Rhonda F. Souza

ORCID: 0000-0003-3484-2807
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About
Contact & Profiles
Research Areas
  • Esophageal Cancer Research and Treatment
  • Eosinophilic Esophagitis
  • Esophageal and GI Pathology
  • Helicobacter pylori-related gastroenterology studies
  • Gastroesophageal reflux and treatments
  • Gastric Cancer Management and Outcomes
  • Cancer-related gene regulation
  • Eosinophilic Disorders and Syndromes
  • Genetic factors in colorectal cancer
  • Wnt/β-catenin signaling in development and cancer
  • IL-33, ST2, and ILC Pathways
  • Epigenetics and DNA Methylation
  • Cytokine Signaling Pathways and Interactions
  • Cancer Cells and Metastasis
  • Inflammatory mediators and NSAID effects
  • RNA modifications and cancer
  • Digestive system and related health
  • Inflammatory Bowel Disease
  • Dysphagia Assessment and Management
  • Lung Cancer Treatments and Mutations
  • Colorectal Cancer Treatments and Studies
  • Tracheal and airway disorders
  • Cardiovascular Disease and Adiposity
  • Gastrointestinal Tumor Research and Treatment
  • NF-κB Signaling Pathways

Baylor University Medical Center
2012-2025

Baylor Medical Center at Garland
2017-2025

Baylor Scott & White Health
2021-2025

The University of Texas at Arlington
2024

Texas A&M Health Science Center
2024

Veterans Health Administration
2004-2023

VA North Texas Health Care System
2009-2019

RELX Group (Netherlands)
2018

The University of Texas Health Science Center at Houston
2018

Rhode Island Hospital
2018

By expressing two genes (hTERT and Cdk4), we have developed a method to reproducibly generate continuously replicating human bronchial epithelial cell (HBEC) lines that provide novel resource study the molecular pathogenesis of lung cancer differentiation cells. Twelve biopsy specimens obtained from persons with without were placed into short-term culture serially transfected retroviral constructs containing cyclin-dependent kinase (Cdk) 4 telomerase reverse transcriptase (hTERT), resulting...

10.1158/0008-5472.can-04-3703 article EN Cancer Research 2004-12-15

<h3>Objective</h3> Eosinophilic oesophagitis (EoE) and gastro-oesophageal reflux disease (GORD) can have similar clinical histological features. Proton pump inhibitors (PPIs) are used to distinguish the disorders, with assumption that only GORD respond PPIs. Oesophageal expression of eotaxin-3 stimulated by Th2 cytokines might contribute oesophageal eosinophilia in EoE. cytokine effects on oesophagus not known. The objective authors was explore molecular mechanisms squamous cells from...

10.1136/gutjnl-2012-302250 article EN Gut 2012-05-12

Barrett's esophagus (BE) is a common condition associated with chronic gastroesophageal reflux disease. BE the only known precursor to esophageal adenocarcinoma, highly lethal cancer an increasing incidence over last 5 decades. These revised guidelines implement Grading of Recommendations, Assessment, Development, and Evaluation methodology propose recommendations for definition diagnosis BE, screening surveillance patients medical endoscopic treatment its early neoplasia. Important changes...

10.14309/ajg.0000000000001680 article EN The American Journal of Gastroenterology 2022-03-31

Background Patients who have esophageal eosinophilia without gastroesophageal reflux disease (GERD) nevertheless can respond to proton pump inhibitors (PPIs), which anti-inflammatory actions independent of effects on gastric acid secretion. In cell cultures, omeprazole has been reported inhibit Th2 cytokine-stimulated expression eotaxin-3, an eosinophil chemoattractant contributing in eosinophilic esophagitis (EoE). The objective this study was elucidate molecular mechanisms underlying PPI...

10.1371/journal.pone.0050037 article EN cc-by PLoS ONE 2012-11-21

The histologic changes associated with acute gastroesophageal reflux disease (GERD) have not been studied prospectively in humans. Recent studies animals challenged the traditional notion that esophagitis develops when esophageal surface epithelial cells are exposed to lethal chemical injury from refluxed acid.To evaluate features of inflammation GERD study its pathogenesis.Patients Dallas Veterans Affairs Medical Center who had successfully treated proton pump inhibitors (PPIs) began...

