Regulation of DNA damage response in esophageal cells exposed to reflux

反流食管细胞 DNA 损伤反应的调节

• 批准号: 10293543
• 负责人: ALEXANDER I. ZAIKA
• 金额: --
• 依托单位: MIAMI VA HEALTH CARE SYSTEM
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-07-01 至 2024-09-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10293543
• 关键词: Affect; Animal Model; Animal Testing; Animals; Apoptosis; Bile fluid; Biological Process; Cell Cycle Arrest; Cell Proliferation; Cells; Chemicals; Chemopreventive Agent; Chronic; Clinical; DNA; DNA Damage; DNA Repair; DNA Sequence Alteration; Data; Development; Duct (organ) structure; Duodenum; Epithelial; Esophageal Adenocarcinoma; Esophageal Intraepithelial Neoplasia; Esophageal Tissue; Esophageal mucous membrane; Esophagus; Exposure to; Frequencies; Gastroesophageal reflux disease; Genomic Instability; Health; High Prevalence; Histologic; Human; Incidence; Individual; Inflammatory; Injury; Innate Immune Response; Laboratories; Lead; Lesion; Malignant - descriptor; Malignant Neoplasms; Malignant neoplasm of esophagus; Mediating; Metaplasia; Molecular; Mutation; Neoplasms; Neoplastic Cell Transformation; PTGS2 gene; Pathway interactions; Patients; Play; Population; Prevention; Protein Family; Proteins; Reflux; Regulation; Reporting; Research; Risk; Risk Factors; Role; Specimen; Stomach Content; Survival Rate; TP53 gene; Testing; Tissues; Tumor Suppression; Tumor Suppressor Proteins; Veterans; adduct; base; chemotherapeutic agent; drug testing; free radical oxygen; genome integrity; in vivo; innovation; insight; interest; member; mouse model; novel; novel therapeutic intervention; premalignant; prevent; response; screening; tissue injury; tumor; tumorigenesis; tumorigenic

Esophageal adenocarcinoma (EAC) poses a serious clinical problem due to the increasing incidence and limited treatment options. One of the strongest known risk factors for EAC is gastroesophageal reflux disease (GERD), a chronic digestive condition in which acidic contents from the stomach, frequently mixed with duode- nal bile, enter the esophagus resulting in esophageal tissue injury. At the cellular level, gastroesophageal re- flux is characterized by continuous damage to esophageal cell DNA that increases the mutation rate and pro- motes genomic instability. GERD is common among veterans. However, only a percentage of affected individ- uals develop neoplasia, underscoring the importance of defining mechanisms that regulate tumorigenic interac- tions. We have developed an innovative hypothesis to explain how continued reflux induces tumorigenic altera- tions in the esophagus through inhibition of the DNA Damage Response (DDR), a critical tumor suppressor mechanism that is responsible for maintaining the integrity of the genome. This hypothesis is supported by strong preliminary data generated by animal and human studies. We will expand on these novel findings by detailing the impact of GERD on the DDR. In aim 1, we will define previously unknown molecular mechanisms through which reflux inhibits the DDR. In aim 2, we will investigate the DDR regulation in the esophageal niche using animal models of esophageal reflux injury. We will also ana- lyze human clinical specimens. In aim 3, we will test various options to avert inhibition of the DDR induced by GERD in vivo. Combined, our studies will further elucidate the potential risk factors for tumorigenic alterations in the esophagus and lay the groundwork for novel therapeutic approaches that halt the development of malignant esophageal lesions.

食管腺癌（EAC）由于其发病率和预后的增加而成为一个严重的临床问题