within the MHC‐complex or merely reflect the increasing loss of differentiation of the tumor tissue. © 2008 Wiley‐Liss, Inc.