Differential expression of osteoblast-specific factor 2 and polymeric immunoglobulin receptor genes in nasopharyngeal carcinoma

Yao Chang, Tso Ching Lee, Jian Chiuan Li, Ting Lung Lai, Huey Huey Chua, Chi Long Chen, Shin Lian Doong, Chen Kung Chou, Tzung Shiahn Sheen, Ching Hwa Tsai

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Background. The molecular mechanisms leading to development of nasopharyngeal carcinoma (NPC) are not well understood. To delineate the features of NPC, we tried to identify unique expression of cellular genes in the tumor biopsy specimens. Methods and Results. By use of a combination of differential display and cDNA microarray analysis, we found two genes, 3E5 and 4A5, to show unique expression in the NPC biopsy specimens compared with nontumor nasopharyngeal tissues. Expression of 3E5, the osteoblast-specific factor-2 (OSF-2) gene, was detected at significantly higher levels in NPC biopsy specimens than that in control tissues, a finding confirmed using real-time quantitative reverse transcriptase-polymerase chain reaction (RT-PCR). A correlation between expression of OSF-2 and its regulatory cytokine transforming growth factor-β was observed in nontumor tissues but not in NPC biopsy specimens. On the other hand, expression of 4A5, whose sequences represent the 3′ untranslated region of the polymeric immunoglobulin receptor (pIgR) gene, was detected rarely in NPC specimens but frequently in nontumor controls. The expression of pIgR in normal epithelial cells, but not in NPC tumor cells, was verified by RT-PCR and immunohistochemical staining. Conclusions. NPC shows significant upregulation of OSF-2 and downregulation of pIgR. Expression of OSF-2 is likely to play a role in the pathogenesis of NPC. In addition, expression of OSF-2 and pIgR is disassociated with the expression of their regulatory cytokines in NPC biopsy specimens, suggesting that the tumors may have altered responses to certain cytokines.

Original languageEnglish
Pages (from-to)873-882
Number of pages10
JournalHead and Neck
Volume27
Issue number10
DOIs
Publication statusPublished - Oct 2005
Externally publishedYes

Fingerprint

Polymeric Immunoglobulin Receptors
Immunoglobulin Genes
Osteoblasts
Biopsy
Cytokines
Reverse Transcriptase Polymerase Chain Reaction
Nasopharyngeal carcinoma
Neoplasms
Transforming Growth Factors
3' Untranslated Regions
Microarray Analysis
Oligonucleotide Array Sequence Analysis
Genes
Up-Regulation
Down-Regulation

Keywords

  • Differential expression
  • Nasopharyngeal carcinoma
  • Osteoblast-specific factor-2
  • Polymeric immunoglobulin receptor
  • Transforming growth factor-β

ASJC Scopus subject areas

  • Otorhinolaryngology

Cite this

Differential expression of osteoblast-specific factor 2 and polymeric immunoglobulin receptor genes in nasopharyngeal carcinoma. / Chang, Yao; Lee, Tso Ching; Li, Jian Chiuan; Lai, Ting Lung; Chua, Huey Huey; Chen, Chi Long; Doong, Shin Lian; Chou, Chen Kung; Sheen, Tzung Shiahn; Tsai, Ching Hwa.

In: Head and Neck, Vol. 27, No. 10, 10.2005, p. 873-882.

Research output: Contribution to journalArticle

Chang, Y, Lee, TC, Li, JC, Lai, TL, Chua, HH, Chen, CL, Doong, SL, Chou, CK, Sheen, TS & Tsai, CH 2005, 'Differential expression of osteoblast-specific factor 2 and polymeric immunoglobulin receptor genes in nasopharyngeal carcinoma', Head and Neck, vol. 27, no. 10, pp. 873-882. https://doi.org/10.1002/hed.20253
Chang, Yao ; Lee, Tso Ching ; Li, Jian Chiuan ; Lai, Ting Lung ; Chua, Huey Huey ; Chen, Chi Long ; Doong, Shin Lian ; Chou, Chen Kung ; Sheen, Tzung Shiahn ; Tsai, Ching Hwa. / Differential expression of osteoblast-specific factor 2 and polymeric immunoglobulin receptor genes in nasopharyngeal carcinoma. In: Head and Neck. 2005 ; Vol. 27, No. 10. pp. 873-882.
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abstract = "Background. The molecular mechanisms leading to development of nasopharyngeal carcinoma (NPC) are not well understood. To delineate the features of NPC, we tried to identify unique expression of cellular genes in the tumor biopsy specimens. Methods and Results. By use of a combination of differential display and cDNA microarray analysis, we found two genes, 3E5 and 4A5, to show unique expression in the NPC biopsy specimens compared with nontumor nasopharyngeal tissues. Expression of 3E5, the osteoblast-specific factor-2 (OSF-2) gene, was detected at significantly higher levels in NPC biopsy specimens than that in control tissues, a finding confirmed using real-time quantitative reverse transcriptase-polymerase chain reaction (RT-PCR). A correlation between expression of OSF-2 and its regulatory cytokine transforming growth factor-β was observed in nontumor tissues but not in NPC biopsy specimens. On the other hand, expression of 4A5, whose sequences represent the 3′ untranslated region of the polymeric immunoglobulin receptor (pIgR) gene, was detected rarely in NPC specimens but frequently in nontumor controls. The expression of pIgR in normal epithelial cells, but not in NPC tumor cells, was verified by RT-PCR and immunohistochemical staining. Conclusions. NPC shows significant upregulation of OSF-2 and downregulation of pIgR. Expression of OSF-2 is likely to play a role in the pathogenesis of NPC. In addition, expression of OSF-2 and pIgR is disassociated with the expression of their regulatory cytokines in NPC biopsy specimens, suggesting that the tumors may have altered responses to certain cytokines.",
keywords = "Differential expression, Nasopharyngeal carcinoma, Osteoblast-specific factor-2, Polymeric immunoglobulin receptor, Transforming growth factor-β",
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AU - Chang, Yao

