Gerardo Enrique Muñoz-Maldonado

Prof. Dr. Gerardo Enrique Muñoz-Maldonado

orcid

Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

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

Representative Publications

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1 November 2011 in Cytotherapy
Verified
Journal Article
Closed access
GMGerardo Enrique Muñoz-Maldonado
Gerardo Enrique Muñoz-Maldonado
CPCarlos Alberto Alvarez Pérez
Carlos Alberto Alvarez Pérez
ECEli Esaú Aguiñaga Covarrubias
Eli Esaú Aguiñaga Covarrubias
SCSylvia Aide Martínez Cabriales
Sylvia Aide Martínez Cabriales
LLLaura Alvarado Leyva
Laura Alvarado Leyva
DADavid Gómez Almaguer
David Gómez Almaguer

1 January 2017 in Molecular Medicine
Verified
Journal Article
Open access
SSSandra K. Santuario-Facio
Sandra K. Santuario-Facio
SCServando Cardona-Huerta
Servando Cardona-Huerta
YPYadira X. Perez-Paramo
Yadira X. Perez-Paramo
VICTOR TREVINOVICTOR TREVINO
VICTOR TREVINO
FHFrancisco Hernandez-Cabrera
Francisco Hernandez-Cabrera
RORocio Ortiz-Lopez
Rocio Ortiz-Lopez
Triple-negative breast cancer (TNBC) is an aggressive subtype of breast cancer tumors. Comparisons between TNBC and non-triple negative breast cancer (nTNBC) may help to differentiate key components involved in TNBC neoplasms. The purpose of the study was to analyze the expression profile of TNBC versus nTNBC tumors in a homogeneous population from northeastern Mexico. A prospective study of 50 patients was conducted (25 TNBC and 25 nTNBC). Clinic parameters were equally distributed for TNBC and nTNBC: age at diagnosis (51 vs 47 years, p=0.1), glucose levels (107 mg/dl vs 104 mg/dl, p=0.64), and body mass index (28 vs 29, p=0.14), respectively. Core biopsies were collected for histopathological diagnosis and gene expression analyses. Total RNA was isolated and expression profiling was performed. 40 genes showed differential expression pattern in TNBC tumors. Among these, 9 over-expressed genes (PRKX/PRKY, UGT8, HMGA1, LPIN1, HAPLN3, and ANKRD11), and one under-expressed (ANX9) gene are involved in general metabolism. Based on this biochemical peculiarity, and the over-expression of BCL11A and FOXC1 (involved in tumor growth and metastasis, respectively) we validated by qPCR the expression profile of 7 genes out of the signature. In this report, a new gene signature for TNBC is proposed. To our knowledge, this is the first TNBC signature which describes genes involved in general metabolism. The findings may be pertinent for Mexican patients and require to be evaluated in further ethnic groups and populations.

1 May 2017
Verified
Journal Article
Open access
FRF. Reyna-Sepúlveda
F. Reyna-Sepúlveda
APA. Ponce-Escobedo
A. Ponce-Escobedo
AGA. Guevara-Charles
A. Guevara-Charles
MEM. Escobedo-Villarreal
M. Escobedo-Villarreal
EPE. Pérez-Rodríguez
E. Pérez-Rodríguez
MHM. Hernández-Guedea
M. Hernández-Guedea
Kidney transplantation is the most cost-effective therapy for end-stage renal disease. Post-operative complications account for 15%–17% of all cases and are associated with significant morbidity. Currently 4.8% of post-transplantation patients have returned to dialysis. Our center’s main transplant origin is cadaveric donation. To review surgical complications of kidney transplantation over the past 5 years. This was an observational descriptive study that included all patients from 2011 to 2015. A total of 55 cases were reviewed. Diabetic nephropathy was the etiology in 30.9% of cases. Post-surgical complications occurred in 12.7% of patients with a post-operative mortality of 4%. Graft survival at 1 year was 82.4% with a 91% 1-year patient survival. Early identification and treatment of surgical complications are critical for patient and graft survival. Complications are low but significant.

