Evidence map›Paper›PMID 27144430›Full record

ArticleOncotarget2016

Relationship between insulin-like growth factor axis gene polymorphisms and clinical outcome in advanced gastric cancer patients treated with FOLFOX.

Sung Yong Oh, Aesun Shin, Seong-Geun Kim, Jung-Ah Hwang, Seung Hyun Hong, Yeon-Su Lee, Hyuk-Chan Kwon

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 17% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Associations between IGFBP1 gene polymorphisms and the risk of preeclampsia and fetal growth restriction.Hypertension research : official journal of the Japanese Society of Hypertension · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Bioinformatic Analysis of GLI1 and Related Signaling Pathways in Chemosensitivity of Gastric Cancer.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  9. Review
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

7 authors at 5 institutions in 1 country.

Sung Yong OhDepartment of Internal Medicine, Dong-A University College of Medicine, Busan, Korea.
Aesun ShinDepartment of Preventive Medicine, Seoul National University, Korea.
Seong-Geun KimDepartment of Internal Medicine, Pusan National University Yangsan Hospital, Yangsan, Korea.
Jung-Ah HwangCancer Genomics Branch, Research Institute, National Cancer Center, Goyang, Gyeonggi-do, Korea.
Seung Hyun HongCancer Genomics Branch, Research Institute, National Cancer Center, Goyang, Gyeonggi-do, Korea.
Yeon-Su LeeCancer Genomics Branch, Research Institute, National Cancer Center, Goyang, Gyeonggi-do, Korea.
Hyuk-Chan KwonSillajen Inc., Busan, Korea.
National Cancer Center · KRDong-A University · KRPusan National University Yangsan Hospital · KRSeoul National University · KRSillaJen (South Korea) · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The insulin-like growth factor (IGF) axis plays a crucial role in proliferation, differentiation, migration, angiogenesis, and apoptosis. The present study evaluated the associations between IGF axis single-nucleotide polymorphisms (SNPs) and clinical outcomes in advanced gastric cancer (AGC) patients treated with oxaliplatin, 5-fluorouracil, and leucovorin (FOLFOX). A total of 190 patients undergoing FOLFOX chemotherapy for AGC were considered eligible for this study. Forty-four SNPs of 10 IGF axis genes were genotyped. Levels of serum IGF1 were measured using enzyme-linked immunoassays. SNPs of the IGF1R (rs12423791), and IGF1 (rs2162679, rs5742612, rs35767) genes were significantly associated with tumor response to FOLFOX. SNPs of rs4619 and rs17847203 were significantly associated with PFS (hazard ratio [HR] 0.575, 95% CI 0.385-0.858, P = 0.007; and HR 2.530, 95% CI 1.289-4.966, P = 0.007; respectively). SNPs of rs2872060 were significantly associated with OS-OS was shorter in patients carrying the TT variant than in those with the GG/GT genotypes (HR, 1.708, 95% CI 1.024-2.850, P = 0.040). The GT genotype of rs12847203 was also identified as an independent prognostic factor (HR 2.087, 95% CI 1.070-4.069, P = 0.031). These results suggest that IGF axis-pathway SNPs could be used as prognostic biomarkers of the outcome of FOLFOX chemotherapy in AGC patients. This information may facilitate identification of population subgroups that could benefit from IGF1R-targeted agents.

Indexed as

Polymorphism, Single NucleotideAdultAgedAntineoplastic Combined Chemotherapy ProtocolsFemaleFluorouracilGene FrequencyGenetic Predisposition to DiseaseGenotypeHumansInsulin-Like Growth Factor IKaplan-Meier EstimateLeucovorinMaleMiddle AgedMultivariate AnalysisFluorouracilIGF1R protein, humanInsulin-Like Growth Factor ILeucovorinOrganoplatinum CompoundsOxaliplatinReceptor, IGF Type 1Receptors, Somatomedingastric cancerinsulin-like growth factorpolymorphism

Identifiers

PMID27144430
PMCPMC5058750
OpenAlexW2344316789

What OpenQuestion holds

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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.