AU - Lee, Tso Ching

AU - Li, Jian Chiuan

AU - Lai, Ting Lung

AU - Chua, Huey Huey

AU - Chen, Chi Long

AU - Doong, Shin Lian

AU - Chou, Chen Kung

AU - Sheen, Tzung Shiahn

AU - Tsai, Ching Hwa

PY - 2005/10

Y1 - 2005/10

N2 - Background. The molecular mechanisms leading to development of nasopharyngeal carcinoma (NPC) are not well understood. To delineate the features of NPC, we tried to identify unique expression of cellular genes in the tumor biopsy specimens. Methods and Results. By use of a combination of differential display and cDNA microarray analysis, we found two genes, 3E5 and 4A5, to show unique expression in the NPC biopsy specimens compared with nontumor nasopharyngeal tissues. Expression of 3E5, the osteoblast-specific factor-2 (OSF-2) gene, was detected at significantly higher levels in NPC biopsy specimens than that in control tissues, a finding confirmed using real-time quantitative reverse transcriptase-polymerase chain reaction (RT-PCR). A correlation between expression of OSF-2 and its regulatory cytokine transforming growth factor-β was observed in nontumor tissues but not in NPC biopsy specimens. On the other hand, expression of 4A5, whose sequences represent the 3′ untranslated region of the polymeric immunoglobulin receptor (pIgR) gene, was detected rarely in NPC specimens but frequently in nontumor controls. The expression of pIgR in normal epithelial cells, but not in NPC tumor cells, was verified by RT-PCR and immunohistochemical staining. Conclusions. NPC shows significant upregulation of OSF-2 and downregulation of pIgR. Expression of OSF-2 is likely to play a role in the pathogenesis of NPC. In addition, expression of OSF-2 and pIgR is disassociated with the expression of their regulatory cytokines in NPC biopsy specimens, suggesting that the tumors may have altered responses to certain cytokines.

AB - Background. The molecular mechanisms leading to development of nasopharyngeal carcinoma (NPC) are not well understood. To delineate the features of NPC, we tried to identify unique expression of cellular genes in the tumor biopsy specimens. Methods and Results. By use of a combination of differential display and cDNA microarray analysis, we found two genes, 3E5 and 4A5, to show unique expression in the NPC biopsy specimens compared with nontumor nasopharyngeal tissues. Expression of 3E5, the osteoblast-specific factor-2 (OSF-2) gene, was detected at significantly higher levels in NPC biopsy specimens than that in control tissues, a finding confirmed using real-time quantitative reverse transcriptase-polymerase chain reaction (RT-PCR). A correlation between expression of OSF-2 and its regulatory cytokine transforming growth factor-β was observed in nontumor tissues but not in NPC biopsy specimens. On the other hand, expression of 4A5, whose sequences represent the 3′ untranslated region of the polymeric immunoglobulin receptor (pIgR) gene, was detected rarely in NPC specimens but frequently in nontumor controls. The expression of pIgR in normal epithelial cells, but not in NPC tumor cells, was verified by RT-PCR and immunohistochemical staining. Conclusions. NPC shows significant upregulation of OSF-2 and downregulation of pIgR. Expression of OSF-2 is likely to play a role in the pathogenesis of NPC. In addition, expression of OSF-2 and pIgR is disassociated with the expression of their regulatory cytokines in NPC biopsy specimens, suggesting that the tumors may have altered responses to certain cytokines.

KW - Differential expression

KW - Nasopharyngeal carcinoma

KW - Osteoblast-specific factor-2

KW - Polymeric immunoglobulin receptor

KW - Transforming growth factor-β

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