Evidence map›Paper›PMID 24748501›Full record

ArticleGastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association2015

Predictive value of CHFR and MLH1 methylation in human gastric cancer.

Yazhuo Li, Yunsheng Yang, Youyong Lu, James G Herman, Malcolm V Brock, Po Zhao, Mingzhou Guo

Open access · bronzeAbstract read
In one paragraph

Article in Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 2 pooled it
3.0field-weighted citation impact, top 8% 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

50 citing papers in PubMed, 2 syntheses or guidelines pooled it, 76 citations in OpenAlex.

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  10. Gastric Cancer in the Era of Epigenetics.International journal of molecular sciences · 2024
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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

7 authors at 3 institutions in 2 countries.

Yazhuo LiDepartment of Pathology, Chinese PLA General Hospital, Haitangwan Town, Sanya, 572000, Hainan, China.
Yunsheng Yang
Youyong Lu
James G Herman
Malcolm V Brock
Po Zhao
Mingzhou Guo
Chinese PLA General Hospital · CNJohns Hopkins University · USPeking University · CN

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
MIF in progression and treatment of ALDU01AA020821 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI NAGY, LAURA E. · 2012 to 2016
$2.1M
CHFR Methylation for Predicting Taxane Sensitivity in Lung and Esophageal CancerR33CA127055 · NCI · JOHNS HOPKINS UNIVERSITY · PI HERMAN, JAMES G. · 2008 to 2011
$1.1M
Corticostriatal networks and NMDAR mediation of habitual and flexible actionK22AA020303 · NIAAA · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI BRIGMAN, JONATHAN L · 2011 to 2013
$486k
CHFR Methylation for Predicting Taxane Sensitivity in Lung and Esophageal CancerR21CA127055 · NCI · JOHNS HOPKINS UNIVERSITY · PI HERMAN, JAMES G. · 2007 to 2007
$230k
NCI NIH HHS P30 CA006973NCI NIH HHS R21 CA127055NCI NIH HHS R33 CA127055NIAAA NIH HHS K22 AA020303NIAAA NIH HHS U01 AA020821
6 · The paper itself

Abstract

backgroundGastric carcinoma (GC) has one of the highest mortality rates of cancer diseases and has a high incidence rate in China. Palliative chemotherapy is the main treatment for advanced gastric cancer. It is necessary to compare the effectiveness and toxicities of different regimens. This study explores the possibility of methylation of DNA damage repair genes serving as a prognostic and chemo-sensitive marker in human gastric cancer.

methodsThe methylation status of five DNA damage repair genes (CHFR, FANCF, MGMT, MLH1, and RASSF1A) was detected by nested methylation-specific PCR in 102 paraffin-embedded gastric cancer samples. Chi-square or Fisher's exact tests were used to evaluate the association of methylation status and clinic-pathological factors. The Kaplan-Meier method and Cox proportional hazards models were employed to analyze the association of methylation status and chemo-sensitivity.

resultsThe results indicate that CHFR, MLH1, RASSF1A, MGMT, and FANCF were methylated in 34.3% (35/102), 21.6% (22/102), 12.7% (13/102), 9.8% (10/102), and 0% (0/102) of samples, respectively. No association was found between methylation of CHFR, MLH1, RASSF1A, MGMT, or FANCF with gender, age, tumor size, tumor differentiation, lymph node metastasis, and TNM stage. In docetaxel-treated gastric cancer patients, resistance to docetaxel was found in CHFR unmethylated patients by Cox proportional hazards model (HR 0.243, 95% CI, 0.069-0.859, p = 0.028), and overall survival is longer in the CHFR methylated group compared with the CHFR unmethylated group (log-rank, p = 0.036). In oxaliplatin-treated gastric cancer patients, resistance to oxaliplatin was found in MLH1 methylated patients (HR 2.988, 95% CI, 1.064-8.394, p = 0.038), and overall survival was longer in the MLH1 unmethylated group compared with the MLH1 methylated group (log-rank, p = 0.046).

conclusionsCHFR is frequently methylated in human gastric cancer, and CHFR methylation may serve as a docetaxel-sensitive marker. MLH1 methylation was related to oxaliplatin resistance in gastric cancer patients.

Indexed as

DNA MethylationAdaptor Proteins, Signal TransducingAdultAgedAntineoplastic Combined Chemotherapy ProtocolsCell Cycle ProteinsDrug Resistance, NeoplasmFemaleFollow-Up StudiesHumansIntestinal NeoplasmsLymphatic MetastasisMaleMiddle AgedMutL Protein Homolog 1Neoplasm InvasivenessAdaptor Proteins, Signal TransducingCell Cycle ProteinsCHFR protein, humanMLH1 protein, humanMutL Protein Homolog 1Neoplasm ProteinsNuclear ProteinsPoly-ADP-Ribose Binding ProteinsUbiquitin-Protein Ligases

Identifiers

PMID24748501
PMCPMC4894312
OpenAlexW2021200936

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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.