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Molecular Inhibitor of QSOX1 Suppresses Tumor Growth In Vivo.
Fifield, Amber L; Hanavan, Paul D; Faigel, Douglas O; Sergienko, Eduard; Bobkov, Andrey; Meurice, Nathalie; Petit, Joachim L; Polito, Alysia; Caulfield, Thomas R; Castle, Erik P; Copland, John A; Mukhopadhyay, Debabrata; Pal, Krishnendu; Dutta, Shamit K; Luo, Huijun; Ho, Thai H; Lake, Douglas F.
Afiliação
  • Fifield AL; School of Life Sciences, Arizona State University, Tempe, Arizona.
  • Hanavan PD; RenBio, Inc., New York, New York.
  • Faigel DO; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Mayo Clinic, Phoenix, Arizona.
  • Sergienko E; Assay Development, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California.
  • Bobkov A; Assay Development, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California.
  • Meurice N; Hematology/Oncology, Mayo Clinic, Scottsdale, Arizona.
  • Petit JL; Hematology/Oncology, Mayo Clinic, Scottsdale, Arizona.
  • Polito A; Hematology/Oncology, Mayo Clinic, Scottsdale, Arizona.
  • Caulfield TR; Department of Neuroscience, Mayo Clinic, Jacksonville, Florida.
  • Castle EP; Mayo Graduate School, Neurobiology of Disease, Mayo Clinic, Jacksonville, Florida.
  • Copland JA; Department of Cancer Biology, Mayo Clinic, Jacksonville, Florida.
  • Mukhopadhyay D; Health Sciences Research, Division of Biomedical Statistics & Informatics, Mayo Clinic, Jacksonville, Florida.
  • Pal K; Center for Individualized Medicine, Mayo Clinic, Jacksonville, Florida.
  • Dutta SK; Department of Urology, Mayo Clinic, Phoenix, Arizona.
  • Luo H; Department of Cancer Biology, Mayo Clinic, Jacksonville, Florida.
  • Ho TH; Department of Biochemistry and Molecular Biology, Mayo Clinic, Jacksonville, Florida.
  • Lake DF; Department of Biochemistry and Molecular Biology, Mayo Clinic, Jacksonville, Florida.
Mol Cancer Ther ; 19(1): 112-122, 2020 01.
Article em En | MEDLINE | ID: mdl-31575656
ABSTRACT
Quiescin sulfhydryl oxidase 1 (QSOX1) is an enzyme overexpressed by many different tumor types. QSOX1 catalyzes the formation of disulfide bonds in proteins. Because short hairpin knockdowns (KD) of QSOX1 have been shown to suppress tumor growth and invasion in vitro and in vivo, we hypothesized that chemical compounds inhibiting QSOX1 enzymatic activity would also suppress tumor growth, invasion, and metastasis. High throughput screening using a QSOX1-based enzymatic assay revealed multiple potential QSOX1 inhibitors. One of the inhibitors, known as "SBI-183," suppresses tumor cell growth in a Matrigel-based spheroid assay and inhibits invasion in a modified Boyden chamber, but does not affect viability of nonmalignant cells. Oral administration of SBI-183 inhibits tumor growth in 2 independent human xenograft mouse models of renal cell carcinoma. We conclude that SBI-183 warrants further exploration as a useful tool for understanding QSOX1 biology and as a potential novel anticancer agent in tumors that overexpress QSOX1.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regulação Neoplásica da Expressão Gênica / Oxirredutases atuantes sobre Doadores de Grupo Enxofre / Neoplasias Renais Limite: Animals / Female / Humans Idioma: En Revista: Mol Cancer Ther Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regulação Neoplásica da Expressão Gênica / Oxirredutases atuantes sobre Doadores de Grupo Enxofre / Neoplasias Renais Limite: Animals / Female / Humans Idioma: En Revista: Mol Cancer Ther Ano de publicação: 2020 Tipo de documento: Article