Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Naoyuki Homma"'
Autor:
Teiichiro Honda, Teiichi Motoyama, Satoshi Nishizuka, Gen Tamura, Kanji So, Naoyuki Homma, Naoyuki Togawa, Takayoshi Waki
Publikováno v:
Cancer Science. 97:1155-1158
A number of tumor suppressor and tumor-related genes are silenced by promoter hypermethylation in gastric cancer. Hypermethylation is not restricted to cancer cells, but is also present in non-neoplastic cells during aging. Such age-related methylati
Autor:
Gen Tamura, Teiichiro Honda, Teiichi Motoyama, Masanori Terashima, Makoto Endoh, Naoyuki Homma, Satoshi Nishizuka
Publikováno v:
British Journal of Cancer
RASSF2, a member of the RASSF1 family, has recently been identified as a potential tumour suppressor. We examined methylation status in multiple regions which included the CpG island and spanned the transcription start site of RASSF2 in 10 gastric ca
Autor:
Gen Tamura, Teiichiro Honda, Teiichi Motoyama, Naoyuki Homma, Satoshi Nishizuka, Makoto Endoh, Naoyuki Togawa, Kanji So
Publikováno v:
Pathology international. 56(10)
Silencing of the RUNX3 gene by hypermethylation of its promoter CpG island plays a major role in gastric carcinogenesis. To quantitatively evaluate RUNX3 methylation, a fiber-type DNA microarray was used on which methylated and unmethylated sequence
Autor:
Sumio Kawata, Teiichi Motoyama, Naoyuki Homma, Yutaka Matsumoto, Satoshi Nishizuka, Gen Tamura, Teiichiro Honda
Publikováno v:
Cancer science. 97(1)
RUNX3 is a novel tumor suppressor gene that is frequently silenced by promoter hypermethylation in gastric cancer. The methylation status of multiple regions within the RUNX3 promoter CpG island (3,478 bp) was examined in gastric cancer cell lines, p
Autor:
Sumio Kawata, Zhe Jin, Kiyonari Ohmura, Naoyuki Homma, Teiichi Motoyama, Teiichiro Honda, Gen Tamura
Publikováno v:
Virchows Archiv : an international journal of pathology. 446(2)
Human tumors are genetically unstable, and the instability exists at two distinct levels—the chromosomal level and the nucleotide level. Chfr and hMLH1 hypermethylation, which may lead to chromosomal instability (CIN) and microsatellite instability