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Quinolinate Phosphoribosyltransferase Promotes Invasiveness of Breast Cancer Through Myosin Light Chain Phosphorylation.
Liu, Chien-Liang; Cheng, Shih-Ping; Chen, Ming-Jen; Lin, Chi-Hsin; Chen, Shan-Na; Kuo, Yi-Hue; Chang, Yuan-Ching.
Afiliação
  • Liu CL; Department of Surgery, MacKay Memorial Hospital, Taipei, Taiwan.
  • Cheng SP; Department of Surgery, School of Medicine, Mackay Medical College, New Taipei City, Taiwan.
  • Chen MJ; Department of Medical Research, MacKay Memorial Hospital, Taipei, Taiwan.
  • Lin CH; Department of Surgery, MacKay Memorial Hospital, Taipei, Taiwan.
  • Chen SN; Department of Surgery, School of Medicine, Mackay Medical College, New Taipei City, Taiwan.
  • Kuo YH; Department of Medical Research, MacKay Memorial Hospital, Taipei, Taiwan.
  • Chang YC; Department of Surgery, MacKay Memorial Hospital, Taipei, Taiwan.
Front Endocrinol (Lausanne) ; 11: 621944, 2020.
Article em En | MEDLINE | ID: mdl-33613454
ABSTRACT
Perturbed Nicotinamide adenine dinucleotide (NAD+) homeostasis is involved in cancer progression and metastasis. Quinolinate phosphoribosyltransferase (QPRT) is the rate-limiting enzyme in the kynurenine pathway participating in NAD+ generation. In this study, we demonstrated that QPRT expression was upregulated in invasive breast cancer and spontaneous mammary tumors from MMTV-PyVT transgenic mice. Knockdown of QPRT expression inhibited breast cancer cell migration and invasion. Consistently, ectopic expression of QPRT promoted cell migration and invasion in breast cancer cells. Treatment with QPRT inhibitor (phthalic acid) or P2Y11 antagonist (NF340) could reverse the QPRT-induced invasiveness and phosphorylation of myosin light chain. Similar reversibility could be observed following treatment with Rho inhibitor (Y16), ROCK inhibitor (Y27632), PLC inhibitor (U73122), or MLCK inhibitor (ML7). Altogether, these results indicate that QPRT enhanced breast cancer invasiveness probably through purinergic signaling and might be a potential prognostic indicator and therapeutic target in breast cancer.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Pentosiltransferases / Neoplasias da Mama / Movimento Celular / Cadeias Leves de Miosina Limite: Animals / Female / Humans Idioma: En Revista: Front Endocrinol (Lausanne) Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Taiwan

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Pentosiltransferases / Neoplasias da Mama / Movimento Celular / Cadeias Leves de Miosina Limite: Animals / Female / Humans Idioma: En Revista: Front Endocrinol (Lausanne) Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Taiwan