Jennyfer M García-Cárdenas

Ms. Jennyfer M García-Cárdenas

orcid

Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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21 November 2018 in BioMed Research International
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CSCarolina Salazar-Ruales
Carolina Salazar-Ruales
JAJessica-Viviana Arguello
Jessica-Viviana Arguello
Andrés López-CortésAndrés López-Cortés
Andrés López-Cortés
Alejandro Cabrera-AndradeAlejandro Cabrera-Andrade
Alejandro Cabrera-Andrade
JGJennyfer M García-Cárdenas
Jennyfer M García-Cárdenas
CPCesar Paz-y-Mino
Cesar Paz-y-Mino
Head and neck squamous cell carcinoma (HNSCC) is the sixth most common cancer with the highest incidence worldwide. HNSCC is often diagnosed at advanced stages, incurring significant high mortality and morbidity. The use of saliva, as a noninvasive tool for the diagnosis of cancer, has recently increased. Salivary microRNAs (miRNAs) have emerged as a promising molecular tool for early diagnosis of HNSCC. The aim was to identify the differential expression of salivary miRNAs associated with HNSCC in the high altitude mestizo Ecuadorian population. Using PCR Arrays, miR-122-5p, miR-92a-3p, miR-124-3p, miR-205-5p, and miR-146a-5p were found as the most representative ones. Subsequently, miRNAs expression was confirmed in saliva samples from 108 cases and 108 controls. miR-122-5p, miR-92a-3p, miR-124-3p, and miR-146a-5p showed significant statistical difference between cases and controls with areas under the curve (AUC) of 0.73 (p < 0.001), 0.70 (p < 0.001), 0.71 (p = 0.002), and 0.66 (p = 0.008), respectively. miRNAs were also deregulated in between HNSCC localizations. A differentiated expression of miR-122-5p between oral cancer and oropharynx cancer (AUC of 0.96 p = 0.01) was found: miR-124-3p between larynx and pharynx (AUC = 0.97, p < 0.01) and miR-146a-5p between larynx, oropharynx, and oral cavity (AUC = 0.96, p = 0.01). Moreover, miR-122-5p, miR-124-3p, miR-205-5p, and miR-146a-5p could differentiate between HPV+ and HPV- (p=0.004). Finally, the expression profiles of the five miRNAs were evaluated to discriminate HNSCC patient’s tumor stages (TNM 2-4). miR-122-5p differentiates TNM 2 and 3 (p = 0.002, AUC = 0.92), miR-124-3p TNM 2, 3, and 4 (p < 0.001, AUC = 98), miR-146a-5p TNM 2 and 3 (p < 0.001, AUC = 0.97), and miR-92a-3p TNM 3 (p < 0.001, AUC = 0.99). Taken together, these findings show that altered expression of miRNAs could be used as biomarkers for HNSCC diagnosis in the high altitude mestizo Ecuadorian population.

25 June 2019 in Scientific Reports
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AZAna Karina Zambrano
Ana Karina Zambrano
AGAníbal Gaviria
Aníbal Gaviria
SCSantiago Cobos-Navarrete
Santiago Cobos-Navarrete
CGCarmen Gruezo
Carmen Gruezo
CRCristina Jeanneth Rodríguez-Pólit
Cristina Jeanneth Rodríguez-Pólit
CPCesar Paz-y-Mino
Cesar Paz-y-Mino
The history of Ecuador was marked by the arrival of Europeans with Africans, resulting in the mixture of Native Americans with Africans and Europeans. The present study contributes to the knowledge of the Ecuadorian mestizo population by offering information about ancestry and ethnic heterogeneity. Forty-six AIM-InDels (Ancestry Informative Insertion/Deletion Markers) were used to obtain information on 240 Ecuadorian individuals from three regions (Amazonia, the Highlands, and the Coast). As a result, the population involved a significant contribution from Native Americans (values up to 51%), followed by Europeans (values up to 33%) and Africans (values up to 13%). Furthermore, we compared the data obtained with nine previously reported scientific articles on autosomal, mitochondrial DNA and Y chromosomes. The admixture results correspond to Ecuador’s historical background and vary slightly between regions.

