Transcription factor LSF (TFCP2) inhibits melanoma growth

Yuji Goto, Ichiro Yajima, Mayuko Kumasaka, Nobutaka Ohgami, Asami Tanaka, Toyonori Tsuzuki, Yuji Inoue, Satoshi Fukushima, Hironobu Ihn, Mikiko Kyoya, Hiroyuki Ohashi, Tamihiro Kawakami, Dorothy C. Bennett, Masashi Kato

研究成果: Article

11 引用 (Scopus)

抄録

Late SV40 factor 3 (LSF), a transcription factor, contributes to human hepatocellular carcinoma (HCC). However, decreased expression level of LSF in skin melanoma compared to that in benign melanocytic tumors and nevi in mice and humans was found in this study. Anchorage-dependent and -independent growth of melanoma cells was suppressed by LSF overexpression through an increased percentage of G1 phase cells and an increased p21CIP1 expression level in vitro and in vivo. Anchorage-dependent growth in LSF-overexpressed melanoma cells was promoted by depletion of LSF in the LSF-overexpressed cells. Integrated results of our EMSA and chromatin immunoprecipitation assays showed binding of LSF within a 150-bp upstream region of the transcription start site of p21CIP1 in melanoma cells. Taken together, our results suggest potential roles of LSF as a growth regulator through control of the transcription of p21CIP1 in melanocytes and melanoma cells as well as a biomarker for nevus.

元の言語English
ページ(範囲)2379-2390
ページ数12
ジャーナルOncotarget
7
発行部数3
DOI
出版物ステータスPublished - 2016 1 1
外部発表Yes

ASJC Scopus subject areas

  • Oncology

これを引用

Goto, Y., Yajima, I., Kumasaka, M., Ohgami, N., Tanaka, A., Tsuzuki, T., ... Kato, M. (2016). Transcription factor LSF (TFCP2) inhibits melanoma growth. Oncotarget, 7(3), 2379-2390. https://doi.org/10.18632/oncotarget.6230

Transcription factor LSF (TFCP2) inhibits melanoma growth. / Goto, Yuji; Yajima, Ichiro; Kumasaka, Mayuko; Ohgami, Nobutaka; Tanaka, Asami; Tsuzuki, Toyonori; Inoue, Yuji; Fukushima, Satoshi; Ihn, Hironobu; Kyoya, Mikiko; Ohashi, Hiroyuki; Kawakami, Tamihiro; Bennett, Dorothy C.; Kato, Masashi.

:: Oncotarget, 巻 7, 番号 3, 01.01.2016, p. 2379-2390.

研究成果: Article

Goto, Y, Yajima, I, Kumasaka, M, Ohgami, N, Tanaka, A, Tsuzuki, T, Inoue, Y, Fukushima, S, Ihn, H, Kyoya, M, Ohashi, H, Kawakami, T, Bennett, DC & Kato, M 2016, 'Transcription factor LSF (TFCP2) inhibits melanoma growth', Oncotarget, 巻. 7, 番号 3, pp. 2379-2390. https://doi.org/10.18632/oncotarget.6230
Goto Y, Yajima I, Kumasaka M, Ohgami N, Tanaka A, Tsuzuki T その他. Transcription factor LSF (TFCP2) inhibits melanoma growth. Oncotarget. 2016 1 1;7(3):2379-2390. https://doi.org/10.18632/oncotarget.6230
Goto, Yuji ; Yajima, Ichiro ; Kumasaka, Mayuko ; Ohgami, Nobutaka ; Tanaka, Asami ; Tsuzuki, Toyonori ; Inoue, Yuji ; Fukushima, Satoshi ; Ihn, Hironobu ; Kyoya, Mikiko ; Ohashi, Hiroyuki ; Kawakami, Tamihiro ; Bennett, Dorothy C. ; Kato, Masashi. / Transcription factor LSF (TFCP2) inhibits melanoma growth. :: Oncotarget. 2016 ; 巻 7, 番号 3. pp. 2379-2390.
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abstract = "Late SV40 factor 3 (LSF), a transcription factor, contributes to human hepatocellular carcinoma (HCC). However, decreased expression level of LSF in skin melanoma compared to that in benign melanocytic tumors and nevi in mice and humans was found in this study. Anchorage-dependent and -independent growth of melanoma cells was suppressed by LSF overexpression through an increased percentage of G1 phase cells and an increased p21CIP1 expression level in vitro and in vivo. Anchorage-dependent growth in LSF-overexpressed melanoma cells was promoted by depletion of LSF in the LSF-overexpressed cells. Integrated results of our EMSA and chromatin immunoprecipitation assays showed binding of LSF within a 150-bp upstream region of the transcription start site of p21CIP1 in melanoma cells. Taken together, our results suggest potential roles of LSF as a growth regulator through control of the transcription of p21CIP1 in melanocytes and melanoma cells as well as a biomarker for nevus.",
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AU - Goto, Yuji

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AU - Kumasaka, Mayuko

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AU - Tanaka, Asami

AU - Tsuzuki, Toyonori

AU - Inoue, Yuji

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AU - Ihn, Hironobu

AU - Kyoya, Mikiko

AU - Ohashi, Hiroyuki

AU - Kawakami, Tamihiro

AU - Bennett, Dorothy C.

AU - Kato, Masashi

PY - 2016/1/1

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N2 - Late SV40 factor 3 (LSF), a transcription factor, contributes to human hepatocellular carcinoma (HCC). However, decreased expression level of LSF in skin melanoma compared to that in benign melanocytic tumors and nevi in mice and humans was found in this study. Anchorage-dependent and -independent growth of melanoma cells was suppressed by LSF overexpression through an increased percentage of G1 phase cells and an increased p21CIP1 expression level in vitro and in vivo. Anchorage-dependent growth in LSF-overexpressed melanoma cells was promoted by depletion of LSF in the LSF-overexpressed cells. Integrated results of our EMSA and chromatin immunoprecipitation assays showed binding of LSF within a 150-bp upstream region of the transcription start site of p21CIP1 in melanoma cells. Taken together, our results suggest potential roles of LSF as a growth regulator through control of the transcription of p21CIP1 in melanocytes and melanoma cells as well as a biomarker for nevus.

AB - Late SV40 factor 3 (LSF), a transcription factor, contributes to human hepatocellular carcinoma (HCC). However, decreased expression level of LSF in skin melanoma compared to that in benign melanocytic tumors and nevi in mice and humans was found in this study. Anchorage-dependent and -independent growth of melanoma cells was suppressed by LSF overexpression through an increased percentage of G1 phase cells and an increased p21CIP1 expression level in vitro and in vivo. Anchorage-dependent growth in LSF-overexpressed melanoma cells was promoted by depletion of LSF in the LSF-overexpressed cells. Integrated results of our EMSA and chromatin immunoprecipitation assays showed binding of LSF within a 150-bp upstream region of the transcription start site of p21CIP1 in melanoma cells. Taken together, our results suggest potential roles of LSF as a growth regulator through control of the transcription of p21CIP1 in melanocytes and melanoma cells as well as a biomarker for nevus.

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