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Dive into the research topics where Dante Cáceres is active.

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Featured researches published by Dante Cáceres.


Cancer Letters | 2001

CYP1A1, CYP2E1 and GSTM1 genetic polymorphisms. The effect of single and combined genotypes on lung cancer susceptibility in Chilean people.

Luis Quiñones; D Lucas; J Godoy; Dante Cáceres; F Berthou; N Varela; K Lee; C Acevedo; L Martı́nez; A.M Aguilera; L Gil

CYP1A1, CYP2E1 and GSTM1 polymorphisms were evaluated in Chilean healthy controls and lung cancer patients. In the Chilean healthy group, frequencies of CYP1A1 variant alleles for MspI (m2 or CYP1A1*2A) and ile/val (val or CYP1A1*2B) polymorphisms were 0.25 and 0.33, respectively. Frequencies of variant alleles C (CYP2E1*6) and c2 (CYP2E1*5B) for CYP2E1 were 0.21 and 0.16, respectively and frequency for GSTM1(-) was 0.24. The presence of variant alleles for GSTM1, MspI and Ile/val polymorphisms was more frequent in cases than in controls. However, frequencies for the c2 and C alleles were not significantly different in controls and in cases. The estimated relative risk for lung cancer associated to a single mutated allele in CYP1A1, CYP2E1 or GSTM1 was 2.41 for m2, 1.69 for val, 1.16 for C, 0.71 for c2 and 2.46 for GSTM1(-). The estimated relative risk was higher for individuals carrying combined CYP1A1 and GSTM1 mutated alleles (m2/val, OR=6.28; m2/GSTM1(-), OR=3.56) and lower in individuals carrying CYP1A1 and CYP2E1 mutated alleles (m2/C, OR=1.39; m2/c2, OR=2.00; val/C, OR=1.45; val/c2, OR=0.48; not significant). The OR values considering smoking were 4.37 for m2, 4.05 for val, 3.47 for GSTM1(-), 7.38 for m2/val and 3.68 for m2/GSTM1(-), higher values than those observed without any stratification by smoking. Taken together, these findings suggest that Chilean people carrying single or combined GSTM1 and CYP1A1 polymorphisms could be more susceptible to lung cancer induced by environmental pollutants such as polycyclic aromatic hydrocarbons.


Phytomedicine | 1999

Use of visual analogue scale measurements (VAS) to asses the effectiveness of standardized Andrographis paniculata extract SHA-10 in reducing the symptoms of common cold. A randomized double blind-placebo study

Dante Cáceres; J.L. Hancke; Rafael A. Burgos; F. Sandberg; G.K. Wikman

The objective of our study was to measure the effectiveness of Andrographis paniculata SHA-10 extract in reducing the prevalence and intensity of symptoms and signs of common cold as compared with a placebo. A group of 158 adult patients of both sexes completed the randomized double blind study in Valdivia, Chile. The patients were divided in two equal size groups, one of which received Andrographis paniculata dried extract (1200 mg/day) and the other a placebo during a period of 5 days. Evaluations for efficacy were performed by the patient at day 0, 2, and 4 of the treatment; each completed a self-evaluation (VAS) sheet with the following parameters: headache, tiredness, earache, sleeplessness, sore throat, nasal secretion, phlegm, frequency and intensity of cough. In order to quantify the magnitude of the reduction in the prevalence and intensity of the signs and symptoms of common cold, the risk (Odds Ratio = OR) was calculated using a logistic regression model. At day 2 of treatment a significant decrease in the intensity of the symptoms of tiredness (OR = 1.28; 95% CI 1.07-1.53), sleeplessness (OR = 1.71; 95% CI 1.38-2.11), sore throat (OR = 2.3; 95% CI 1.69-3.14) and nasal secretion (OR = 2.51; 95% CI 1.82-3.46) was observed in the Andrographis SHA-10 group as compared with the placebo group. At day 4, a significant decrease in the intensity of all symptoms was observed for the Andrographis paniculata group. The higher OR values were for the following parameters: sore throat (OR = 3.59; 95% CI 2.04-5.35), nasal secretion (OR = 3.27; 95% CI 2.31-4.62) and earache (OR = 3.11; 95% CI 2.01-4.80) for Andrographis paniculata treatment over placebo, respectively. It is concluded that Andrographis paniculata had a high degree of effectiveness in reducing the prevalence and intensity of the symptoms in uncomplicated common cold beginning at day two of treatment. No adverse effects were observed or reported.


