An analysis of cell lineage for breast cancer by gene alteration of mitochondria DNA D-loop region
Project/Area Number |
24590433
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Human pathology
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Research Institution | Nihon University |
Principal Investigator |
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Co-Investigator(Renkei-kenkyūsha) |
ESUMI Mariko 日本大学, 医学部, 准教授 (10147019)
TOU Shoen 日本大学, 医学部, 助教 (20326036)
FUCHINOUE Fumi 日本大学, 医学部, 助手 (10409021)
AMANO Sadao 日本大学, 医学部, 准教授 (80159459)
SAKURAI Kenichi 日本大学, 医学部, 講師 (20366602)
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Project Period (FY) |
2012-04-01 – 2015-03-31
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Project Status |
Completed (Fiscal Year 2014)
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Budget Amount *help |
¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2014: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2013: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2012: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
|
Keywords | 乳癌 / 遺伝子変異多様性 / クロナリティ / ミトコンドリアDNA D-loop領域 / ミトコンドリアDNA / 癌細胞系譜 / クロナリティー / 細胞系譜 / 再発 |
Outline of Final Research Achievements |
(1)Gene alteration of mtDNA-DL (GAMDDL) was detected in metachronously resected ipsilateral normal breast (0.03%)and contralateral breast (0.74%).(2)Breast cancers with polysomy of centromere 17 and those with HER2 gene heterogeneity were not overlapped. (3)The protocol to visualize HER2 protein and gene simultaneously was established.(4)Primary breast cancer with heterogeneity, e.g. with and without HER2 gene amplification, and recurrent tumor without HER2 gene amplification was analyzed by GAMDDL method. There are differences of MDDL between carcinoma cells of primary tumor with and without HER2 gene amplification.
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Report
(4 results)
Research Products
(11 results)
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[Journal Article] Altered intracellular region of MUC1 and disrupted correlation of polarity-related molecules in breast cancer subtypes.2015
Author(s)
Iizuka M, Nakanishi Y, Fuchinoue F, Maeda T, Murakami E, Obana Y, Enomoto K, Tani M, Sakurai K, Amano S, Masuda S.
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Journal Title
Cancer Science
Volume: 106
Issue: 3
Pages: 307-314
DOI
Related Report
Peer Reviewed / Open Access
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[Journal Article] Overexpression of PGC1α and accumulation of p62 in apocrine carcinoma of the breast.2015
Author(s)
Fuchinoue F, Hirotani Y, Nakanishi Y, Yamaguchi H, Nishimaki H, Noda H, Tang X, Iiuzuka M, Amano S, Sugitani M, Nemoto N, Masuda S.
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Journal Title
Patholology International
Volume: 65
Issue: 1
Pages: 19-26
DOI
Related Report
Peer Reviewed
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[Journal Article] The cell cycle profiling-risk score based on CDK1 and 2 predicts early recurrence in node-negative, hormone receptor-positive breast cancer treated with endocrine therapy.2014
Author(s)
Kim SJ, Masuda N, Tsukamoto F, Inaji H, Akiyama F, Sonoo H, Kurebayashi J, Yoshidome K, Tsujimoto M, Takei H, Masuda S, Nakamura S, Noguchi S.
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Journal Title
Cancer Lett.
Volume: 355
Issue: 2
Pages: 217-223
DOI
Related Report
Peer Reviewed / Open Access
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[Journal Article] Prognostic Significance of the Ki67 Scoring Categories in Breast Cancer Subgroups.2014
Author(s)
Niikura N, Masuda S, Kumaki N, Tang X, Terada M, Terao M, Iwamoto T, Oshitanai R, Morioka T, Tuda B, Okamura T, Saito Y, Suzuki Y, Tokuda Y.
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Journal Title
Clinical Breast Cancer
Volume: 14
Issue: 5
Pages: 323-329
DOI
Related Report
Peer Reviewed
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[Journal Article] Immunohistochemical Ki67 labeling index has a similar proliferation predictive power as various gene signatures in breast cancer.2012
Author(s)
Niikura N, Iwamoto T, Masuda S, Kumaki N, Tang X, Shirane M, Mori K, Tsuda B, Okamura T, Saito Y, Suzuki Y, Tokuda Y.
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Journal Title
Cancer Sci
Volume: 103
Issue: 8
Pages: 1508-12
DOI
Related Report
Peer Reviewed