23 January 2017 in Oncology Letters
Verified
Journal Article
Open access
PDF file
JPJose J. Perez-Trujillo
Jose J. Perez-Trujillo
RGRodolfo Garza-Morales
Rodolfo Garza-Morales
JBJose A. Barron-Cantu
Jose A. Barron-Cantu
GFGabriel Figueroa-Parra
Gabriel Figueroa-Parra
AGAracely Garcia-Garcia
Aracely Garcia-Garcia
MLMaria Loera-Arias
Maria Loera-Arias
Cellular immune responses play a critical role in the eradication of intracellular infections and malignant cells through the recognition and subsequent removal of the infection or malignant cells. Effective antigen presentation is crucial for stimulating the immune system against malignant cells. Calreticulin (CRT) has been used to improve antigen presentation. However, CRT overexpression has been previously associated with the development of pancreatic and breast cancer. The import and retention signals of CRT in the endoplasmic reticulum (ER) can be used to overcome CRT overexpression. The present study describes the potent antitumor effect of a DNA vaccine encoding human papillomavirus type 16 E6 and E7 antigens flanked by ER import and retention signals (SP‑E6E7m‑KDEL). The effect of this vaccine was compared with that of E6 and E7 antigens fused to human full‑length CRT (hCRT‑E6E7m). In the present study, the effectiveness of SP‑E6E7m‑KDEL for inducing an interferon‑γ antigen‑specific, response and its therapeutic effect against tumors was demonstrated, which was as effective as immunization against those antigens fused to CRT. This simplified strategy, using ER import and retention signal peptides to direct antigens to this organelle, provides an efficient alternative to traditional vaccines and, more importantly, a safe and potent system to induce a therapeutic antitumor response.

29 January 2019 in Oncology Letters
Verified
Journal Article
Closed access
PDF file
GUGrecia I. Uscanga‑Perales
Grecia I. Uscanga‑Perales
SSSandra K. Santuario‑Facio
Sandra K. Santuario‑Facio
Celia N Sánchez-DomínguezCelia N Sánchez-Domínguez
Celia N Sánchez-Domínguez
SCServando Cardona‑Huerta
Servando Cardona‑Huerta
PRPablo Ruiz-Flores
Pablo Ruiz-Flores
GMGerardo Enrique Muñoz-Maldonado
Gerardo Enrique Muñoz-Maldonado
Triple negative breast cancer (TNBC) is a subtype of breast cancer of heterogeneous nature that is negative for estrogen receptor (ER), progesterone receptor (PR) and growth factor human epidermal 2 (HER2) following immunohistochemical analysis. TNBC is frequently characterized by relapse and reduced survival. To date, there is no targeted therapy for this type of cancer. Chemotherapy, radiotherapy, and surgery remain as the standard treatments options. The lack of a target therapy and the heterogeneity of TNBC highlight the need to seek new therapeutic options. In this study, fresh tissue samples of TNBC were analyzed with a panel of 48 driver genes (212 amplicons) that are likely to be therapeutic targets. We found intron variants, missense, stop gained and splicing variants in TP53, PIK3CA and FLT3 genes. Interestingly, all the analyzed samples had at least two variants in the TP53 gene, one being a drug response variant, rs1042522, found in 94% of our samples. We also found seven additional variants not previously reported in the TP53 gene, to the best of our knowledge, with probable deleterious characteristics of the tumor suppressor gene. We found four genetic variants in the PIK3CA gene, including two missense variants. The rs2491231 variant in the FLT3 gene was identified in 84% (16/19) of the samples, which not yet reported for TNBC, to the best of our knowledge. In conclusion, genetic variants in TP53 were found in all TNBC tumors, with rs1042522 being the most frequent (94% of TNBC biopsies), which had not been previously reported in TNBC. Also, we found two missense variants in the PIK3CA gene. These results justify the validation of these genetic variants in a large cohort, as well as the extensive study of their impact on the prognosis and therapy management of TBNC.

5 February 2019 in Cirugía y Cirujanos
Verified
Journal Article
Closed access
FRFrancisco Reyna-Sepúlveda
Francisco Reyna-Sepúlveda
GMGerardo Enrique Muñoz-Maldonado
Gerardo Enrique Muñoz-Maldonado
EPEdelmiro Pérez-Rodríguez
Edelmiro Pérez-Rodríguez
FHFabiola Hernández-Trejo
Fabiola Hernández-Trejo
AGAsdrúbal Guevara-Charles
Asdrúbal Guevara-Charles
MHMarco A. Hernández-Guedea
Marco A. Hernández-Guedea
Periampullary neoplasms account for over 30,000 cancer-related deaths per year in the United States. Pancreaticoduodenectomy (PD) is considered the surgical standard and is the only curative treatment option for these pathologies. The objective of this study was to report the prognostic factors in survival and surgical complications in PD. A total of 178 cases are reported, several variables were reviewed and the same surgical technique was used by the same surgeon. A total of 151 PD were reviewed. The most common initial symptoms were jaundice, 111 (73%), abdominal pain, 20 (13%), and oral intolerance, 10 (6%). Poor prognostic factors for survival were the presence of a previous pathology, days of hospitalization, positive margins, and weight loss. With the experience gained, a decrease in surgical time, intraoperative bleeding, and transfusions performed was achieved. Our complication rate remained at 20%, lower than that reported in literature. PD is the only option of cure for patients with pancreatic and periampullary tumors. This procedure has been linked to high morbidity and mortality even in high-volume centers. A pancreatic fistula is the most feared complication; therefore, multiple pancreatojejunostomy techniques have been described in literature. It is important to continue reporting these cases to reach a consensus on this technique.