Ectopic Expression

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Masae Tatematsu - One of the best experts on this subject based on the ideXlab platform.

  • down regulation of a gastric transcription factor sox2 and Ectopic Expression of intestinal homeobox genes cdx1 and cdx2 inverse correlation during progression from gastric intestinal mixed to complete intestinal metaplasia
    Journal of Cancer Research and Clinical Oncology, 2004
    Co-Authors: Tetsuya Tsukamoto, Ken Ichi Inada, Harunari Tanaka, Tsutomu Mizoshita, Mami Mihara, Toshikazu Ushijima, Yoshitaka Yamamura, Shigeo Nakamura, Masae Tatematsu
    Abstract:

    Purpose The molecular mechanisms underlying the development of intestinal metaplasia (IM) of the human stomach have yet to be clarified in detail. Besides Ectopic Expression of intestinal transcription factors, Cdx1 and Cdx2, little information is available regarding other regulatory factors. Hence, we here analyzed Sox2, a human homolog of a chicken gastric transcription factor, with reference to our new classification for gastric/intestinal (GI)-mixed type IM.

  • down regulation of a gastric transcription factor sox2 and Ectopic Expression of intestinal homeobox genes cdx1 and cdx2 inverse correlation during progression from gastric intestinal mixed to complete intestinal metaplasia
    Journal of Cancer Research and Clinical Oncology, 2004
    Co-Authors: Tetsuya Tsukamoto, Ken Ichi Inada, Harunari Tanaka, Tsutomu Mizoshita, Mami Mihara, Toshikazu Ushijima, Yoshitaka Yamamura, Shigeo Nakamura, Masae Tatematsu
    Abstract:

    The molecular mechanisms underlying the development of intestinal metaplasia (IM) of the human stomach have yet to be clarified in detail. Besides Ectopic Expression of intestinal transcription factors, Cdx1 and Cdx2, little information is available regarding other regulatory factors. Hence, we here analyzed Sox2, a human homolog of a chicken gastric transcription factor, with reference to our new classification for gastric/intestinal (GI)-mixed type IM. Twenty specimens of surgically resected antral mucosa were subjected to a gland isolation technique. Isolated glands were classified into gastric (G), GI-mixed, and solely intestinal (I) types according to Alcian blue and paradoxical concanavalin A staining and were quantified for mRNA levels of gastrointestinal markers. MUC5AC and MUC6 transcripts decreased with the progression of IM, while MUC2 and villin-1 were inversely correlated. Sox2 showed a gradual decrease from G, through GI, to the I type (G vs GI and GI vs I, P<0.01 and P<0.005, respectively). On the other hand, Cdx1 (G vs GI and GI vs I, P<0.0001 and P=0.337, respectively) and Cdx2 (G vs GI and GI vs I, P<0.0001 and P<0.05, respectively) appeared in IM. Immunohistochemical study confirmed decreased Expression of Sox2 and Ectopic emergence of Cdx2 protein in IM glands. Down-regulation of Sox2, besides Ectopic Expression of Cdx genes, may be important factors for the development of IM.

Tetsuya Tsukamoto - One of the best experts on this subject based on the ideXlab platform.

  • down regulation of a gastric transcription factor sox2 and Ectopic Expression of intestinal homeobox genes cdx1 and cdx2 inverse correlation during progression from gastric intestinal mixed to complete intestinal metaplasia
    Journal of Cancer Research and Clinical Oncology, 2004
    Co-Authors: Tetsuya Tsukamoto, Ken Ichi Inada, Harunari Tanaka, Tsutomu Mizoshita, Mami Mihara, Toshikazu Ushijima, Yoshitaka Yamamura, Shigeo Nakamura, Masae Tatematsu
    Abstract:

    Purpose The molecular mechanisms underlying the development of intestinal metaplasia (IM) of the human stomach have yet to be clarified in detail. Besides Ectopic Expression of intestinal transcription factors, Cdx1 and Cdx2, little information is available regarding other regulatory factors. Hence, we here analyzed Sox2, a human homolog of a chicken gastric transcription factor, with reference to our new classification for gastric/intestinal (GI)-mixed type IM.

  • down regulation of a gastric transcription factor sox2 and Ectopic Expression of intestinal homeobox genes cdx1 and cdx2 inverse correlation during progression from gastric intestinal mixed to complete intestinal metaplasia
    Journal of Cancer Research and Clinical Oncology, 2004
    Co-Authors: Tetsuya Tsukamoto, Ken Ichi Inada, Harunari Tanaka, Tsutomu Mizoshita, Mami Mihara, Toshikazu Ushijima, Yoshitaka Yamamura, Shigeo Nakamura, Masae Tatematsu
    Abstract:

