The Effect of Plant Phenolic Compounds on Human Colon Epithelial Cells
curcumin
+ rutin
+ quercetin
Colonic Diseases+9
+ Digestive System Diseases
+ Digestive System Neoplasms
Prevention Study
Summary
Study start date: August 1, 1996
Actual date on which the first participant was enrolled.OBJECTIVES: Determine the response of the colonic epithelium in normal volunteers at average or above average risk of colon cancer, when given short term treatment with plant phenolics such as curcumin, rutin, and quercetin. Compare the colonic mucosal response to the plant phenolics with their response to sulindac in order to evaluate whether they share common mechanisms for colon cancer chemoprevention. Determine the lowest optimal dose for each of the three plant phenolics that is effective in modulating biomarkers of colon epithelial cell turnover and, therefore, potentially inhibiting colon cancer development. Assess the response of the colonic epithelium to curcumin in volunteers at average risk of colon cancer development. OUTLINE: This is a randomized, controlled, two part, single institution study. Patients in Part B are randomized by gender. All patients undergo flexible sigmoidoscopic exam. Part A: Patients, in cohorts of 5-10, receive one of the following five treatments in addition to the control diet: nothing (arm I), oral sulindac twice a day (arm II), oral rutin at 1 of 3 doses twice a day (arms III, IV, and V), oral quercetin at 1 of 3 doses twice a day (arms V, VI, and VII), or at 1 of 3 doses oral curcumin twice a day (arms VIII, IX, and X). Patients are first randomized to the highest doses of rutin, quercetin, and curcumin and then lower doses may be given in order to determine the minimally effective dose. Treatment is continued for 6-10 weeks. Part B: Patients are randomized to receive the control diet only (arm I) or the control diet plus oral curcumin twice a day (arm II) for 6-10 weeks. Patients are followed every 2 weeks. PROJECTED ACCRUAL: There will be 130 patients (110 in Part A and 20 in Part B) accrued into this study.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Prevention Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
DISEASE CHARACTERISTICS: Individuals at average risk (Parts A and B) or above average risk (Part A only) for development of colon cancer Average risk individuals defined as: No history of colon adenomas No strong family history of colon polyps or cancer Above average risk individuals defined as: History of one or more sporadic adenomatous polyps at least 0.5 cm in size (either tubular, tubulovillous, or villous adenomas) Have had polypectomy or refused this procedure No significant family history of adenomatous polyps, colon cancer, or hereditary nonpolyposis colorectal cancer or other hereditary colon cancer syndrome Polyps should not have had a focus of adenocarcinoma within them No history of gastrointestinal cancer outside of the large bowel No other gastrointestinal mucosal epithelial disease (e.g., Barrett's esophagus, chronic or recurrent peptic ulcer disease, celiac sprue, or other disorders of nutrient absorption) No significant asymptomatic lesions on flexible sigmoidoscopy, such as inflammation, premalignancy or malignancy PATIENT CHARACTERISTICS: Age: 18 and over Performance status: Not specified Life expectancy: Not specified Hematopoietic: No platelet or coagulation abnormalities No personal or family history of a bleeding disorder Hematopoietic concentration must not be due to significant acute or chronic disorder Hepatic: No liver disease Renal: No renal insufficiency Cardiovascular: No uncontrolled hypertension No chronic congestive heart failure No history of endocarditis No history of rheumatic fever No cardiac valve prostheses No mitral valve prolapse that requires antibiotic prophylaxis Other: HIV negative No gout No pancreatitis No other chronic viral infection No significant acute or uncontrolled chronic medical illness Generally non-smoking (no more than 4 cigarettes per week, i.e., not daily smokers) Must abstain from smoking for at least 1 month prior to enrolling in the study No alcohol consumption of greater than 2 glasses of wine or beer per day Normal weight (90-120% of optimum body weight) and body habitus No change in weight within 5-10% of body weight within the past year No history of inflammatory bowel disease (either ulcerative colitis or Crohn's disease ) No hearing or equilibrium disorders No other prior malignancy except resected carcinoma in situ of the cervix or nonmelanoma skin cancer No allergies to sulindac or tartrazine dyes or prior severe adverse reactions to nonsteroidal antiinflammatory drugs (asthma, gastrointestinal bleeding, or renal insufficiency) No potential allergy to curcumin, quercetin, or rutin No gastrointestinal bleeding Not institutionalized, mentally disabled, or incarcerated No unusually high intake of stored micronutrients or high doses of supplemental calcium or folate Not pregnant or nursing PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: Not specified Endocrine therapy: Not specified Radiotherapy: Not specified Surgery: Not specified Other: No concurrent coumadin No chronic use of nonsteroidal antiinflammatory drugs (unless they can be stopped for 3 months) No other putative colon cancer chemoprevention agents (unless they can be stopped for 3 months)
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Rockefeller University Hospital
New York, United StatesOpen Rockefeller University Hospital in Google Maps