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TCF21 inhibits tumor-associated angiogenesis and suppresses the growth of cholangiocarcinoma by targeting PI3K/Akt and ERK signaling.
Duan, Hua-Xin; Li, Bo-Wen; Zhuang, Xin; Wang, Lu-Ting; Cao, Qian; Tan, Ling-Hua; Qu, Gui-Fang; Xiao, Shuang.
Afiliação
  • Duan HX; Department of Oncology, Hunan Provincial People's Hospital and the First Affiliated Hospital of Hunan Normal University , Changsha , People's Republic of China; and Key Laboratory of Study and Discovery of Small Targeted Molecules of Hunan Province, Changsha, Hunan, People's Republic of China.
  • Li BW; Department of Oncology, Hunan Provincial People's Hospital and the First Affiliated Hospital of Hunan Normal University , Changsha , People's Republic of China; and Key Laboratory of Study and Discovery of Small Targeted Molecules of Hunan Province, Changsha, Hunan, People's Republic of China.
  • Zhuang X; Department of Oncology, Hunan Provincial People's Hospital and the First Affiliated Hospital of Hunan Normal University , Changsha , People's Republic of China; and Key Laboratory of Study and Discovery of Small Targeted Molecules of Hunan Province, Changsha, Hunan, People's Republic of China.
  • Wang LT; Department of Oncology, Hunan Provincial People's Hospital and the First Affiliated Hospital of Hunan Normal University , Changsha , People's Republic of China; and Key Laboratory of Study and Discovery of Small Targeted Molecules of Hunan Province, Changsha, Hunan, People's Republic of China.
  • Cao Q; Department of Oncology, Hunan Provincial People's Hospital and the First Affiliated Hospital of Hunan Normal University , Changsha , People's Republic of China; and Key Laboratory of Study and Discovery of Small Targeted Molecules of Hunan Province, Changsha, Hunan, People's Republic of China.
  • Tan LH; Department of Oncology, Hunan Provincial People's Hospital and the First Affiliated Hospital of Hunan Normal University , Changsha , People's Republic of China; and Key Laboratory of Study and Discovery of Small Targeted Molecules of Hunan Province, Changsha, Hunan, People's Republic of China.
  • Qu GF; Department of Oncology, Hunan Provincial People's Hospital and the First Affiliated Hospital of Hunan Normal University , Changsha , People's Republic of China; and Key Laboratory of Study and Discovery of Small Targeted Molecules of Hunan Province, Changsha, Hunan, People's Republic of China.
  • Xiao S; Department of Oncology, Hunan Provincial People's Hospital and the First Affiliated Hospital of Hunan Normal University , Changsha , People's Republic of China; and Key Laboratory of Study and Discovery of Small Targeted Molecules of Hunan Province, Changsha, Hunan, People's Republic of China.
Am J Physiol Gastrointest Liver Physiol ; 316(6): G763-G773, 2019 06 01.
Article em En | MEDLINE | ID: mdl-30920845
Tumor-associated angiogenesis plays a critical role in the pathogenesis of cholangiocarcinoma (CCA). In this study, we examined the biological effects and molecular mechanisms of transcription factor 21 (TCF21) on CCA-associated angiogenesis. TCF21 expression was compared between 15 pairs of peritumor normal tissues and CCA tissues and also between normal bile duct epithelial cells and two CCA cell lines (QBC-939 and TFK-1) using real-time PCR and Western blot. With the use of both CCA cell lines as the model system, we stably expressed TCF21 by lentiviral transduction (Lv-TCF21). In vivo, we monitored xenograft growth from different CCA cells, measured tumor-associated angiogenesis by histological analysis, and determined the expressions and circulatory levels of VEGFA and PDGF-BB by immunohistochemistry and ELISA, respectively. In vitro, we assessed the effects of conditioned medium collected from different CCA cells on the viability, migration, and tube formation of endothelial cells and explored the significance of phosphatidylinositol 3-kinase/protein kinase B (PI3K/Akt), as well as ERK1/2 signaling in this process. TCF21 was significantly downregulated in CCA tissues or cell lines. Ectopic expression of TCF21 in CCA cells inhibited xenograft growth or tumor-associated angiogenesis in vivo and targeted the expression and secretion of proangiogenic factors, VEGFA and PDGF-BB. In vitro, the conditioned medium collected from Lv-TCF21 CCA cells significantly reduced the viability, migration, and tube formation of endothelial cells. On the molecular level, the targeting of PI3K/Akt and ERK1/2 signaling mediated the anti-angiogenic activity of TCF21. TCF21 presents growth-inhibitory and anti-angiogenic activities, and thus the elevation of TCF21 expression may provide therapeutic benefits for CCA. NEW & NOTEWORTHY Transcription factor 21 (TCF21) is downregulated in cholangiocarcinoma (CCA) tissues or cells. TCF21 inhibits the growth of xenografts derived from CCA cells. TCF21 suppresses in vivo tumor-associated angiogenesis. TCF21 targets expression and production of proangiogenic factors from CCA cells. The targeting of phosphatidylinositol 3-kinase/protein kinase B and ERK1/2 signaling mediates the anti-angiogenesis of TCF21.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias dos Ductos Biliares / Colangiocarcinoma / Fatores de Transcrição Hélice-Alça-Hélice Básicos / Neovascularização Patológica Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias dos Ductos Biliares / Colangiocarcinoma / Fatores de Transcrição Hélice-Alça-Hélice Básicos / Neovascularização Patológica Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article