Evidence map›Paper›PMID 28640361›Full record

ArticleCancer2017

Global and targeted serum metabolic profiling of colorectal cancer progression.

Yin Long, Beatriz Sanchez-Espiridion, Moubin Lin, Lindsey White, Lopa Mishra, Gottumakkala S Raju, Scott Kopetz, Cathy Eng, Michelle A T Hildebrandt, David W Chang and 3 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 45 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 2 pooled it
2.6field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 2 syntheses or guidelines pooled it, 70 citations in OpenAlex.

  1. Colorectal neoplasia-specific amino acid profiles and their diagnostic potential: a systematic review.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Pooled it
  2. Pooled it
  3. Trial
  4. Causal relationships of inflammatory cytokines and serum metabolites with colorectal carcinoma: A Mendelian randomization study.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2026
    Article
  5. Article
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  7. Gut microbes · 2025
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  16. IncreasedExperimental and therapeutic medicine · 2023
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  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 2 countries.

Yin LongDepartment of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Beatriz Sanchez-EspiridionDepartment of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Moubin LinCenter for Translational Medicine, Yangpu Hospital, Tongji University School of Medicine, Shanghai, China.
Lindsey WhiteDepartment of Pharmaceutical Sciences, Texas Southern University, Houston, Texas.
Lopa MishraDepartment of Gastroenterology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Gottumakkala S RajuDepartment of Gastroenterology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Scott KopetzDepartment of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cathy EngDepartment of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Michelle A T HildebrandtDepartment of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
David W ChangDepartment of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Yuanqing YeDepartment of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Dong LiangDepartment of Pharmaceutical Sciences, Texas Southern University, Houston, Texas.
Xifeng WuDepartment of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID http://orcid.org/0000-0001-5174-3769
The University of Texas MD Anderson Cancer Center · USTexas Southern University · USTongji University · CN

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Targeting CDK4 in TGS-B Inactivated Gastrointestinal CancersP01CA130821 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI REDDY, E PREMKUMAR · 2008 to 2013
$6.9M
Genetic Susceptibility Modifiers in Renal Cell CarcinomaR01CA098897 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI WU, XIFENG · 2003 to 2007
$2.5M
Molecular Mechanisms and Translational studies in Colon CancerI01BX003732 · VA · U.S. DEPT/VETS AFFAIRS MEDICAL CENTER · PI MISHRA, LOPA · 2017 to 2019
–
BLRD VA I01 BX003732NCI NIH HHS P01 CA130821NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA098897
6 · The paper itself

Abstract

backgroundPatients with colorectal adenoma polyps (PLPs) are at higher risk for developing colorectal cancer (CRC). However, the development of improved and robust biomarkers to enable the screening, surveillance, and early detection of PLPs and CRC continues to be a challenge. The aim of this study was to identify biomarkers of progression to CRC through metabolomic profiling of human serum samples with a multistage approach.

methodsMetabolomic profiling was conducted with the Metabolon platform for 30 CRC patients, 30 PLP patients, and 30 control subjects, and this was followed by the targeted validation of the top metabolites in an additional set of 50 CRC patients, 50 PLP patients, and 50 controls with liquid chromatography-tandem mass spectrometry. Unconditional multivariate logistic regression models, adjusted for covariates, were used to evaluate associations with PLP and CRC risk.

resultsFor the discovery phase, 404 serum metabolites were detected, with 50 metabolites showing differential levels between CRC patients, PLP patients, and controls (P for trend < .05). After validation, the 3 top metabolites (xanthine, hypoxanthine, and d-mannose) were validated: lower levels of xanthine and hypoxanthine and higher levels of d-mannose were found in PLP and CRC cases versus controls. A further exploratory analysis of metabolic pathways revealed key roles for the urea cycle and caffeine metabolism associated with PLP and CRC risk. In addition, a joint effect of the top metabolites with smoking and a significant interaction with the body mass index were observed. An analysis of the ratio of hypoxanthine levels to xanthine levels indicated an association with CRC progression.

conclusionsThese results suggest the potential utility of circulating metabolites as novel biomarkers for the early detection of CRC. Cancer 2017;123:4066-74. © 2017 American Cancer Society.

Indexed as

AdenomaAdultAgedCaffeineCase-Control StudiesChromatography, LiquidColonic PolypsColorectal NeoplasmsDisease ProgressionFemaleHumansHypoxanthineIntestinal PolypsLogistic ModelsMaleMannoseCaffeineHypoxanthineMannoseUreaXanthineadenoma polypscolorectal cancerd-mannosemetabolomic profilingxanthine/hypoxanthine ratio

Identifiers

PMID28640361
PMCPMC5626581
OpenAlexW2666273095

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.