    The molecular mechanisms underlying the development of intestinal metaplasia (IM) of the human stomach have yet to be clarified in detail. Besides Ectopic Expression of intestinal transcription factors, Cdx1 and Cdx2, little information is available regarding other regulatory factors. Hence, we here analyzed Sox2, a human homolog of a chicken gastric transcription factor, with reference to our new classification for gastric/intestinal (GI)-mixed type IM. Twenty specimens of surgically resected antral mucosa were subjected to a gland isolation technique. Isolated glands were classified into gastric (G), GI-mixed, and solely intestinal (I) types according to Alcian blue and paradoxical concanavalin A staining and were quantified for mRNA levels of gastrointestinal markers. MUC5AC and MUC6 transcripts decreased with the progression of IM, while MUC2 and villin-1 were inversely correlated. Sox2 showed a gradual decrease from G, through GI, to the I type (G vs GI and GI vs I, P<0.01 and P<0.005, respectively). On the other hand, Cdx1 (G vs GI and GI vs I, P<0.0001 and P=0.337, respectively) and Cdx2 (G vs GI and GI vs I, P<0.0001 and P<0.05, respectively) appeared in IM. Immunohistochemical study confirmed decreased Expression of Sox2 and Ectopic emergence of Cdx2 protein in IM glands. Down-regulation of Sox2, besides Ectopic Expression of Cdx genes, may be important factors for the development of IM.

Yoshitaka Yamamura - One of the best experts on this subject based on the ideXlab platform.

  • down regulation of a gastric transcription factor sox2 and Ectopic Expression of intestinal homeobox genes cdx1 and cdx2 inverse correlation during progression from gastric intestinal mixed to complete intestinal metaplasia
    Journal of Cancer Research and Clinical Oncology, 2004
    Co-Authors: Tetsuya Tsukamoto, Ken Ichi Inada, Harunari Tanaka, Tsutomu Mizoshita, Mami Mihara, Toshikazu Ushijima, Yoshitaka Yamamura, Shigeo Nakamura, Masae Tatematsu
    Abstract:

    Purpose The molecular mechanisms underlying the development of intestinal metaplasia (IM) of the human stomach have yet to be clarified in detail. Besides Ectopic Expression of intestinal transcription factors, Cdx1 and Cdx2, little information is available regarding other regulatory factors. Hence, we here analyzed Sox2, a human homolog of a chicken gastric transcription factor, with reference to our new classification for gastric/intestinal (GI)-mixed type IM.

  • down regulation of a gastric transcription factor sox2 and Ectopic Expression of intestinal homeobox genes cdx1 and cdx2 inverse correlation during progression from gastric intestinal mixed to complete intestinal metaplasia
    Journal of Cancer Research and Clinical Oncology, 2004
    Co-Authors: Tetsuya Tsukamoto, Ken Ichi Inada, Harunari Tanaka, Tsutomu Mizoshita, Mami Mihara, Toshikazu Ushijima, Yoshitaka Yamamura, Shigeo Nakamura, Masae Tatematsu
    Abstract:

    The molecular mechanisms underlying the development of intestinal metaplasia (IM) of the human stomach have yet to be clarified in detail. Besides Ectopic Expression of intestinal transcription factors, Cdx1 and Cdx2, little information is available regarding other regulatory factors. Hence, we here analyzed Sox2, a human homolog of a chicken gastric transcription factor, with reference to our new classification for gastric/intestinal (GI)-mixed type IM. Twenty specimens of surgically resected antral mucosa were subjected to a gland isolation technique. Isolated glands were classified into gastric (G), GI-mixed, and solely intestinal (I) types according to Alcian blue and paradoxical concanavalin A staining and were quantified for mRNA levels of gastrointestinal markers. MUC5AC and MUC6 transcripts decreased with the progression of IM, while MUC2 and villin-1 were inversely correlated. Sox2 showed a gradual decrease from G, through GI, to the I type (G vs GI and GI vs I, P<0.01 and P<0.005, respectively). On the other hand, Cdx1 (G vs GI and GI vs I, P<0.0001 and P=0.337, respectively) and Cdx2 (G vs GI and GI vs I, P<0.0001 and P<0.05, respectively) appeared in IM. Immunohistochemical study confirmed decreased Expression of Sox2 and Ectopic emergence of Cdx2 protein in IM glands. Down-regulation of Sox2, besides Ectopic Expression of Cdx genes, may be important factors for the development of IM.

Shigeo Nakamura - One of the best experts on this subject based on the ideXlab platform.

  • down regulation of a gastric transcription factor sox2 and Ectopic Expression of intestinal homeobox genes cdx1 and cdx2 inverse correlation during progression from gastric intestinal mixed to complete intestinal metaplasia
    Journal of Cancer Research and Clinical Oncology, 2004
    Co-Authors: Tetsuya Tsukamoto, Ken Ichi Inada, Harunari Tanaka, Tsutomu Mizoshita, Mami Mihara, Toshikazu Ushijima, Yoshitaka Yamamura, Shigeo Nakamura, Masae Tatematsu
    Abstract:

    Purpose The molecular mechanisms underlying the development of intestinal metaplasia (IM) of the human stomach have yet to be clarified in detail. Besides Ectopic Expression of intestinal transcription factors, Cdx1 and Cdx2, little information is available regarding other regulatory factors. Hence, we here analyzed Sox2, a human homolog of a chicken gastric transcription factor, with reference to our new classification for gastric/intestinal (GI)-mixed type IM.