European Journal of Epidemiology | 2005

RELATIONSHIP AMONG METABOLIZING GENES, SMOKING AND ALCOHOL USED AS MODIFIER FACTORS ON PROSTATE CANCER RISK: EXPLORING SOME GENE-GENE AND GENE-ENVIRONMENT INTERACTIONS

Dante Cáceres; J Iturrieta; C Acevedo; C Huidobro; Nelson Varela; Luis Quiñones

Background: Prostate cancer (PCa) is one of the most common male cancers, but the burden of this disease shows remarkable worldwide variation. The role of susceptibility low penetrance genes and environmental factors in the etiology of (PCa) is unclear, but may involve, in some cases, multiple alleles at multiple loci and environmental factors. Study Objectives: To assess whether CYP1A1, GSTM1, GSTT1 susceptibility genotypes, smoking status and alcohol consumption factors contribute to PCa risk, gene–gene and gene–environment interactions were analyzed. Design and Participants: We explored interactions on a multiplicative scale conducting a population-based case–control and a case–only study on 103 incident PCa patients and 132 unrelated controls. Main Results: The interaction odds ratios (IOR) for PCa risk were increased in men who had both susceptibility genotypes GST (M1; T1) null andCYP1A1-M1* in a case–control and case-only design (IORcc: 1.11; 95% CI: 0.12–10.02; IORcc: 6.23; 95%, CI: 0.51–75.89; IORco: 2.80; 95% CI: 0.44–17.45 and IORco: 2.65; 95%, CI: 0.30–25.40). No clear evidence for interaction on a multiplicative scale between smoking status, alcohol consumption and genetic polymorphisms in PCa risk was observed. Conclusions: Our findings suggest that the interaction between genetic polymorphisms in GST (T1; M1) and CYP1A1-M1* would play a significant role as a modifying factor on PCa risk in Chilean people. However, these preliminary exploratory results should be confirmed in a larger study.Background: Prostate cancer (PCa) is one of the most common male cancers, but the burden of this disease shows remarkable worldwide variation. The role of susceptibility low penetrance genes and environmental factors in the etiology of (PCa) is unclear, but may involve, in some cases, multiple alleles at multiple loci and environmental factors. Study Objectives: To assess whether CYP1A1, GSTM1, GSTT1 susceptibility genotypes, smoking status and alcohol consumption factors contribute to PCa risk, gene–gene and gene–environment interactions were analyzed. Design and Participants: We explored interactions on a multiplicative scale conducting a population-based case–control and a case–only study on 103 incident PCa patients and 132 unrelated controls. Main Results: The interaction odds ratios (IOR) for PCa risk were increased in men who had both susceptibility genotypes GST (M1; T1) null and CYP1A1-M1* in a case–control and case-only design (IORcc: 1.11; 95% CI: 0.12–10.02; IORcc: 6.23; 95%, CI: 0.51–75.89; IORco: 2.80; 95% CI: 0.44–17.45 and IORco: 2.65; 95%, CI: 0.30–25.40). No clear evidence for interaction on a multiplicative scale between smoking status, alcohol consumption and genetic polymorphisms in PCa risk was observed. Conclusions: Our findings suggest that the interaction between genetic polymorphisms in GST (T1; M1) and CYP1A1-M1* would play a significant role as a modifying factor on PCa risk in Chilean people. However, these preliminary exploratory results should be confirmed in a larger study.


