Evidence map›Paper›PMID 24817951›Full record

ArticleInternational journal of clinical and experimental pathology2014

Enhanced serum methylated p16 DNAs is associated with the progression of gastric cancer.

Yi-Chen Wu, Ping Lv, Jing Han, Jiang-Liu Yu, Xin Zhu, Lian-Lian Hong, Wang-Yu Zhu, Qi-Ming Yu, Xin-Bao Wang, Pei Li and 1 more

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 3 pooled it
2.6field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 3 syntheses or guidelines pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  10. Direct targeting of HGF by miR-16 regulates proliferation and migration in gastric cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  11. Article
  12. Challenges of deciphering gastric cancer heterogeneity.World journal of gastroenterology · 2015
    Review
  13. Review
  14. Methylation Analysis ofAvicenna journal of medical biotechnology
    Article
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 2 institutions in 1 country.

Yi-Chen WuZhejiang Cancer Research Institute, Zhejiang Province Cancer Hospital, Zhejiang Cancer Center No. 38 Guangji Rd., Banshanqiao District, Hangzhou 310022, P. R. China.
Ping LvZhejiang Cancer Research Institute, Zhejiang Province Cancer Hospital, Zhejiang Cancer Center No. 38 Guangji Rd., Banshanqiao District, Hangzhou 310022, P. R. China.
Jing HanZhejiang Cancer Research Institute, Zhejiang Province Cancer Hospital, Zhejiang Cancer Center No. 38 Guangji Rd., Banshanqiao District, Hangzhou 310022, P. R. China.
Jiang-Liu YuZhejiang Cancer Research Institute, Zhejiang Province Cancer Hospital, Zhejiang Cancer Center No. 38 Guangji Rd., Banshanqiao District, Hangzhou 310022, P. R. China.
Xin ZhuZhejiang Cancer Research Institute, Zhejiang Province Cancer Hospital, Zhejiang Cancer Center No. 38 Guangji Rd., Banshanqiao District, Hangzhou 310022, P. R. China.
Lian-Lian HongZhejiang Cancer Research Institute, Zhejiang Province Cancer Hospital, Zhejiang Cancer Center No. 38 Guangji Rd., Banshanqiao District, Hangzhou 310022, P. R. China.
Wang-Yu ZhuZhejiang Cancer Research Institute, Zhejiang Province Cancer Hospital, Zhejiang Cancer Center No. 38 Guangji Rd., Banshanqiao District, Hangzhou 310022, P. R. China ; The Central Laboratory, Zhoushan Hospital Zhoushan 316000, P. R. China.
Qi-Ming YuDepartment of Surgical Oncology, Zhejiang Province Cancer Hospital, Zhejiang Cancer Center No. 38 Guangji Rd., Banshanqiao District, Hangzhou 310022, P. R. China.
Xin-Bao WangDepartment of Surgical Oncology, Zhejiang Province Cancer Hospital, Zhejiang Cancer Center No. 38 Guangji Rd., Banshanqiao District, Hangzhou 310022, P. R. China.
Pei LiDepartment of Pathophysiology, School of Basic Medical Sciences, Zhengzhou University Zhengzhou 450052, China.
Zhi-Qiang LingZhejiang Cancer Research Institute, Zhejiang Province Cancer Hospital, Zhejiang Cancer Center No. 38 Guangji Rd., Banshanqiao District, Hangzhou 310022, P. R. China.
Zhejiang Cancer Hospital · CNZhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe present study is to evaluate the effect of methylated p16 on the progression in patients with gastric cancer (GC), and develop a useful biomarker for predicting patient's prognosis. DESIGN AND

methodsMethylation status of p16 in GC, their corresponding para-cancerous histological normal tissues (PCHNTs), preoperative peritoneal washes (PPWs) and serum were assessed using real-time methylation specific-PCR (MSP).

resultsThe frequency of p16 methylation was significantly higher in GC tissues (85.9%; 79/92) than that in paired PCHNTs (12.0%; 11/92) (P<0.0001). p16 methylation correlated closely with lymph node metastasis, peritoneal metastasis, TNM stage, et al (all P<0.05). Both frequency of p16 methylation in PPWs and serum were 79.7% (63/92). The Aζ value of the receiver-operator characteristic curve for methylated p16 was 0.899 for serum and PPWs, compared to that in GC tissues. The patients with elevated methylated p16 levels in tumor tissues had poorer disease-free survival (DFS) rates than those without (P=0.042). There is a narrow significant difference in median survival time of more than 30 months between patients with and without preoperatively detectable methylated p16 in serum (P=0.057). Methylated p16 in PPWs revealed no significant association with survival (P=0.129). Cox regression analysis showed that serum methylated p16 DNAs was an independent risk factor for GC patients, with a remarkable decrease in DFS 30 months after surgical resection of the gastric tumor.

conclusionsSerum methylated p16 DNAs might serve as a potential biomarker for the progression and a prognostic factor in gastric cancer patients.

Indexed as

Disease ProgressionDNA MethylationAdenocarcinomaAdultAgedBiomarkers, TumorCyclin-Dependent Kinase Inhibitor p16DNAFemaleHumansLymphatic MetastasisMaleMiddle AgedNeoplasm ProteinsPeritoneal NeoplasmsPrognosisBiomarkers, TumorCDKN2A protein, humanCyclin-Dependent Kinase Inhibitor p16DNANeoplasm ProteinsGastric carcinomamethylationp16 geneperitoneal micrometastasisprognosis

Identifiers

PMID24817951
PMCPMC4014235
OpenAlexW1466548248

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.