Identification of signals involved melanomagenesis and melanoma growth, expecially, UV-induced melanoma formation
Project/Area Number |
22591221
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Dermatology
|
Research Institution | Nippon Medical School |
Principal Investigator |
FUNASAKA Yoko 日本医科大学, 医学部, 准教授 (30209150)
|
Project Period (FY) |
2010 – 2012
|
Project Status |
Completed (Fiscal Year 2012)
|
Budget Amount *help |
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2012: ¥390,000 (Direct Cost: ¥300,000、Indirect Cost: ¥90,000)
Fiscal Year 2011: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2010: ¥2,860,000 (Direct Cost: ¥2,200,000、Indirect Cost: ¥660,000)
|
Keywords | 悪性黒色腫 / 発癌 / メラニン / 紫外線 / DNA 損傷 / DNA損傷 / シグナル |
Research Abstract |
Fair skin caucasians with red hair are more susceptible to UV-induced melanoma. We generated melanoma model mouse harboring epidermal melanocytes with different melanin species, then irradiated with UVB or UVA. UVA irradiation did not accelerate melanoma formation, however, UVB did so. Especially, pheomlanin, which is produced more in caucasians. Pheomelanin containing epidermis showed prolonged CPDs after UVB irradiation. DNA repair-deficient mouse also showed early melanoma formation. These results indicate that DNA damages caused by UVB and pheomelanin could be a trigger of melanoma formation.
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Report
(4 results)
Research Products
(14 results)