Frontiers in Genetics | 2012

Frequencies of 23 functionally significant variant alleles related with metabolism of antineoplastic drugs in the Chilean population: comparison with Caucasian and Asian populations

Ángela Roco; Luis Quiñones; José A. G. Agúndez; Elena García-Martín; Valentina Squicciarini; Carla Miranda; Joselyn Garay; Nancy Farfán; Iván Nicolás Pharm Saavedra; Dante Cáceres; Carol Ibarra; Nelson M. Varela

Cancer is a leading cause of death worldwide. The cancer incidence rate in Chile is 133.7/100,000 inhabitants and it is the second cause of death, after cardiovascular diseases. Most of the antineoplastic drugs are metabolized to be detoxified, and some of them to be activated. Genetic polymorphisms of drug-metabolizing enzymes can induce deep changes in enzyme activity, leading to individual variability in drug efficacy and/or toxicity. The present research describes the presence of genetic polymorphisms in the Chilean population, which might be useful in public health programs for personalized treatment of cancer, and compares these frequencies with those reported for Asian and Caucasian populations, as a contribution to the evaluation of ethnic differences in the response to chemotherapy. We analyzed 23 polymorphisms in a group of 253 unrelated Chilean volunteers from the general population. The results showed that CYP2A6*2, CYP2A6*3, CYP2D6*3, CYP2C19*3, and CYP3A4*17 variant alleles are virtually absent in Chileans. CYP1A1*2A allele frequency (0.37) is similar to that of Caucasians and higher than that reported for Japanese people. Allele frequencies for CYP3A5*3(0.76) and CYP2C9*3(0.04) are similar to those observed in Japanese people. CYP1A1*2C(0.32), CYP1A2*1F(0.77), CYP3A4*1B(0.06), CYP2D6*2(0.41), and MTHFR T(0.52) allele frequencies are higher than the observed either in Caucasian or in Japanese populations. Conversely, CYP2C19*2 allelic frequency (0.12), and genotype frequencies for GSTT1 null (0.11) and GSTM1 null (0.36) are lower than those observed in both populations. Finally, allele frequencies for CYP2A6*4(0.04), CYP2C8*3(0.06), CYP2C9*2(0.06), CYP2D6*4(0.12), CYP2E1*5B(0.14), CYP2E1*6(0.19), and UGT2B7*2(0.40) are intermediate in relation to those described in Caucasian and in Japanese populations, as expected according to the ethnic origin of the Chilean population. In conclusion, our findings support the idea that ethnic variability must be considered in the pharmacogenomic assessment of cancer pharmacotherapy, especially in mixed populations and for drugs with a narrow safety range.


Biological Research | 2008

Study of Cytochrome P450 2E1 and its allele Variants in Liver Injury of Nondiabetic, Nonalcoholic Steatohepatitis Obese Women

Nelson M. Varela; Luis Quiñones; Myriam Orellana; Jaime Poniachik; Attila Csendes; Gladys Smok; Ramón Rodrigo; Dante Cáceres; Luis A. Videla

CYP2E1 enzyme is related to nonalcoholic steatohepatitis (NASH) due to its ability for reactive oxygen species production, which can be influenced by polymorphisms in the gene. The aim of this study was to investigate hepatic levels, activity, and polymorphisms of the CYP2E1 gene to correlate it with clinical and histological features in 48 female obese NASH patients. Subjects were divided into three groups: (i) normal; (ii) steatosis; and (iii) steatohepatitis. CYP2E1 protein level was assayed in microsomes from liver biopsies, and in vivo chlorzoxazone hydroxylation was determined by HPLC. Genomic DNA was isolated for genotype analysis through PCR. The results showed that liver CYP2E1 content was significantly higher in the steatohepatitis (45%; p=0.024) and steatosis (22%; p=0.032) group compared with normal group. Chlorzoxazone hydroxylase activity showed significant enhancement in the steatohepatitis group (15%, p=0.027) compared with the normal group. c2 rare allele of RsallPstl polymorphisms but no C allele of Dral polymorphism was positively associated with CHZ hydroxylation, which in turn is correlated with liver CYP2E1 content (r=0.59; p=0.026). In conclusion, c2 allele is positively associated with liver injury in NASH. This allele may determine a higher transcriptional activity of the gene, with consequent enhancement in pro-oxidant activity of CYP2E1 thus affording liver toxicity.