  • down regulation of a gastric transcription factor sox2 and Ectopic Expression of intestinal homeobox genes cdx1 and cdx2 inverse correlation during progression from gastric intestinal mixed to complete intestinal metaplasia
    Journal of Cancer Research and Clinical Oncology, 2004
    Co-Authors: Tetsuya Tsukamoto, Ken Ichi Inada, Harunari Tanaka, Tsutomu Mizoshita, Mami Mihara, Toshikazu Ushijima, Yoshitaka Yamamura, Shigeo Nakamura, Masae Tatematsu
    Abstract:

    The molecular mechanisms underlying the development of intestinal metaplasia (IM) of the human stomach have yet to be clarified in detail. Besides Ectopic Expression of intestinal transcription factors, Cdx1 and Cdx2, little information is available regarding other regulatory factors. Hence, we here analyzed Sox2, a human homolog of a chicken gastric transcription factor, with reference to our new classification for gastric/intestinal (GI)-mixed type IM. Twenty specimens of surgically resected antral mucosa were subjected to a gland isolation technique. Isolated glands were classified into gastric (G), GI-mixed, and solely intestinal (I) types according to Alcian blue and paradoxical concanavalin A staining and were quantified for mRNA levels of gastrointestinal markers. MUC5AC and MUC6 transcripts decreased with the progression of IM, while MUC2 and villin-1 were inversely correlated. Sox2 showed a gradual decrease from G, through GI, to the I type (G vs GI and GI vs I, P<0.01 and P<0.005, respectively). On the other hand, Cdx1 (G vs GI and GI vs I, P<0.0001 and P=0.337, respectively) and Cdx2 (G vs GI and GI vs I, P<0.0001 and P<0.05, respectively) appeared in IM. Immunohistochemical study confirmed decreased Expression of Sox2 and Ectopic emergence of Cdx2 protein in IM glands. Down-regulation of Sox2, besides Ectopic Expression of Cdx genes, may be important factors for the development of IM.

Toshikazu Ushijima - One of the best experts on this subject based on the ideXlab platform.

  • down regulation of a gastric transcription factor sox2 and Ectopic Expression of intestinal homeobox genes cdx1 and cdx2 inverse correlation during progression from gastric intestinal mixed to complete intestinal metaplasia
    Journal of Cancer Research and Clinical Oncology, 2004
    Co-Authors: Tetsuya Tsukamoto, Ken Ichi Inada, Harunari Tanaka, Tsutomu Mizoshita, Mami Mihara, Toshikazu Ushijima, Yoshitaka Yamamura, Shigeo Nakamura, Masae Tatematsu
    Abstract:

    Purpose The molecular mechanisms underlying the development of intestinal metaplasia (IM) of the human stomach have yet to be clarified in detail. Besides Ectopic Expression of intestinal transcription factors, Cdx1 and Cdx2, little information is available regarding other regulatory factors. Hence, we here analyzed Sox2, a human homolog of a chicken gastric transcription factor, with reference to our new classification for gastric/intestinal (GI)-mixed type IM.

  • down regulation of a gastric transcription factor sox2 and Ectopic Expression of intestinal homeobox genes cdx1 and cdx2 inverse correlation during progression from gastric intestinal mixed to complete intestinal metaplasia
    Journal of Cancer Research and Clinical Oncology, 2004
    Co-Authors: Tetsuya Tsukamoto, Ken Ichi Inada, Harunari Tanaka, Tsutomu Mizoshita, Mami Mihara, Toshikazu Ushijima, Yoshitaka Yamamura, Shigeo Nakamura, Masae Tatematsu
    Abstract:

    The molecular mechanisms underlying the development of intestinal metaplasia (IM) of the human stomach have yet to be clarified in detail. Besides Ectopic Expression of intestinal transcription factors, Cdx1 and Cdx2, little information is available regarding other regulatory factors. Hence, we here analyzed Sox2, a human homolog of a chicken gastric transcription factor, with reference to our new classification for gastric/intestinal (GI)-mixed type IM. Twenty specimens of surgically resected antral mucosa were subjected to a gland isolation technique. Isolated glands were classified into gastric (G), GI-mixed, and solely intestinal (I) types according to Alcian blue and paradoxical concanavalin A staining and were quantified for mRNA levels of gastrointestinal markers. MUC5AC and MUC6 transcripts decreased with the progression of IM, while MUC2 and villin-1 were inversely correlated. Sox2 showed a gradual decrease from G, through GI, to the I type (G vs GI and GI vs I, P<0.01 and P<0.005, respectively). On the other hand, Cdx1 (G vs GI and GI vs I, P<0.0001 and P=0.337, respectively) and Cdx2 (G vs GI and GI vs I, P<0.0001 and P<0.05, respectively) appeared in IM. Immunohistochemical study confirmed decreased Expression of Sox2 and Ectopic emergence of Cdx2 protein in IM glands. Down-regulation of Sox2, besides Ectopic Expression of Cdx genes, may be important factors for the development of IM.