Summary of Study ST001423
This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR000730. The data can be accessed directly via it's Project DOI: 10.21228/M89X1C This work is supported by NIH grant, U2C- DK119886.
See: https://www.metabolomicsworkbench.org/about/howtocite.php
This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.
| Study ID | ST001423 |
| Study Title | Aspirin Metabolomics in Colorectal Cancer Chemoprevention - blood (part-III) |
| Study Summary | Substantial evidence supports the effectiveness of aspirin for cancer chemoprevention in addition to its well established role in cardiovascular protection. In recent meta-analyses of randomized controlled trials in human, daily aspirin use reduced incidence, metastasis and mortality from several common types of cancer, especially colorectal cancer. The mechanism(s) by which aspirin exerts an anticancer benefit is uncertain; numerous effects have been described involving both cyclooxygenase-dependent and -independent pathways. The goal of this research is to elucidate the key metabolic changes that are responsible for the anticancer effects of aspirin in humans using untargeted metabolomics analysis. Metabolomics, or global metabolite profiling, is an emerging discipline that has the potential to transform the study of pharmaceutical agents. Our innovative approach will use high-resolution mass spectroscopy to detect thousands of metabolites in blood plasma that were collected from participants in the Aspirin/Folate Polyp Prevention Study, a randomized, double-blind, placebo-controlled trial of aspirin for the prevention of colorectal adenomas. Participants in the trial were assigned with equal probability to three aspirin treatment arms (placebo, 81mg, or 325mg daily). Over the three-year period, 81mg/day of aspirin reduced the risk of adenomas, whereas the 325 mg/day dose had less effect. The aims of the current proposal are to identify metabolomic signatures, including specific metabolites and metabolic pathways, that are associated with aspirin treatment in blood after three years of randomized aspirin treatment; and then to assess the associations of these metabolic signatures with adenoma risk and whether they mediate the reductions in risk due to 81 mg/day aspirin treatment. We will prioritize metabolites for study by evaluating metabolite levels in patients from the placebo and treatment arms while controlling the false discovery rate, use correlation analysis to enhance identification of relevant metabolic modules associated with these prioritized metabolites, and apply pathway mapping with post-hoc application of ion dissociation spectroscopy to representative metabolites to confirm pathway identification. Because aspirin is a multifunctional drug that is thought to modify numerous pathways with potential roles in carcinogenesis, a global discovery-based metabolomics approach is the best way to identify its key activities. The public health significance of this work is substantial because understanding the mechanism of aspirin's anticancer effects is key to optimizing its use and to the development of novel drugs targeting the metabolic pathways identified. |
| Institute | Emory University |
| Department | School of Medicine |
| Laboratory | Clincal Biomarkers Laboratory |
| Last Name | Uppal |
| First Name | Karan |
| Address | 615 Michael St, Suite 225 |
| kuppal2@emory.edu | |
| Phone | (404) 727 5027 |
| Submit Date | 2019-11-07 |
| Total Subjects | 446 |
| Study Comments | Aspirin Metabolomics Priority 2 |
| Raw Data Available | Yes |
| Raw Data File Type(s) | raw(Thermo) |
| Analysis Type Detail | LC-MS |
| Release Date | 2020-07-20 |
| Release Version | 1 |
Select appropriate tab below to view additional metadata details:
Factors:
Subject type: Human; Subject species: Homo sapiens (Factor headings shown in green)