10.1001/jama.2016.5657 article EN JAMA 2016-05-17

Heartburn that persists despite proton-pump inhibitor (PPI) treatment is a frequent clinical problem with multiple potential causes. Treatments for PPI-refractory heartburn are of unproven efficacy and focus on controlling gastroesophageal reflux reflux-reducing medication (e.g., baclofen) or antireflux surgery dampening visceral hypersensitivity neuromodulators desipramine).

10.1056/nejmoa1811424 article EN New England Journal of Medicine 2019-10-16
Evan S. Dellon Nirmala Gonsalves J. Pablo Abonia Jeffrey A. Alexander Nicoleta C. Arva and 86 more Dan Atkins Stephen Attwood Marcus Auth Dominique D. Bailey Luc Biederman Carine Blanchard Peter A Bonis Paroma Bose Albert J. Bredenoord Joy W. Chang Mirna Chehade Margaret H. Collins Carlo Di Lorenzo Jorge Amil Dias Ranjan Dohil Christophe Dupont Gary W. Falk Cristina Targa Ferreira Adam Fox Robert M. Genta Thomas Greuter Sandeep K. Gupta Ikuo Hirano Girish Hiremath Jennifer L. Horsley‐Silva Shunji Ishihara Norihisa Ishimura Elizabeth T. Jensen Carolina Gutiérrez‐Junquera David A. Katzka Paneez Khoury Yoshikazu Kinoshita Kara Kliewer Sibylle Koletzko John Leung Chris A. Liacouras Alfredo J. Lucendo Lisa J. Martin Emily C. McGowan Calies Menard‐Katcher David C. Metz Talya L. Miller Fouad J. Moawad Amanda B. Muir Vincent A. Mukkada Simon Murch Quan M. Nhu Ichiro Nomura Samuel Nurko Yoshikazu Ohtsuka Salvatore Oliva Rok Orel Alexandra Papadopoulou Dhyanesh A. Patel Robert D. Pesek Kathryn A. Peterson Hamish Philpott Philip E. Putnam Joel E. Richter Rachel Rosen Melanie A. Ruffner Ekaterina Safroneeva Philipp Schreiner Alain Schoepfer Shauna Schroeder Neil Shah Rhonda F. Souza Stuart J. Spechler Jonathan M. Spergel Alex Straumann Nicholas J. Talley Nikhil Thapar Yvan Vandenplas Rajitha D. Venkatesh Mário C. Vieira Ulrike von Arnim Marjorie M. Walker Joshua B. Wechsler Barry K. Wershil Benjamin L. Wright Y. Yamada Guang‐Yu Yang Noam Zevit Marc E. Rothenberg Glenn T. Furuta Seema S. Aceves

10.1016/j.cgh.2022.02.017 article EN Clinical Gastroenterology and Hepatology 2022-02-16

Barrett's esophagus develops when refluxed gastric juice injures the esophageal squamous lining and injury heals through a metaplastic process in which intestinal-type columnar cells replace ones. The progenitor cell that gives rise to metaplasia is not known, nor it known why condition predisposed malignancy. We studied contribution of bone marrow stem development an animal model. Twenty female rats were given lethal dose irradiation followed by tail vein injection from male rats. Ten days...

10.1111/j.1442-2050.2007.00744.x article EN Diseases of the Esophagus 2007-08-02

Barrett esophagus (BE) is defined by the presence of metaplastic esophageal columnar epithelium with goblet cells within endoscopically recognizable areas esophagus. However, some carcinomas in BE, or from gastroesophageal junction region, develop mucosa devoid cells. biologic properties, pathogenesis, and risk malignancy metaplastic, nongoblet epithelium, is, essentially, unknown. In this study, 89 patients were evaluated immunohistochemically for markers intestinal differentiation, such as...

10.1097/pas.0b013e31819f57e9 article EN The American Journal of Surgical Pathology 2009-06-24
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