Evidence map›Paper›PMID 20336470›Full record

ArticleJournal of gastroenterology2010

Adiponectin receptors are downregulated in human gastric cancer.

Kensuke Otani, Joji Kitayama, Takao Kamei, Daisuke Soma, Hideyo Miyato, Toshimasa Yamauchi, Takashi Kadowaki, Hirokazu Nagawa

Abstract read
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In one paragraph

Article in Journal of gastroenterology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.5field-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

10 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. microRNA-423-3p promotes tumor progression via modulation of AdipoR2 in laryngeal carcinoma.International journal of clinical and experimental pathology · 2014
    Article
  5. Article
  6. Article
  7. Role of adiponectin and its receptors in cancer.Cancer biology & medicine · 2012
    Article
  8. Article
  9. Adiponectin receptor-1 expression is associated with good prognosis in gastric cancer.Journal of experimental & clinical cancer research : CR · 2011
    Article
  10. 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

8 authors at 1 institution in 1 country.

Kensuke OtaniDepartment of Surgical Oncology, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan. wowtani@tune.ocn.ne.jp
Joji Kitayama
Takao Kamei
Daisuke Soma
Hideyo Miyato
Toshimasa Yamauchi
Takashi Kadowaki
Hirokazu Nagawa
The University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAdiponectin has been shown to have suppressive effects on tumor development, but the expression of adiponectin receptors in tumor tissue has not been fully elucidated. The purpose of this study was to quantitatively evaluate the expression of two adiponectin receptors, AdipoR1 and AdipoR2, in gastric cancer tissue.

methodsThe mRNA levels of AdipoR1 and AdipoR2 were evaluated by quantitative reverse transcription polymerase chain reaction (RT-PCR) and immunohistochemical staining in 67 gastric cancer tissues and their normal counterparts. In addition, the effects of cytokines on AdipoR1 and AdipoR2 expression in cultured gastric cancer cells were examined.

resultsAs compared to findings in the normal counterparts, AdipoR1 mRNA expression, standardized by β-actin mRNA, tended to be lower (cancer 0.488 ± 0.039, normal 0.955 ± 0.281, p = 0.0726) and AdipoR2 expression was significantly lower (0.818 ± 0.081, 1.500 ± 0.222, p = 0.0035) in gastric cancer tissue. Immunohistochemical examination showed the same tendency for AdipoR1 and AdipoR2 expression in epithelial cells. Moreover, AdipoR2 was strongly expressed in interstitial cells. However, the expression levels of these receptors did not show a strong correlation with various pathological factors. An in vitro experiment using two gastric cancer cell lines, MKN-74 and NUGC-3, showed that the expression levels of AdipoR1 and AdipoR2 were significantly decreased by transforming growth factor (TGF)-β in a dose-dependent manner.

conclusionsTwo major adiponectin receptors were decreased in gastric cancer as compared to findings in normal gastric epithelium. TGF-β may be involved in this receptor downregulation. This downregulation may be an ideal strategy for cancer cells to escape the antiproliferative effects of adiponectin in the initial phase of tumor development.

Indexed as

Down-RegulationAdultAgedAged, 80 and overCell Line, TumorDose-Response Relationship, DrugFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedReceptors, AdiponectinReverse Transcriptase Polymerase Chain ReactionRNA, MessengerStomach NeoplasmsTransforming Growth Factor betaADIPOR1 protein, humanADIPOR2 protein, humanReceptors, AdiponectinRNA, MessengerTransforming Growth Factor beta

Identifiers

PMID20336470
OpenAlexW2051616139

What OpenQuestion holds

Textmetadata
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.