Revista De Saude Publica | 2007

Early tobacco and alcohol consumption as modifying risk factors on marijuana use

Verónica Iglesias; Gabriel Cavada; Claudio Silva; Dante Cáceres

OBJECTIVE To assess the relationship between early tobacco and alcohol use and the risk of marijuana consumption among schoolchildren. METHODS A cross-sectional study comprising data from the Fourth National Study on Drug Use in the Chilean School Population (2001). There were studied 54,001 schoolchildren aged between eight and 20 years. Predictors were self-reported tobacco and alcohol use (ever users), age at initiation of tobacco and/or alcohol use, and intensity of tobacco use. The study outcome was self-reported marijuana use (ever users versus never users) and age at initiation of marijuana use. Poisson regression and Weibull regression were used for data analysis. RESULTS Lifetime prevalence of tobacco use was high: 77%, alcohol 79%, and marijuana 23%. Tobacco consumption increased the likelihood of marijuana use (PR=10.4; 95% CI: 8.9;12.2). Later initiation of tobacco (HR=0.85; 95% CI: 0.84;0.86) and alcohol (HR=0.90; 95% CI: 0.89;0.91) decreased the risk of marijuana use. Marijuana use was higher in heavy smokers compared to light smokers (PR=3.11; 95% CI: 2.96;3.26 versus PR=1.70; 95% CI: 1.58;1.83). CONCLUSIONS Tobacco use is strongly associated with marijuana use, which is significantly associated with the age at initiation of tobacco use, intensity of tobacco use and concurrent use of alcohol. Prevention strategies should target prevention of adolescent early tobacco use.


Revista Medica De Chile | 2006

Variantes alélicas de CYP1A1 y GSTM1 como biomarcadores de susceptibilidad a cáncer gástrico: influencia de los hábitos tabáquico y alcohólico

Kuen Lee; Dante Cáceres; Nelson Varela; Atila Csendes D; Horacio Ríos R; Luis Quiñones S

Gastric cancer (GaC) is the second cause of death bycancer in the world and one of the first causes in Chile. However, the burden of this disease showsremarkable worldwide variation probably explained by environmental and genetic factors. The roleof susceptibility low penetrance genes and environmental and dietary factors in the etiology ofgastric cancer is not well-known.


Revista Medica De Chile | 2006

Famacogénica del cáncer: Estudio de variaciones genéticamente determinadas en la susceptibilidad a cáncer por exposición a xenobióticos

Luis Quiñones; Kuen Lee; Nelson Varela F; Mario Escala; Karen García; Loreto Godoy; Andrés Castro; Jorge Soto; Iván Saavedra; Dante Cáceres

Pharmacogenetics is the study of genetically determined variations in the response to drugs and toxic agents, and their implications on disease. Recently, the discipline has acquired great relevancy due to the development of non-invasive molecular techniques that identify genetic variants in human beings. There is also a need to explain the individual differences in susceptibility to drug actions and disease risk. Genetic variants can modify the magnitude of a pharmacologic effect, toxicity threshold, secondary effects and drug interactions. There are approximately thirty families of drug-metabolizing enzymes with genetic variants that cause functional alterations and variations in pharmacologic activity. We summarize the general knowledge about genetic variants of biotransformation enzymes, their relationship with cancer risk and the role of ethnicity. Cancer pharmacogenetics is another promising and exciting research area that will explain why people with an almost identical group of genes, have a different susceptibility to cancer, whose etiology has genetic and environmental components.


Current Drug Metabolism | 2014

Perception of the Usefulness of Drug/Gene Pairs and Barriers for Pharmacogenomics in Latin America

Luis Quiñones; Maria Alejandra Lavanderos; Juan Cayún; Elena García-Martín; J. A. G. Agúndez; Dante Cáceres; Ángela Roco; Jorge Morales; Luisa Herrera; Gonzalo Encina; Carlos Alberto Isaza; María Redal; Laura Larovere; Nestor Walter Soria; Javier Eslava-Schmalbach; Gilberto Castaneda-Hernandez; Andres Lopez-Cortes; Luiz Alexandre Magno; Marisol Lopez; Miguel Angel Chiurillo; Idania Rodeiro; Dinorah Castro de Guerra; Enrique Teran; Francisco E. Estévez-Carrizo; Ismael Lares-Assef

