scholarly journals ANN Multiscale Model of Anti-HIV Drugs Activity vs AIDS Prevalence in the US at County Level Based on Information Indices of Molecular Graphs and Social Networks

2014 ◽  
Vol 54 (3) ◽  
pp. 744-755 ◽  
Author(s):  
Humberto González-Díaz ◽  
Diana María Herrera-Ibatá ◽  
Aliuska Duardo-Sánchez ◽  
Cristian R. Munteanu ◽  
Ricardo Alfredo Orbegozo-Medina ◽  
...  
2015 ◽  
Vol 10 (5) ◽  
pp. 639-657 ◽  
Author(s):  
Diana Maria Herrera-Ibata ◽  
Ricardo Alfredo Orbegozo-Medina ◽  
Humberto Gonzalez-Diaz

2012 ◽  
Vol 93 (4) ◽  
pp. 900-905 ◽  
Author(s):  
Willie M. Greggs ◽  
Christine L. Clouser ◽  
Steven E. Patterson ◽  
Louis M. Mansky

Feline leukemia virus (FeLV) is a gammaretrovirus that is a significant cause of neoplastic-related disorders affecting cats worldwide. Treatment options for FeLV are limited, associated with serious side effects, and can be cost-prohibitive. The development of drugs used to treat a related retrovirus, human immunodeficiency virus type 1 (HIV-1), has been rapid, leading to the approval of five drug classes. Although structural differences affect the susceptibility of gammaretroviruses to anti-HIV drugs, the similarities in mechanism of replication suggest that some anti-HIV-1 drugs may also inhibit FeLV. This study demonstrates the anti-FeLV activity of four drugs approved by the US FDA (Food and Drug Administration) at non-toxic concentrations. Of these, tenofovir and raltegravir are anti-HIV-1 drugs, while decitabine and gemcitabine are approved to treat myelodysplastic syndromes and pancreatic cancer, respectively, but also have anti-HIV-1 activity in cell culture. Our results indicate that these drugs may be useful for FeLV treatment and should be investigated for mechanism of action and suitability for veterinary use.


2012 ◽  
Vol 31 (3) ◽  
pp. 211-221 ◽  
Author(s):  
Kuei-Meng Wu ◽  
Mark W. Powley ◽  
Hanan Ghantous

The timing of carcinogenicity studies in parallel with the clinical development of anti–human immunodeficiency virus (HIV) drugs has been flexible for most cases in the past. This includes postponement of the initiation of the studies and submission of final audited reports to the US Food and Drug Administration (FDA) for a new drug application (NDA) approval. We address this regulatory practice for anti-HIV drugs for which, in the past, there had been no effective treatment. We also examine the correlation of genotoxicity data with carcinogenicity data for the varied subclasses of anti-HIV drugs. We suggest that this regulatory policy regarding the timing of carcinogenicity testing does not compromise the safety standards of FDA’s drug evaluation and the approval process. The policy does facilitate availability of these agents to meet the medical needs of the target population. Our analysis on the profile of carcinogenicity findings of anti-HIV drugs shows trends of class effects. Additionally, both carcinogenicity and genotoxicity data show significant correlations, which provide useful insights into issues involving these 2 important areas of toxicological investigations.


2005 ◽  
Vol 35 (3) ◽  
pp. 32
Author(s):  
MITCHEL L. ZOLER
Keyword(s):  

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