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Item type:Publication, Genotyping the High Altitude Mestizo Ecuadorian Population Affected with Prostate Cancer(Hindawi Limited, 2017) ;Andrés López-Cortés ;Alejandro Cabrera-Andrade ;Carolina Salazar-Ruales; Santiago Guerrero<jats:p>Prostate cancer (PC) is the second most commonly diagnosed type of cancer in males with 1,114,072 new cases in 2015. The MTHFR enzyme acts in the folate metabolism, which is essential in methylation and synthesis of nucleic acids. MTHFR C677T alters homocysteine levels and folate assimilation associated with DNA damage. Androgens play essential roles in prostate growth. The SRD5A2 enzyme metabolizes testosterone and the V89L polymorphism reduces in vivo SRD5A2 activity. The androgen receptor gene codes for a three-domain protein that contains two polymorphic trinucleotide repeats (CAG, GGC). Therefore, it is essential to know how PC risk is associated with clinical features and polymorphisms in high altitude Ecuadorian mestizo populations. We analyzed 480 healthy and 326 affected men from our three retrospective case-control studies. We found significant association between MTHFR C/T (odds ratio [OR] = 2.2;<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M1"><mml:mi>P</mml:mi><mml:mo>=</mml:mo><mml:mn fontstyle="italic">0.009</mml:mn></mml:math>), MTHFR C/T+T/T (OR = 2.22;<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M2"><mml:mi>P</mml:mi><mml:mo>=</mml:mo><mml:mn fontstyle="italic">0.009</mml:mn></mml:math>), and PC. The SRD5A2 A49T substitution was associated with higher pTNM stage (OR = 2.88;<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M3"><mml:mi>P</mml:mi><mml:mo>=</mml:mo><mml:mn fontstyle="italic">0.039</mml:mn></mml:math>) and elevated Gleason grade (OR = 3.15;<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M4"><mml:mi>P</mml:mi><mml:mo>=</mml:mo><mml:mn fontstyle="italic">0.004</mml:mn></mml:math>). Additionally, patients with ≤21 CAG repeats have an increased risk of developing PC (OR = 2.99;<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M5"><mml:mi>P</mml:mi><mml:mo><</mml:mo><mml:mn fontstyle="italic">0.001</mml:mn></mml:math>). In conclusion, genotype polymorphism studies are important to characterize genetic variations in high altitude mestizo populations.</jats:p> - Some of the metrics are blocked by yourconsent settings
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Item type:Publication, Ancestry study in Ecuadorian population with multiple myeloma(Ovid Technologies (Wolters Kluwer Health), 2017) ;P.E. Leone ;A. Cabrera-Andrade ;J.M. García-Cárdenas ;D.A. González - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Mutation rates for 29 short tandem repeat loci from the Ecuadorian population(Elsevier BV, 2017-12) ;A. Gaviria ;M. Vela ;G. Fiallos ;C. GruezoS. Cobos - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Genetic characterization of four Colombian populations using Investigator® Argus X-12 kit(Elsevier BV, 2017-12) ;J.J. Builes ;L. Mendoza ;A. Gaviria; N.D. Suarez - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Genetic data for twenty-two autosomal STRs (PowerPlex® Fusion) from Afro-Ecuadorian population(Elsevier BV, 2017-12) ;A. Gaviria ;M. Vela ;G. Fiallos ;C. GruezoS. Cobos - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Molecular analysis of ancestry informative markers (AIMs-INDELs) in a high altitude Ecuadorian mestizo population affected with breast cancer(Elsevier BV, 2017-12) ;A. López-Cortés ;G. Echeverría-Garcés ;G. Burgos; A. Cabrera-Andrade - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Evaluation of ancestral membership proportions and genotype distribution in the perception of Umami taste in Ecuadorian mestizos(Elsevier BV, 2017-12); ;J.M. García-Cárdenas ;A. López-Cortés ;A. Cabrera-Andrade - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Analysis of Racial/Ethnic Representation in Select Basic and Applied Cancer Research Studies(Springer Science and Business Media LLC, 2018-09-18) ;Santiago Guerrero ;Andrés López-Cortés ;Alberto Indacochea ;Jennyfer M. García-Cárdenas<jats:title>Abstract</jats:title><jats:p>Over the past decades, consistent studies have shown that race/ethnicity have a great impact on cancer incidence, survival, drug response, molecular pathways and epigenetics. Despite the influence of race/ethnicity in cancer outcomes and its impact in health care quality, a comprehensive understanding of racial/ethnic inclusion in oncological research has never been addressed. We therefore explored the racial/ethnic composition of samples/individuals included in fundamental (patient-derived oncological models, biobanks and genomics) and applied cancer research studies (clinical trials). Regarding patient-derived oncological models (n = 794), 48.3% have no records on their donor’s race/ethnicity, the rest were isolated from White (37.5%), Asian (10%), African American (3.8%) and Hispanic (0.4%) donors. Biobanks (n = 8,293) hold specimens from unknown (24.56%), White (59.03%), African American (11.05%), Asian (4.12%) and other individuals (1.24%). Genomic projects (n = 6,765,447) include samples from unknown (0.6%), White (91.1%), Asian (5.6%), African American (1.7%), Hispanic (0.5%) and other populations (0.5%). Concerning clinical trials (n = 89,212), no racial/ethnic registries were found in 66.95% of participants, and records were mainly obtained from Whites (25.94%), Asians (4.97%), African Americans (1.08%), Hispanics (0.16%) and other minorities (0.9%). Thus, two tendencies were observed across oncological studies: lack of racial/ethnic information and overrepresentation of Caucasian/White samples/individuals. These results clearly indicate a need to diversify oncological studies to other populations along with novel strategies to enhanced race/ethnicity data recording and reporting.</jats:p> - Some of the metrics are blocked by yourconsent settings
Item type:Publication, The geographic mosaic of Ecuadorian Y-chromosome ancestry(Elsevier BV, 2018-03) ;U. Toscanini ;A. Gaviria ;J. Pardo-Seco ;A. Gómez-CarballaF. Moscoso
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