2006 Fiscal Year Final Research Report Summary
Study on patho-epidemiology of malignant lymphoma in Japan
| Project/Area Number |
16390105
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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 |
Human pathology
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| Research Institution | Osaka University |
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Principal Investigator |
AOZASA Katsuyuki Osaka University, Graduate School of Medicine, professor, 医学系研究科, 教授 (30115985)
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| Co-Investigator(Kenkyū-buntansha) |
TOMITA Yasuhiko Osaka University, Graduate School of Medicine, Associate professor, 医学系研究科, 助教授 (60263266)
TAKAKUWA Tetsuya Osaka University, Graduate School of Medicine, Associate professor, 医学系研究科, 助教授 (40244933)
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| Project Period (FY) |
2004 – 2006
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| Keywords | malignant lymphoma / etiology / EB virus / rheumatoid arthritis / prognosis |
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| Research Abstract |
The study based on the cases with malignant lymphomas registered in the Osaka Lymphoma Study Group and the cases with pyothorax-associated lymphoma (PAL) and nasal NK/T-cell lymphoma (NKTCL). Malignant lymphomas developed in rheumatoid arthritis were also included. Epidemiological and molecular analysis were performed on these cases. The main findings obtained from these findings were as follows.
1. Case-control study in Japan(5 institutes), Korea (Yonsei Univ), and China (China Medical Univ) revealed that pesticides and chemical solvents were risk factors for development of NKTCL (Int J Cancer 2006).
2. PAL is an EBV-associated lymphoma. Loss of EBNA-2 one of EBV-coded latent genes, correlated with prognosis of PAL patients (Int J Cancer 2006).
3. It is known that lymphoproliferative disease (LPD) develop relative frequently in patients with rheumatoid arthritis (RA), in which methotrexate (MTX) administration for RA is supposed to be involved. Then we compared the RA-LPD with and without MT X medication, showing no fundamental differences between them. (J Rheum 2007).
4.Mutations of DNA mismatch repair genes, ATM, ATR, and MRE 11, in 50 cell lines from lymphoid leukemias and lymphomas, were examined. Mutations of ATM and MRE 11 were occasionally found. These mutations might cause genome instability, and finally result in lymphoid neoplasias. (Cancer Sci 2006).
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