Evidence map›Paper›PMID 31432248›Full record

ArticleMedical molecular morphology2020

Expression of fatty-acid-binding protein 5 in intrahepatic and extrahepatic cholangiocarcinoma: the possibility of different energy metabolisms in anatomical location.

Risa Nakagawa, Nguyen Canh Hiep, Hirofumi Ouchi, Yasunori Sato, Kenichi Harada

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Article in Medical molecular morphology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Risa NakagawaDepartment of Human Pathology, Kanazawa University Graduate School of Medical Science, Kanazawa, 920-8640, Japan.
Nguyen Canh HiepDepartment of Human Pathology, Kanazawa University Graduate School of Medical Science, Kanazawa, 920-8640, Japan.
Hirofumi OuchiDepartment of Human Pathology, Kanazawa University Graduate School of Medical Science, Kanazawa, 920-8640, Japan.
Yasunori SatoDepartment of Human Pathology, Kanazawa University Graduate School of Medical Science, Kanazawa, 920-8640, Japan.
Kenichi HaradaDepartment of Human Pathology, Kanazawa University Graduate School of Medical Science, Kanazawa, 920-8640, Japan. kenichih@med.kanazawa-u.ac.jp.ORCID http://orcid.org/0000-0002-6451-0638
Kanazawa University · JP

Funding

Ministry of Education, Culture, Sports, Science and Technology of Japan 17H04058
6 · The paper itself

Abstract

The biliary tract cancer (BTC) covers a range of carcinomas, including intrahepatic cholangiocarcinoma (ICC), cholangiolocellular carcinoma (CoCC), perihilar cholangiocarcinoma (perihilar CC), extrahepatic cholangiocarcinoma (ECC), and gallbladder cancer (GBC), defined according to the anatomical location. These adenocarcinomas mostly comprise biliary epithelial cell-derived malignant cells. In addition to anatomical differences, there are morphological and biological differences in BTC starting from embryonic development of the tissues extending to physiological differences. Fatty acid-binding proteins (FABPs) are closely associated with the energy metabolism. Using surgical specimens from 74 BTCs, we performed immunohistochemistry for FABP5 and its associated molecules, including peroxisome proliferator-activated receptor γ (PPARγ), PPARγ coactivator 1 (PGC-1), and estrogen-related receptor α (ERRα). We found that the expression patterns of small BTCs (ICC and CoCC) considerably differed from those of large BTCs (perihilar CC, ECC, and GBC). Expression of FABP5 and PGC-1 in large BTCs was high compared with those of small BTCs, but no difference in the expression of PPARγ and ERRα was observed. FABP5 appears to play a role in malignant progression in large BTCs. Small and large BTCs possess different energy metabolism systems owing to their different anatomical locations and course of carcinogenesis, although all BTCs originate from biliary epithelial cells.

Indexed as

Gene Expression Regulation, NeoplasticAdenocarcinomaBile Duct NeoplasmsCholangiocarcinomaEnergy MetabolismEpithelial CellsERRalpha Estrogen-Related ReceptorFatty Acid-Binding ProteinsGallbladder NeoplasmsHumansOrgan SpecificityPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPPAR gammaReceptors, EstrogenERRalpha Estrogen-Related ReceptorFABP5 protein, humanFatty Acid-Binding ProteinsPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPPAR gammaPPARGC1A protein, humanPPARG protein, humanReceptors, EstrogenBiliary tract cancerEnergy metabolismExtrahepatic cholangiocarcinomaFatty-acid-binding protein 5Intrahepatic cholangiocarcinoma

Identifiers

PMID31432248
OpenAlexW2969433154

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.