Evidence map›Paper›PMID 28584893›Full record

ArticlePathology oncology research : POR2018

Development of Novel Monoclonal Antibodies for Evaluation of Transmembrane Prostate Androgen-Induced Protein 1 (TMEPAI) Expression Patterns in Gastric Cancer.

Mikhail S Karbyshev, Evgeniya S Grigoryeva, Viktor V Volkomorov, Elisabeth Kremmer, Alexander Huber, Irina V Mitrofanova, Evgeniya V Kaigorodova, Marina V Zavyalova, Julia G Kzhyshkowska, Nadezda V Cherdyntseva and 1 more

Abstract read
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In one paragraph

Article in Pathology oncology research : POR, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. RETRACTED: Analysis ofCancers · 2019
    Article
  5. 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 5 institutions in 2 countries.

Mikhail S KarbyshevDepartment of Molecular Oncology and Immunology, Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences, Kooperativny Str. 5, Tomsk, Russian Federation, 634050.
Evgeniya S GrigoryevaDepartment of Molecular Oncology and Immunology, Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences, Kooperativny Str. 5, Tomsk, Russian Federation, 634050. grigorieva@oncology.tomsk.ru.
Viktor V VolkomorovDepartment of Molecular Oncology and Immunology, Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences, Kooperativny Str. 5, Tomsk, Russian Federation, 634050.
Elisabeth KremmerHelmholtz Zentrum München, German Research Center for Environmental Health, Institute of Molecular Immunology, Marchioninistr. 25, 81377, Munich, Germany.
Alexander HuberHelmholtz Zentrum München, German Research Center for Environmental Health, Institute of Molecular Immunology, Marchioninistr. 25, 81377, Munich, Germany.
Irina V MitrofanovaDepartment of Molecular Oncology and Immunology, Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences, Kooperativny Str. 5, Tomsk, Russian Federation, 634050.
Evgeniya V KaigorodovaDepartment of Pathological Anatomy and Cytology, Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences, Kooperativny Str. 5, Tomsk, Russian Federation, 634050.
Marina V ZavyalovaLaboratory for Translational Cellular and Molecular Biomedicine, Tomsk State University, 36 Lenin Ave, Tomsk, Russian Federation, 634050.
Julia G KzhyshkowskaLaboratory for Translational Cellular and Molecular Biomedicine, Tomsk State University, 36 Lenin Ave, Tomsk, Russian Federation, 634050.
Nadezda V CherdyntsevaDepartment of Molecular Oncology and Immunology, Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences, Kooperativny Str. 5, Tomsk, Russian Federation, 634050.
Evgeny L ChoynzonovDepartment of Molecular Oncology and Immunology, Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences, Kooperativny Str. 5, Tomsk, Russian Federation, 634050.
Tomsk National Research Medical Center · RUHelmholtz Zentrum München · DERussian Academy of Sciences · RUNational Research Tomsk State University · RUSiberian State Medical University · RU

Funding

Russian Fund for Basic Research 14-04-31500
6 · The paper itself

Abstract

Transmembrane prostate androgen-induced protein 1 (TMEPAI) is a single-span membrane protein, functionally involved in transforming growth factor beta signaling pathway. The particular protein presented in cells in three isoforms, which differs in the length of the soluble N-terminal extracellular domain, making it challenging for the immunochemical recognition. By using quantitative real-time polymerase chain reaction, we identified significant upregulation of PMEPA1 gene expression in malignant tissues of patients with gastric adenocarcinoma. The main part of commercially available anti-TMEPAI antibodies are having polyclonal nature or not suitable for immunocytochemical localization of target protein in tissue specimens. Hence, we decide to generate a set of novel rat monoclonal antibodies (mAb) directed against conservative C-terminal cytoplasmic epitope. Immunoblotting analysis showed that monoclonal antibodies, 2E1, 6C6, and 10A7 were able to recognize specifically target protein in transiently transfected HEK293T and CHO-K1 cells. Especially established mAb, named 10A7, showed the excellent binding ability to target protein in immunohistochemistry. By using developed antibodies, we observed pronounced expression of TMEPAI in normal gastric epithelial cells while tumor cells from gastric adenomas, and adenocarcinoma samples were mostly negative for target protein expression. Also, we found that gastric epithelium cells lose the TMEPAI expression concurrently with severe dysplasia progression, which probably caused by a mechanism involving specific microRNA.

Indexed as

Antibodies, MonoclonalAdenocarcinomaAdultAgedAnimalsAntibody SpecificityBiomarkers, TumorHumansMembrane ProteinsMiddle AgedRatsStomach NeoplasmsAntibodies, MonoclonalBiomarkers, TumorMembrane ProteinsPMEPA1 protein, humanBiomarkerGastric cancerImmunohistochemistryMonoclonal antibodyPMEPA1TMEPAI

Identifiers

PMID28584893
OpenAlexW2621518395

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.