Alejandro González Vidal

Dr. Alejandro González Vidal

orcid

Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

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

Representative Publications

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7 March 2022 in International Journal of Radiation Biology
Verified
Journal Article
Closed access
JAJuan Carlos Alamilla
Juan Carlos Alamilla
ABAntonio M. Burgos-Molina
Antonio M. Burgos-Molina
AVAlejandro González Vidal
Alejandro González Vidal
Francisco Sendra-PorteroFrancisco Sendra-Portero
Francisco Sendra-Portero
MRMiguel J. Ruiz-Gómez
Miguel J. Ruiz-Gómez
The aim of this work is to review the published studies on radiation resistance mechanisms and molecular markers involved in different tumors. The revision has been focused in the last 5 years (201...

30 August 2023 in Antioxidants
Verified
Journal Article
Open access
PDF file
AVAlejandro González Vidal
Alejandro González Vidal
SMSilvia Mercado-Sáenz
Silvia Mercado-Sáenz
ABAntonio M. Burgos-Molina
Antonio M. Burgos-Molina
JAJuan Carlos Alamilla
Juan Carlos Alamilla
Miguel AlcarazMiguel Alcaraz
Miguel Alcaraz
MRMiguel J. Ruiz-Gómez
Miguel J. Ruiz-Gómez
The repair of the damage produced to the genome and proteome by the action of ionizing radiation, oxidizing agents, and during aging is important to maintain cellular homeostasis. Many of the metabolic pathways influence multiple processes. In this way, this work aims to study the relationship between resistance/response to ionizing radiation, cellular aging, and the response mechanisms to oxidative stress, free radicals, reactive oxygen species (ROS), and antioxidant activity in the yeast S. cerevisiae. Systems biology allows us to use tools that reveal the molecular mechanisms common to different cellular response phenomena. The results found indicate that homologous recombination, non-homologous end joining, and base excision repair pathways are the most important common processes necessary to maintain cellular homeostasis. The metabolic routes of longevity regulation are those that jointly contribute to the three phenomena studied. This study proposes eleven common biomarkers for response/resistance to ionizing radiation and aging (EXO1, MEC1, MRE11, RAD27, RAD50, RAD51, RAD52, RAD55, RAD9, SGS1, YKU70) and two biomarkers for response/resistance to radiation and oxidative stress, free radicals, ROS, and antioxidant activity (NTG1, OGG1). In addition, it is important to highlight that the HSP104 protein could be a good biomarker common to the three phenomena studied.

2 April 2021 in International Journal of Environmental Health Research
Verified
Journal Article
Closed access
SMSilvia Mercado-Sáenz
Silvia Mercado-Sáenz
BLBeatriz López-Díaz
Beatriz López-Díaz
ABAntonio M. Burgos-Molina
Antonio M. Burgos-Molina
Francisco Sendra-PorteroFrancisco Sendra-Portero
Francisco Sendra-Portero
AVAlejandro González Vidal
Alejandro González Vidal
MRMiguel J. Ruiz-Gómez
Miguel J. Ruiz-Gómez
This study evaluates the DNA damage induced by pulsed magnetic field (MF) on S. cerevisiae cells exposed during chronological aging. Samples were exposed to 25 Hz pulsed MF (1.5mT, 8 h/day) while cells were aging chronologically. Clonogenic drop test was used to study cellular survival and the mutation frequency was evaluated by scoring the spontaneous revertant mutants. DNA damage analysis was performed after aging by electrophoresis and image analysis. Yeast cells aged during 40 days of exposure showing that pulsed MF exposure induced a premature aging. In addition, a gradual increase in spontaneous mutants was found in pulsed MF samples in relation to unexposed controls. An increase in DNA degradation, over the background level in relation to controls, was observed at the end of the exposure period. In conclusion, exposure of S. cerevisiae cells to pulsed MF during chronological aging could induce genomic DNA damage.

22 June 2025 in Applied Sciences
Verified
Journal Article
Open access
PDF file
VGVicente M. García-Cañizares
Vicente M. García-Cañizares
AVAlejandro González Vidal
Alejandro González Vidal
ABAntonio M. Burgos-Molina
Antonio M. Burgos-Molina
SMSilvia Mercado-Sáenz
Silvia Mercado-Sáenz
Francisco Sendra-PorteroFrancisco Sendra-Portero
Francisco Sendra-Portero
MRMiguel J. Ruiz-Gómez
Miguel J. Ruiz-Gómez
Breast, colon, and ovarian cancers are among the most prevalent malignancies worldwide, with distinct clinical features. This study aims to identify key proteins as common biomarkers for breast, colon, and ovarian cancer through protein analysis, molecular mechanisms, and patient sample validation. Data mining from curated databases identified 483 proteins for breast cancer, 521 for colon cancer, and 223 for ovarian cancer. Interaction network analysis revealed shared clusters involved in cancer progression, DNA repair, and cell proliferation. A core set of 27 proteins was found to be common across all three cancer types, participating in key biological processes such as DNA damage response, cell proliferation, and apoptosis. Notably, these proteins are implicated in KEGG pathways linked to multiple cancers. Differential gene expression analysis revealed significant alterations in the expressions of MSH2 and KIT across the three cancers, suggesting their potential as common biomarkers. The high expression of these proteins was associated with better survival outcomes, highlighting their potential as common biomarkers for breast, colon, and ovarian cancers. The in-silico methodology integrated various bioinformatic tools—including cluster identification, gene expression profiling, protein network visualization, and biomarker prediction—enhancing the understanding of shared molecular mechanisms and potential therapeutic targets.

2 September 2021 in International Journal of Environmental Health Research
Verified
Journal Article
Closed access
AVAlejandro González Vidal
Alejandro González Vidal
SMSilvia Mercado-Sáenz
Silvia Mercado-Sáenz
ABAntonio M. Burgos-Molina
Antonio M. Burgos-Molina
Francisco Sendra-PorteroFrancisco Sendra-Portero
Francisco Sendra-Portero
MRMiguel J. Ruiz-Gómez
Miguel J. Ruiz-Gómez
The response of plants to magnetic fields (MF) is not fully understood. This work studies the effects of pulsed MF on the germination and growth of Allium cepa roots. Onions were exposed to 25Hz, 1.5mT, 33h. Pulsed MF was generated by a Helmholtz-type equipment that generated rectangular voltage pulses. The results showed that fewer roots grew in the specimens exposed to pulsed MF (14±6 roots on day 1 to 21±8 on day 4) than in the control groups (32±17 to 48±23) (p<0.05 Friedman). Control specimens showed a root mean length of 7±4 mm (day 1) and 24±10 mm (day 4). The specimens treated with pulsed MF showed a length of 4±2 mm (day 1), reaching 18±9 mm on day 4 (p<0.001 ANOVA). In conclusion, the exposure of Allium cepa specimens to 25Hz, 1.5mT pulsed MF during 33h produces a decrease in the germination and growth of roots.

15 September 2022 in International Journal of Radiation Biology
Verified
Journal Article
Closed access
BLBeatriz López-Díaz
Beatriz López-Díaz
SMSilvia Mercado-Sáenz
Silvia Mercado-Sáenz
ABAntonio M. Burgos-Molina
Antonio M. Burgos-Molina
AVAlejandro González Vidal
Alejandro González Vidal
Francisco Sendra-PorteroFrancisco Sendra-Portero
Francisco Sendra-Portero
MRMiguel J. Ruiz-Gómez
Miguel J. Ruiz-Gómez
Many articles describe the effects of extremely low-frequency magnetic fields (MFs) on DNA damage induction. However, the mechanism of MF interaction with living matter is not yet known with certai...