Evidence map›Paper›PMID 20642860›Full record

ArticleBMC cancer2010

Tumor suppressor genes are frequently methylated in lymph node metastases of breast cancers.

Weiwei Feng, Rosaria Orlandi, Naiqing Zhao, Maria Luisa Carcangiu, Elda Tagliabue, Jia Xu, Robert C Bast, Yinhua Yu

Open access · goldAbstract readComparative Study
In one paragraph

Article in BMC cancer, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 3 pooled it
2.8field-weighted citation impact, top 9% 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

32 citing papers in PubMed, 3 syntheses or guidelines pooled it, 68 citations in OpenAlex.

  1. Pooled it
  2. Aberrant promoter methylation of HIN-1 gene may contribute to the pathogenesis of breast cancer: a meta-analysis.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
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  17. Genetic variation inOncotarget · 2018
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  19. Impact ofOncology letters · 2017
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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

8 authors at 4 institutions in 3 countries.

Weiwei FengObstetrics and Gynecology Hospital of Fudan University, Shanghai, China.
Rosaria Orlandi
Naiqing Zhao
Maria Luisa Carcangiu
Elda Tagliabue
Jia Xu
Robert C Bast
Yinhua Yu
Fondazione IRCCS Istituto Nazionale dei Tumori · ITObstetrics and Gynecology Hospital of Fudan University · CNThe University of Texas MD Anderson Cancer Center · USShanghai Medical College of Fudan University · CN

Funding

NCI NIH HHS CA 80957
6 · The paper itself

Abstract

introductionMetastasis represents a major adverse step in the progression of breast carcinoma. Lymph node invasion is the most relevant prognostic factor; however little is known on the molecular events associated with lymph node metastasis process. This study is to investigate the status and role of methylation in lymph node metastatic tumors. MATERIALS AND

methodsBisulfite pyrosequencing is used to screen 6 putative tumor suppressor genes (HIN-1, RASSF1A, RIL, CDH13, RARbeta2 and E-cadherin) in 38 pairs of primary breast tumors and lymph node metastases.

resultsWe found that HIN-1, CDH13, RIL, RASSF1A and RARbeta2 were frequently methylated both in primary and metastatic tissues (range: 55.3% approximately 89.5%). E-cadherin was not frequently methylated in either setting (range: 18.4% approximately 23.7%). The methylation status of HIN-1, CDH13, RIL, and RARbeta2 in lymph nodes metastasis were correlated with that in primary tumors. The Pearson correlation values ranged from 0.624 to 0.472 (p values < 0.01 to 0.001). Interestingly, we observed an association between HIN-1 methylation and hormone status in metastatic lymph nodes. Hypermethylation of HIN-1 in metastasis lymph nodes was significantly associated with expression of ER (odds ratio, 1.070; P = 0.024) and with PR (odds ratio, 1.046; P = 0.026).

conclusionsThis study suggests that hypermethylation of tumor suppressor genes is extended from primary to metastatic tumors during tumor progression.

Indexed as

DNA MethylationGenes, Tumor SuppressorAdultAgedBreastBreast NeoplasmsCadherinsCarcinoma, Ductal, BreastCarcinoma, LobularCase-Control StudiesCytokinesDNA-Binding ProteinsFemaleHumansImmunoenzyme TechniquesLIM Domain ProteinsCadherinsCytokinesDNA-Binding ProteinsH-cadherinLIM Domain ProteinsPDLIM4 protein, humanRARB2 protein, humanRASSF1 protein, humanReceptors, EstrogenReceptors, Retinoic AcidSCGB3A1 protein, humanTumor Suppressor Proteins

Identifiers

PMID20642860
PMCPMC2914707
OpenAlexW2090011230

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.