Evidence map›Paper›PMID 35377131›Full record

ArticleGenes & genomics2022

Prognostic significance of three endothelial nitric oxide synthase (eNOS) polymorphisms and metabolic syndrome (MetS) in patients with colorectal cancer.

Eun Ju Ko, Eo Jin Kim, Hye Jung Cho, Jisu Oh, Han Sung Park, Chang Soo Ryu, Jung Oh Kim, Hak Hoon Jun, So Young Chong, Jong Woo Kim and 1 more

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Article in Genes & genomics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

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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

4 citing papers in PubMed, 6 citations in OpenAlex.

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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

11 authors at 4 institutions in 1 country.

Eun Ju Ko *Department of Biomedical Science, College of Life Science, CHA University, Seongnam, South Korea.
Eo Jin Kim *Division of Hematology/Oncology, Department of Internal Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea.
Hye Jung ChoDepartment of Surgery, CHA Bundang Medical Center, CHA University, Seongnam, South Korea.
Jisu OhDepartment of Internal Medicine, CHA Bundang Medical Center, CHA University, Seongnam, South Korea.
Han Sung ParkDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam, South Korea.
Chang Soo RyuDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam, South Korea.
Jung Oh KimDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam, South Korea.
Hak Hoon JunDepartment of Surgery, CHA Bundang Medical Center, CHA University, Seongnam, South Korea.
So Young ChongDepartment of Internal Medicine, CHA Bundang Medical Center, CHA University, Seongnam, South Korea.
Jong Woo KimDepartment of Surgery, CHA Bundang Medical Center, CHA University, Seongnam, South Korea. kjw@cha.ac.kr.
Nam Keun KimDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam, South Korea. nkkim@cha.ac.kr.ORCID 0000-0003-0541-3528
CHA University Bundang Medical Center · KRCHA University · KRKangbuk Samsung Hospital · KRYonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPolymorphisms of endothelial nitric oxide synthases (eNOS) have been associated with cancer susceptibility. Also, metabolic syndrome is associated with cancer malignancy. However, the effect of eNOS polymorphisms and metabolic syndrome on colorectal cancer (CRC) prognosis remains unclear.

objectiveTo investigated whether three genetic polymorphisms (- 786 T > C rs2070744, 4a4b rs869109213, and 894G > T rs1799983) in the eNOS and metabolic syndrome (MetS) were associated with CRC patient survival.

methodsWe genotyped three polymorphisms of eNOS (- 786 T > C, 4a4b, and 894G > T) in 312 CRC cases from the Korean population by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis.

resultsAlthough the three eNOS polymorphisms were not causative of MetS, the TT genotype of the 894G > T polymorphism was associated with a worse survival rate compared with the GG genotype in the CRC group with MetS than in the CRC group without MetS (5-years survival; adjusted HR = 54.777; 95% CI 5.073-591.487 and RFS; adjusted HR = 14.909; 95% CI 1.571-141.528).

conclusionsThe eNOS polymorphisms were not associated with metabolic syndrome prevalence in CRC patients. However, our findings suggest that the eNOS 894G > T polymorphism with MetS was associated with poor clinical outcomes.

Indexed as

Colorectal NeoplasmsMetabolic SyndromeHumansNitric Oxide Synthase Type IIIPolymorphism, GeneticPrognosisNitric Oxide Synthase Type IIINOS3 protein, humanColorectal cancereNOSMetabolic syndromeNitric oxidePolymorphismSusceptibility

Identifiers

PMID35377131
OpenAlexW4225619885

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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.