Assessing Metabolic Changes in Response to mTOR Inhibition in a Mantle Cell Lymphoma Xenograft Model Using AcidoCEST MRI.

Autor: Akhenblit PJ; Cancer Biology Graduate Interdisciplinary Program, University of Arizona, Tucson, AZ, USA., Hanke NT; University of Arizona Cancer Center, University of Arizona, Tucson, AZ, USA., Gill A; University of Arizona Cancer Center, University of Arizona, Tucson, AZ, USA., Persky DO; University of Arizona Cancer Center, University of Arizona, Tucson, AZ, USA., Howison CM; Department of Medical Imaging, University of Arizona, Tucson, AZ, USA., Pagel MD; Cancer Biology Graduate Interdisciplinary Program, University of Arizona, Tucson, AZ, USA University of Arizona Cancer Center, University of Arizona, Tucson, AZ, USA Department of Medical Imaging, University of Arizona, Tucson, AZ, USA., Baker AF; University of Arizona Cancer Center, University of Arizona, Tucson, AZ, USA abaker@uacc.arizona.edu.

Publikováno v: Molecular imaging [Mol Imaging] 2016 May 02; Vol. 15. Date of Electronic Publication: 2016 May 02 (Print Publication: 2016).

The anti-tumor efficacy of 2-deoxyglucose and D-allose are enhanced with p38 inhibition in pancreatic and ovarian cell lines.

Autor: Malm SW; College of Pharmacy, University of Arizona, Tucson, Arizona, USA. malm@pharmacy.arizona.edu., Hanke NT; College of Medicine, University of Arizona Cancer Center, Tucson, Arizona, USA. nhanke@email.arizona.edu., Gill A; College of Medicine, University of Arizona Cancer Center, Tucson, Arizona, USA. alex2@email.arizona.edu., Carbajal L; College of Medicine, University of Arizona Cancer Center, Tucson, Arizona, USA. lili.carbajal@gmail.com., Baker AF; College of Medicine, University of Arizona Cancer Center, Tucson, Arizona, USA. abaker@uacc.arizona.edu.

Publikováno v: Journal of experimental & clinical cancer research : CR [J Exp Clin Cancer Res] 2015 Apr 01; Vol. 34, pp. 31. Date of Electronic Publication: 2015 Apr 01.

PIAS1 and STAT-3 impair the tumoricidal potential of IFN-γ-stimulated mouse dendritic cells generated with IL-15.

Autor: Hanke NT; Department of Pediatrics, University of Arizona, Tucson, AZ, United States of America.; Cancer Biology Graduate Interdisciplinary Program, University of Arizona, Tucson, AZ, United States of America., LaCasse CJ; Department of Pediatrics, University of Arizona, Tucson, AZ, United States of America.; Cancer Biology Graduate Interdisciplinary Program, University of Arizona, Tucson, AZ, United States of America., Larmonier CB; Department of Pediatrics, University of Arizona, Tucson, AZ, United States of America., Alizadeh D; Department of Pediatrics, University of Arizona, Tucson, AZ, United States of America.; Cancer Biology Graduate Interdisciplinary Program, University of Arizona, Tucson, AZ, United States of America., Trad M; INSERM UMR 1098, Faculty of Medicine, Dijon, France., Janikashvili N; INSERM UMR 1098, Faculty of Medicine, Dijon, France., Bonnotte B; INSERM UMR 1098, Faculty of Medicine, Dijon, France., Katsanis E; Department of Pediatrics, University of Arizona, Tucson, AZ, United States of America.; Cancer Biology Graduate Interdisciplinary Program, University of Arizona, Tucson, AZ, United States of America.; Department of Immunobiology, BIO5 Institute and Arizona Cancer Center, University of Arizona, Tucson, AZ, United States of America., Larmonier N; Department of Pediatrics, University of Arizona, Tucson, AZ, United States of America.; Cancer Biology Graduate Interdisciplinary Program, University of Arizona, Tucson, AZ, United States of America.; Department of Immunobiology, BIO5 Institute and Arizona Cancer Center, University of Arizona, Tucson, AZ, United States of America.

Publikováno v: European journal of immunology [Eur J Immunol] 2014 Aug; Vol. 44 (8), pp. 2489-2499. Date of Electronic Publication: 2014 May 23.

Myeloid-derived suppressor cells from tumor-bearing mice impair TGF-β-induced differentiation of CD4+CD25+FoxP3+ Tregs from CD4+CD25-FoxP3- T cells.

Autor: Centuori SM; Department of Pediatrics, College of Medicine, University of Arizona, Tucson, AZ 85724-5073, USA., Trad M, LaCasse CJ, Alizadeh D, Larmonier CB, Hanke NT, Kartchner J, Janikashvili N, Bonnotte B, Larmonier N, Katsanis E

Publikováno v: Journal of leukocyte biology [J Leukoc Biol] 2012 Nov; Vol. 92 (5), pp. 987-97. Date of Electronic Publication: 2012 Aug 13.

Loss of catalase increases malignant mouse keratinocyte cell growth through activation of the stress activated JNK pathway.

Autor: Hanke NT; Arizona Cancer Center, University of Arizona, Tucson, AZ 85724-5024, USA., Finch JS, Bowden GT

Publikováno v: Molecular carcinogenesis [Mol Carcinog] 2008 May; Vol. 47 (5), pp. 349-60.