Immune dysregulation and tumor-associated gene changes in recurrent respiratory papillomatosis: a paired microarray analysis

• Published in: Molecular medicine (Cambridge, Mass.) Mass.), 2008-09, Vol.14 (9-10), p.608-617
• Main Authors: DeVoti, James A, Rosenthal, David W, Wu, Rong, Abramson, Allan L, Steinberg, Bettie M, Bonagura, Vincent R
• Format: Article
• Language: English
• Subjects: Gene Expression Profiling; Gene Expression Regulation; Human papillomavirus 11 - immunology; Human papillomavirus 11 - pathogenicity; Human papillomavirus 6 - immunology; Human papillomavirus 6 - pathogenicity; Humans; Laryngeal Mucosa - immunology; Laryngeal Mucosa - metabolism; Laryngeal Mucosa - pathology; Laryngeal Neoplasms - genetics; Laryngeal Neoplasms - immunology; Laryngeal Neoplasms - physiopathology; Laryngeal Neoplasms - virology; Larynx - cytology; Larynx - immunology; Larynx - pathology; Larynx - virology; Oligonucleotide Array Sequence Analysis - methods; Papilloma - genetics; Papilloma - immunology; Papilloma - physiopathology; Papilloma - virology; Proteins - genetics; Proteins - metabolism; Recurrence; Severity of Illness Index
• ISSN: 1076-1551; 1528-3658
• DOI: 10.2119/2008-00060.DeVoti

Recurrent respiratory papillomas (RRP) are benign airway tumors, caused primarily by human papillomaviruses (HPV) types 6 and 11. The disease is characterized by multiple recurrences after surgical removal, with limited effective therapy. To identify novel targets for future therapy, we established transcriptional profiles for actively growing papillomas compared with autologous, clinically normal, laryngeal epithelia (adjacent tissue). Total ribonucleic acid (RNA) from 12 papillomas and 12 adjacent tissues were analyzed by microarray, and the matched sets of tissues compared by paired t test, to identify differentially expressed genes in papilloma tissues while minimizing variations intrinsic to individual patients. Quantitative polymerase chain reaction (PCR) was used to confirm the relative expression levels for a subset of genes. Within the 109 differentially expressed transcripts whose expression varied at least three-fold were two large groups of genes with related functions. The first group consisted of 18 genes related to host defense, including both innate and adaptive immunity. The second group contained 37 genes that likely contribute to growth of papillomas as benign tumors, since the altered pattern of expression also had been reported previously in many cancers. Our results support our previous studies that document a systemic T(H)2-like adaptive immune response in RRP, and suggest that there is a role for altered innate immunity in RRP as well. We propose that HPV 6 and 11 infection establishes a tumorigenic microenvironment characterized by alteration of both innate inflammatory signals and adaptive immune responses that prevent effective T(H)1-like response, in conjunction with altered expression of numerous genes that regulate cellular growth and differentiation.