Evidence map›Paper›PMID 38928347›Full record

ArticleInternational journal of molecular sciences2024

An SNP Marker Predicts Colorectal Cancer Outcomes with 5-Fluorouracil-Based Adjuvant Chemotherapy Post-Resection.

Hao Chien, Yu-De Chu, Yi-Ping Hsu, Chau-Ting Yeh, Ming-Wei Lai, Ming-Ling Chang, Siew-Na Lim, Chun-Wei Chen, Wey-Ran Lin

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Hao ChienDepartment of Hepatology and Gastroenterology, Linkou Chang Gung Memorial Hospital, Taoyuan 333423, Taiwan.ORCID 0009-0000-3477-8409
Yu-De ChuLiver Research Center, Linkou Chang Gung Memorial Hospital, Taoyuan 333423, Taiwan.
Yi-Ping HsuLiver Research Center, Linkou Chang Gung Memorial Hospital, Taoyuan 333423, Taiwan.
Chau-Ting YehDepartment of Hepatology and Gastroenterology, Linkou Chang Gung Memorial Hospital, Taoyuan 333423, Taiwan.
Ming-Wei LaiLiver Research Center, Linkou Chang Gung Memorial Hospital, Taoyuan 333423, Taiwan.
Ming-Ling ChangDepartment of Hepatology and Gastroenterology, Linkou Chang Gung Memorial Hospital, Taoyuan 333423, Taiwan.ORCID 0000-0003-4902-4401
Siew-Na LimDepartment of Neurology, Linkou Chang Gung Memorial Hospital, Taoyuan 333423, Taiwan.ORCID 0000-0001-6867-8449
Chun-Wei ChenDepartment of Hepatology and Gastroenterology, Linkou Chang Gung Memorial Hospital, Taoyuan 333423, Taiwan.ORCID 0000-0001-9438-0398
Wey-Ran LinDepartment of Hepatology and Gastroenterology, Linkou Chang Gung Memorial Hospital, Taoyuan 333423, Taiwan.ORCID 0000-0001-6078-1396

Funding

Chang Gung Memorial Hospital CMRPG3M2122 and CMRPG3N1461Ministry of Science and Technology, Taiwan 110-2314-B-182A-095 and 111-2314-B-182A-126
6 · The paper itself

Abstract

Colorectal cancer (CRC) is a global health concern, necessitating adjuvant chemotherapy post-curative surgery to mitigate recurrence and enhance survival, particularly in intermediate-stage patients. However, existing therapeutic disparities highlight the need for biomarker-guided adjuvant chemotherapy to achieve better CRC inhibition. This study explores the molecular mechanisms underlying the inhibition of CRC through a genome-wide association study (GWAS) focused on 5-fluorouracil (5-FU)-based adjuvant therapy in intermediate-stage CRC patients, a domain previously unexplored. We retrospectively included 226 intermediate-stage CRC patients undergoing surgical resection followed by 5-FU-based adjuvant chemotherapy. The exploration cohort comprised 31 patients, and the validation cohort included 195 individuals. Genotyping was carried out using either Axiom Genome-Wide TWB 2.0 Array Plate-based or polymerase chain reaction-based methods on genomic DNA derived from collected tissue samples. Statistical analyses involved descriptive statistics, Kaplan-Meier analyses, and Cox proportional hazard analyses. From the GWAS, potential genetic predictors,

Indexed as

Colorectal NeoplasmsFluorouracilGenome-Wide Association StudyPolymorphism, Single NucleotideAdultAgedBiomarkers, TumorChemotherapy, AdjuvantFemaleGenotypeHumansMaleMiddle AgedN-AcetylgalactosaminyltransferasesPrognosisRetrospective StudiesBiomarkers, TumorFluorouracilN-Acetylgalactosaminyltransferases5-fluorouraciladjuvant chemotherapycolorectal cancergenome-wide association studytherapeutic predictor

Identifiers

PMID38928347
PMCPMC11203489

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Registered trials

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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.