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Mitochondrial pyruvate carrier 1 expression controls cancer epithelial-mesenchymal transition and radioresistance.
Takaoka, Yuji; Konno, Masamitsu; Koseki, Jun; Colvin, Hugh; Asai, Ayumu; Tamari, Keisuke; Satoh, Taroh; Mori, Masaki; Doki, Yuichiro; Ogawa, Kazuhiko; Ishii, Hideshi.
Afiliación
  • Takaoka Y; Department of Radiation Oncology, Osaka University, Suita, Japan.
  • Konno M; Department of Medical Data Science, Osaka University, Suita, Japan.
  • Koseki J; Department of Frontier Science for Cancer and Chemotherapy, Osaka University, Osaka, Japan.
  • Colvin H; Department of Medical Data Science, Osaka University, Suita, Japan.
  • Asai A; Department of Medical Data Science, Osaka University, Suita, Japan.
  • Tamari K; Department of Frontier Science for Cancer and Chemotherapy, Osaka University, Osaka, Japan.
  • Satoh T; Department of Medical Data Science, Osaka University, Suita, Japan.
  • Mori M; Department of Radiation Oncology, Osaka University, Suita, Japan.
  • Doki Y; Department of Frontier Science for Cancer and Chemotherapy, Osaka University, Osaka, Japan.
  • Ogawa K; Department of Gastroenterological Surgery, Osaka University, Suita, Japan.
  • Ishii H; Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Cancer Sci ; 110(4): 1331-1339, 2019 Apr.
Article en En | MEDLINE | ID: mdl-30801869
ABSTRACT
Mitochondrial pyruvate carrier (MPC) is known to cause different expressions in normal and cancer cells. We observed a change in phenotype with the suppression of MPC expression. We knocked down MPC1 and/or MPC2 using siRNA or shRNA. We observed its cell morphology and accompanying molecular marker. Furthermore, the radioresistance of the MPC knockdown cell line was examined using a colony formation assay. MPC1-suppressed cells changed their morphology to a spindle shape. Epithelial-mesenchymal transition (EMT) was suspected, and examination of the EMT marker by PCR showed a decrease in E-cadherin and an increase in fibronectin. Focusing on glutamine metabolism as the mechanism of this phenomenon, we knocked down the glutamine-metabolizing enzyme glutaminase (GLS). EMT was also observed in GLS-suppressed cells. Furthermore, when MPC1-suppressed cells were cultured in a glutamine-deficient medium, changes in EMT markers were suppressed. In addition, MPC1-suppressed cells also increased with a significant difference in radioresistance. Decreased MPC1 expression favorably affects EMT and radioresistance of cancer.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Tolerancia a Radiación / Regulación Neoplásica de la Expresión Génica / Proteínas de Transporte de Membrana Mitocondrial / Transición Epitelial-Mesenquimal / Neoplasias Límite: Humans Idioma: En Revista: Cancer Sci Año: 2019 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Tolerancia a Radiación / Regulación Neoplásica de la Expresión Génica / Proteínas de Transporte de Membrana Mitocondrial / Transición Epitelial-Mesenquimal / Neoplasias Límite: Humans Idioma: En Revista: Cancer Sci Año: 2019 Tipo del documento: Article País de afiliación: Japón