| mb_sample_id | local_sample_id | Sex | Treatment |
|---|---|---|---|
| SA119238 | 400106839_1 | F | 325mg |
| SA119239 | 40006183_1 | F | 325mg |
| SA119240 | 40001563_1 | F | 325mg |
| SA119241 | 400106840_1 | F | 325mg |
| SA119242 | 40000678_1 | F | 325mg |
| SA119243 | 40005384_1 | F | 325mg |
| SA119244 | 40000679_1 | F | 325mg |
| SA119245 | 400106489_1 | F | 325mg |
| SA119246 | 400105909_1 | F | 325mg |
| SA119247 | 40006620_1 | F | 325mg |
| SA119248 | 40006598_1 | F | 325mg |
| SA119249 | 40007108_1 | F | 325mg |
| SA119250 | 40005829_1 | F | 325mg |
| SA119251 | 40005843_1 | F | 325mg |
| SA119252 | 40000757_1 | F | 325mg |
| SA119253 | 40015382_1 | F | 325mg |
| SA119254 | 40005670_1 | F | 325mg |
| SA119255 | 400106404_1 | F | 325mg |
| SA119256 | 40003327_1 | F | 325mg |
| SA119257 | 40000451_1 | F | 325mg |
| SA119258 | 40001317_1 | F | 325mg |
| SA119259 | 40002097_1 | F | 325mg |
| SA119260 | 40006745_1 | F | 325mg |
| SA119261 | 40002605_1 | F | 325mg |
| SA119262 | 40015408_1 | F | 325mg |
| SA119263 | 40002208_1 | F | 325mg |
| SA119264 | 40003744_1 | F | 325mg |
| SA119265 | 40000548_1 | F | 325mg |
| SA119266 | 40005824_1 | F | 325mg |
| SA119267 | 400106545_1 | F | 325mg |
| SA119268 | 40000549_1 | F | 325mg |
| SA119269 | 40015590_1 | F | 325mg |
| SA119270 | 40005735_1 | F | 325mg |
| SA119271 | 40003788_1 | F | 325mg |
| SA119272 | 40003519_1 | F | 325mg |
| SA119273 | 40005368_1 | F | 325mg |
| SA119274 | 40001038_1 | F | 325mg |
| SA119275 | 40015520_1 | F | 325mg |
| SA119276 | 40006953_1 | F | 325mg |
| SA119277 | 400105794_1 | F | 325mg |
| SA119278 | 400105795_1 | F | 325mg |
| SA119279 | 40000207_1 | F | 325mg |
| SA119280 | 40000208_1 | F | 325mg |
| SA119281 | 40006699_1 | F | 325mg |
| SA119282 | 40021544_1 | F | 325mg |
| SA119283 | 40022736_1 | F | 325mg |
| SA119284 | 40001342_1 | F | 81mg |
| SA119285 | 40002312_1 | F | 81mg |
| SA119286 | 40002174_1 | F | 81mg |
| SA119287 | 40006512_1 | F | 81mg |
| SA119288 | 400106676_1 | F | 81mg |
| SA119289 | 40005905_1 | F | 81mg |
| SA119290 | 40001423_1 | F | 81mg |
| SA119291 | 400106609_1 | F | 81mg |
| SA119292 | 40006377_1 | F | 81mg |
| SA119293 | 40005406_1 | F | 81mg |
| SA119294 | 40000837_1 | F | 81mg |
| SA119295 | 40002499_1 | F | 81mg |
| SA119296 | 40000265_1 | F | 81mg |
| SA119297 | 40005944_1 | F | 81mg |
| SA119298 | 40006562_1 | F | 81mg |
| SA119299 | 40006335_1 | F | 81mg |
| SA119300 | 40002098_1 | F | 81mg |
| SA119301 | 40000862_1 | F | 81mg |
| SA119302 | 40005493_1 | F | 81mg |
| SA119303 | 40022480_1 | F | 81mg |
| SA119304 | 40005537_1 | F | 81mg |
| SA119305 | 40003330_1 | F | 81mg |
| SA119306 | 40001792_1 | F | 81mg |
| SA119307 | 40003356_1 | F | 81mg |
| SA119308 | 40006974_1 | F | 81mg |
| SA119309 | 40005633_1 | F | 81mg |
| SA119310 | 40002197_1 | F | 81mg |
| SA119311 | 40006320_1 | F | 81mg |
| SA119312 | 40000718_1 | F | 81mg |
| SA119313 | 40002314_1 | F | 81mg |
| SA119314 | 400106736_1 | F | 81mg |
| SA119315 | 40005739_1 | F | 81mg |
| SA119316 | 40005521_1 | F | 81mg |
| SA119317 | 40005754_1 | F | 81mg |
| SA119318 | 40001351_1 | F | 81mg |
| SA119319 | 40001345_1 | F | 81mg |
| SA119320 | 40006035_1 | F | 81mg |
| SA119321 | 40001489_1 | F | 81mg |
| SA119322 | 40000606_1 | F | 81mg |
| SA119323 | 40002539_1 | F | 81mg |
| SA119324 | 40000447_1 | F | 81mg |
| SA119325 | 400106480_1 | F | 81mg |
| SA119326 | 40000448_1 | F | 81mg |
| SA119327 | 40001426_1 | F | 81mg |
| SA119328 | 40000721_1 | F | 81mg |
| SA119329 | 40022886_1 | F | 81mg |
| SA119330 | 40000872_1 | F | 81mg |
| SA119331 | 40003495_1 | F | 81mg |
| SA119332 | 40003440_1 | F | 81mg |
| SA119333 | 40015435_1 | F | 81mg |
| SA119334 | 40001756_1 | F | 81mg |
| SA119335 | 400105980_1 | F | 81mg |
| SA119336 | 40005557_1 | F | 81mg |
| SA119337 | 40003365_1 | F | 81mg |
