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1.
Vet Comp Oncol ; 16(4): 459-466, 2018 Dec.
Article in English | MEDLINE | ID: mdl-29797768

ABSTRACT

Intracranial gliomas are a common malignancy in dogs, and are associated with a poor prognosis due to their aggressive nature and a lack of clinically effective treatments. The efficacies of various treatment modalities for canine brain tumours have been previously described, though little data exist on the use of cytotoxic chemotherapy. A comparative retrospective study, including 40 cases from 5 northeastern US veterinary hospitals, from 2008 to 2017, was conducted. Variables analysed in this study with relation to overall survival and prognostic significance included: age, sex, clinical signs, clinical sign duration, tumour location and treatment protocol used. Dogs with presumptive intracranial gliomas treated with lomustine chemotherapy lived longer (median, 138 days) than those treated exclusively with symptomatic care (median, 35 days; P = .0026 log-rank, 0.0138 Wilcoxon). Additionally, a duration of clinical signs ≥16 days prior to diagnosis (median, 109 days) was associated with a longer survival than a duration <16 days prior (median, 25 days; P = .0100 log-rank, 0.0322 Wilcoxon). Lomustine-associated side effects included neutropenia in 46% of dogs, anaemia in 15% and thrombocytopenia in 15%. Potential renal and hepatotoxicity based on increased BUN and/or creatinine and ALT values were reported in 15% and 50% of dogs, respectively. This study provides evidence that lomustine therapy may be effective in prolonging survival in dogs with intracranial gliomas and should be considered as a potential treatment option. Although lomustine-related toxicities are fairly common, they are rarely life threatening and often do not result in discontinuation of therapy.


Subject(s)
Antineoplastic Agents, Alkylating/therapeutic use , Brain Neoplasms/veterinary , Dog Diseases/drug therapy , Glioma/veterinary , Lomustine/therapeutic use , Administration, Oral , Animals , Antineoplastic Agents, Alkylating/administration & dosage , Brain Neoplasms/drug therapy , Brain Neoplasms/mortality , Dog Diseases/mortality , Dogs , Female , Glioma/drug therapy , Glioma/mortality , Lomustine/administration & dosage , Male , Retrospective Studies , Survival Analysis
2.
EMBO J ; 17(5): 1192-9, 1998 Mar 02.
Article in English | MEDLINE | ID: mdl-9482716

ABSTRACT

The tetratricopeptide repeat (TPR) is a degenerate 34 amino acid sequence identified in a wide variety of proteins, present in tandem arrays of 3-16 motifs, which form scaffolds to mediate protein-protein interactions and often the assembly of multiprotein complexes. TPR-containing proteins include the anaphase promoting complex (APC) subunits cdc16, cdc23 and cdc27, the NADPH oxidase subunit p67 phox, hsp90-binding immunophilins, transcription factors, the PKR protein kinase inhibitor, and peroxisomal and mitochondrial import proteins. Here, we report the crystal structure of the TPR domain of a protein phosphatase, PP5. Each of the three TPR motifs of this domain consist of a pair of antiparallel alpha-helices of equivalent length. Adjacent TPR motifs are packed together in a parallel arrangement such that a tandem TPR motif structure is composed of a regular series of antiparallel alpha-helices. The uniform angular and spatial arrangement of neighbouring alpha-helices defines a helical structure and creates an amphipathic groove. Multiple-TPR motif proteins would fold into a right-handed super-helical structure with a continuous helical groove suitable for the recognition of target proteins, hence defining a novel mechanism for protein recognition. The spatial arrangement of alpha-helices in the PP5-TPR domain is similar to those within 14-3-3 proteins.


Subject(s)
Nuclear Proteins/chemistry , Phosphoprotein Phosphatases/chemistry , Protein Structure, Secondary , Tyrosine 3-Monooxygenase , 14-3-3 Proteins , Amino Acid Sequence , Crystallography, X-Ray , Humans , Models, Molecular , Molecular Sequence Data , Peptides/chemistry , Proteins/chemistry , Sequence Alignment
3.
Community Ment Health J ; 20(4): 304-12, 1984.
Article in English | MEDLINE | ID: mdl-6518743

ABSTRACT

We conducted a telephone survey in three boroughs of New York City to assess the impact of proximity to psychiatric facilities on attitudes toward the mentally ill. Six pairs of areas were selected for sampling; within pairs, one area included a facility serving chronically ill psychiatric patients and the other contained no health or mental health facility. Three-quarters of those living within a block of the selected facilities were found to be unaware of their presence. Further, attitudes toward mental illness and patients were not related to proximity to such facilities. These results cumulatively suggest that community psychiatric facilities do not necessarily constitute a personal or community burden as far as the neighbors are concerned.


Subject(s)
Attitude , Community Mental Health Centers , Community-Institutional Relations , Mental Disorders/therapy , Humans , Mental Disorders/psychology , New York City , Social Desirability , Social Environment
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