Pharmacogenetics and Pharmacogenomics areas are currently emerging fields focused to manage pharmacotherapy that may prevent undertreatment while avoiding associated drug toxicity in patients. Large international differences in the awareness and in the use of pharmacogenomic testing are presumed, but not well assessed to date. In the present study we review the awareness of Latin American scientific community about pharmacogenomic testing and the perceived barriers for their clinical application. In order to that, we have compiled information from 9 countries of the region using a structured survey which is compared with surveys previously performed in USA and Spain. The most relevant group of barriers was related to the need for clear guidelines for the use of pharmacogenomics in clinical practice, followed by insufficient awareness about pharmacogenomics among clinicians and the absence of regulatory institutions that facilitate the use of pharmacogenetic tests. The higher ranked pairs were TPMT/thioguanine, TPMT/azathioprine, CYP2C9/warfarin, UGT1A1/irinotecan, CYP2D6/amitriptiline, CYP2C19/citalopram and CYP2D6/clozapine. The lower ranked pairs were SLCO1B1/simvastatin, CYP2D6/metoprolol and GP6D/chloroquine. Compared with USA and Spanish surveys, 25 pairs were of lower importance for Latin American respondents. Only CYP2C19/esomeprazole, CYP2C19/omeprazole, CYP2C19/celecoxib and G6PD/dapsone were ranked higher or similarly to the USA and Spanish surveys. Integration of pharmacogenomics in clinical practice needs training of healthcare professionals and citizens, but in addition legal and regulatory guidelines and safeguards will be needed. We propose that the approach offered by pharmacogenomics should be incorporated into the decision-making plans in Latin America.


Indoor and Built Environment | 1997

Influence of Atmospheric Air Pollution on Indoor Air Quality: Comparison of Chemical Pollutants and Mutagenicity Levels in Santiago (Chile):

Lionel Gil; Dante Cáceres; Marta Adonis

The influence of atmospheric pollution on indoor air quality (IAQ) was studied in downtown Santiago (Chile). Carbon monoxide (CO), nicotine, the mass of respirable particulate matter below 5 μm (PM5 fraction) and total and carcinogenic polycyclic aromatic hydrocarbons (PAHs) were simultaneously monitored indoors and outdoors in restaurants, offices and oth er places. The levels of CO changed simultaneously outdoors and indoors (r = 0.89), especially during traffic rush hours, masking the contribution of other indoor sources and showing the importance of infiltration of outdoor air indoors. CO concentrations ranged from 1.0 to 73 ppm and 0.5 to 93 ppm for indoors and outdoors, respectively. The highest running 8-hour average levels measured were 16 and 18 ppm, respectively. These levels exceeded the Chilean 8-hour standard of 9 ppm to the extent of 178% indoors and by more than 200% outdoors. PM5 concentrations were high and showed no significant differences (p > 0.05) between indoors and outdoors: levels in restaurants, offices and other places were not significantly different from each other. The concentrations of total and carcinogenic PAHs were also high indoors and outdoors, outdoor levels being higher than those indoors although no significant differences (p > 0.05) in indoor levels were found between restaurants and offices and between offices and other places. Nicotine levels showed significant differences (p < 0.05) between indoor and outdoor levels. In addition, great differences (p < 0.05) in indoor levels were also found between offices and restaurants, and offices and other places. Mutagenic response in Salmonella typhimurium by organic extracts from PM 5 collected in downtown Santiago in Bandera street and in a rural area showed that the extracts from the Santiago samples are highly mutagenic. These results suggest that in downtown Santiago, infiltration might be the main source of indoor pollution. Symptoms and health effects probably related to air pollution in people working in Bandera street and in Curacavi, a rural area located 45 km from Santiago were surveyed. This showed clearly that people working in downtown Santiago have greater frequency of eye complaints, sneezing attacks, cough, throat dryness and rhinitis.

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Rafael A. Burgos

Austral University of Chile

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