7 August 2019 in Frontiers in Molecular Biosciences
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Journal Article
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JGJennyfer M García-Cárdenas
Jennyfer M García-Cárdenas
SGSantiago Guerrero
Santiago Guerrero
Andrés López-CortésAndrés López-Cortés
Andrés López-Cortés
Isaac Armendáriz-CastilloIsaac Armendáriz-Castillo
Isaac Armendáriz-Castillo
PGPatricia Guevara-Ramírez
Patricia Guevara-Ramírez
CPCesar Paz-y-Mino
Cesar Paz-y-Mino
Colorectal cancer (CRC) is a major health problem with an estimated 1. 8 million new cases worldwide. To date, most CRC studies have focused on DNA-related aberrations, leaving post-transcriptional processes under-studied. However, post-transcriptional alterations have been shown to play a significant part in the maintenance of cancer features. RNA binding proteins (RBPs) are uprising as critical regulators of every cancer hallmark, yet little is known regarding the underlying mechanisms and key downstream oncogenic targets. Currently, more than a thousand RBPs have been discovered in humans and only a few have been implicated in the carcinogenic process and even much less in CRC. Identification of cancer-related RBPs is of great interest to better understand CRC biology and potentially unveil new targets for cancer therapy and prognostic biomarkers. In this work, we reviewed all RBPs which have a role in CRC, including their control by microRNAs, xenograft studies and their clinical implications.

15 October 2019 in The Pharmacogenomics Journal
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Andrés López-CortésAndrés López-Cortés
Andrés López-Cortés
CPCesar Paz-y-Mino
Cesar Paz-y-Mino
SGSantiago Guerrero
Santiago Guerrero
GJGABRIELA Jaramillo-Koupermann
GABRIELA Jaramillo-Koupermann
ÁCÁngela León Cáceres
Ángela León Cáceres
NSNéstor W. Soria
Néstor W. Soria

1 October 2015 in The American Journal of the Medical Sciences
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CPCesar Paz-y-Mino
Cesar Paz-y-Mino
JGJennyfer M García-Cárdenas
Jennyfer M García-Cárdenas
Andrés López-CortésAndrés López-Cortés
Andrés López-Cortés
CSCarolina Salazar
Carolina Salazar
PLPaola E. Leone
Paola E. Leone
MSMarcos Serrano
Marcos Serrano

23 December 2019 in BioMed Research International
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Journal Article
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Isaac Armendáriz-CastilloIsaac Armendáriz-Castillo
Isaac Armendáriz-Castillo
SGSantiago Guerrero
Santiago Guerrero
AVAntonella Vera-Guapi
Antonella Vera-Guapi
TCTiffany Cevallos-Vilatuña
Tiffany Cevallos-Vilatuña
JGJennyfer M García-Cárdenas
Jennyfer M García-Cárdenas
CPCesar Paz-y-Mino
Cesar Paz-y-Mino
Background. Many studies, comparing the health associated risks of electronic cigarettes with conventional cigarettes focus mainly on the common chemical compounds found between them. Aim. Review chemical compounds found exclusively in electronic cigarettes and describe their toxic effects, focusing on electronic-cigarette-only and dual electronic-cigarette and conventional cigarette users. Data Sources. Literature search was carried out using PubMed. Study Eligibility Criteria. Articles related exclusively to conventional and electronic cigarettes’ chemical composition. Articles which reported to be financed from tobacco or electronic cigarettes industries, not reporting source of funding, not related to the chemical composition of electronic and conventional cigarettes and not relevant to tobacco research were excluded. Methods and Results. Chemical compounds reported in the selected studies were tabulated using the Chemical Abstracts Service registry number for chemical substances information. A total of 50 chemical compounds were exclusively reported to be present in electronic cigarettes. Crucial health risks identified were: eye, skin, and respiratory tract irritation, with almost 50% of incidence, an increment of 10% in cytotoxic effects, when compared to compounds in common with conventional cigarettes and around 11% of compounds with unknown effects to human health. Limitations. Articles reporting conflicts of interest. Conclusions and Implications of Key Findings. Despite being considered as less harmful for human health, compounds found in electronic cigarettes are still a matter of research and their effects on health are yet unknown. The use of these devices is not recommended for first time users and it is considered hazardous for dual users.