2006 Fiscal Year Final Research Report Summary
The relationship between single nucleotide polymorphism of matrix metallopraeinase-1 and metastasis of nasopharyngeal carcinoma.
| Project/Area Number |
16390487
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Otorhinolaryngology
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| Research Institution | Kanazawa University |
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Principal Investigator |
FURUKAWA Mitsuru Kanazawa University, Graduate School of Medical Science, Professor, 医学系研究科, 教授 (40092803)
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| Co-Investigator(Kenkyū-buntansha) |
YOSHIZAKI Tomokazu Kanazawa University, University Hospital, Assistant Professor, 医学部附属病院, 講師 (70262582)
MURONO Shigeyuki Kanazawa University, University Hospital, Assistant, 医学部附属病院, 助手 (20345622)
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| Project Period (FY) |
2004 – 2006
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| Keywords | NPC / EBV / SNP / LMP1 / MMP1 / Ets-1 |
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| Research Abstract |
The Epstein-Barr Virus (EBV) latent membrane protein 1 (LMP1) has a significant role in several malignancies, including nasopharyngeal carcinoma (NPC). LMP1 is principal onco-protein, and we have shown that it also induces a set of factors that mediated invasion, angiogenesis and metastasis. Matrix metarolloproteinase-1 (MMP1) is also involved in several malignancies. A single guanine insertion polymorphism (2G) in the MMP1 promoter creates an Ets binding site that causes high levels of transcription and correlates with risk for some malignancies. Here, we evaluate the impact of this 2G insertion type on NPC. We genotyped 44 Japanese and 39 Taiwanese NPC patients, as well as 58 Japanese and 23 Taiwanese healthy controls. The proportion of 2G homozybotes was higher in the NPC groups than controls (Japanese : p= 0.02, odds ratio (OR) =2.49 ; Taiwanese : p= 0.02, OR= 3.66). An analysis of overall survival rates in the patients with NPC, and the 1G/1G genotype disclosed a favorable prognosis (5-year survival rate = 100%, P= 0.04). Multivariate analysis showed that 1G/1G has independent prognostic significance. We also examined whether LMP1 enhances MMP1 expression in epithelial cells in culture. LMP1-transfected cells with 2G/2G genotype expressed MMP1, which was abolished by activator protein-1(AP1) dominant-negative (DN) and Ets-DN. LMP1 also induced active MMP3, which can cleave latent MMP1, and AP-1 DN-and Ets-DN suppressed the MMP3 expression. These results suggest that LMP1-induced MMP1 and MMP3 are closely linked and show that LMP1 activates MMP1 via an Ets binding site formed by 2G, which is a candidate marker for both risk and prognosis of NPC.
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