Evidence map›Paper›PMID 31817577›Full record

ArticleNutrients2019

Bioactivity Evaluation of a Novel Formulated Curcumin.

Se-Chun Liao, Wei-Hsiang Hsu, Zi-Yi Huang, Kun-Lin Chuang, Kuan-Ting Lin, Chia-Ling Tseng, Tung-Hu Tsai, Anh-Hoang Dao, Chun-Li Su, Chi-Ying F Huang

Abstract read
In one paragraph

Article in Nutrients, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

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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

10 authors.

Se-Chun LiaoInstitute of Clinical Medicine, National Yang-Ming University, Taipei 112, Taiwan.
Wei-Hsiang HsuInstitute of Biopharmaceutical Sciences, National Yang-Ming University, Taipei 112, Taiwan.ORCID 0000-0001-5468-5859
Zi-Yi HuangInstitute of Biopharmaceutical Sciences, National Yang-Ming University, Taipei 112, Taiwan.
Kun-Lin ChuangInstitute of Biopharmaceutical Sciences, National Yang-Ming University, Taipei 112, Taiwan.
Kuan-Ting LinCold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.
Chia-Ling TsengDepartment of Human Development and Family Studies, National Taiwan Normal University, Taipei 106, Taiwan.
Tung-Hu TsaiInstitute of Traditional Medicine, School of Medicine, National Yang-Ming University, Taipei 112, Taiwan.ORCID 0000-0002-9007-2547
Anh-Hoang DaoDepartment of Formulation and Processing, National Institute of Medicinal Materials, Hanoi 100000, Vietnam.
Chun-Li SuDepartment of Human Development and Family Studies, National Taiwan Normal University, Taipei 106, Taiwan.ORCID 0000-0001-7617-2077
Chi-Ying F HuangInstitute of Clinical Medicine, National Yang-Ming University, Taipei 112, Taiwan.ORCID 0000-0003-4898-4937

Funding

Ministry of Science and Technology, Taiwan MOST 106-2320-B-003-006-MY3Ministry of Science and Technology, Taiwan MOST 107-2320-B-003-002-MY2Ministry of Science and Technology, Taiwan MOST 107-2320-B-010-040-MY3National Science Council NSC 101-2313-B-003-002-MY3Yang-Ming University YM106C024
6 · The paper itself

Abstract

Curcumin has been used as a traditional medicine and/or functional food in several cultures because of its health benefits including anticancer properties. However, poor oral bioavailability of curcumin has limited its oral usage as a food supplement and medical food. Here we formulated curcumin pellets using a solid dispersion technique. The pellets had the advantages of reduced particle size, improved water solubility, and particle porosity. This pellet form led to an improvement in curcumin's oral bioavailability. Additionally, we used the C-Map and Library of Integrated Network-Based Cellular Signatures (LINCS) Unified Environment (CLUE) gene expression database to determine the potential biological functions of formulated curcumin. The results indicated that, similar to conventional curcumin, the formulated curcumin acted as an NF-κB pathway inhibitor. Moreover, ConsensusPathDB database analysis was used to predict possible targets and it revealed that both forms of curcumin exhibit similar biological functions, including apoptosis. Biochemical characterization revealed that both the forms indeed induced apoptosis of hepatocellular carcinoma (HCC) cell lines. We concluded that the formulated curcumin increases the oral bioavailability in animals, and, as expected, retains characteristics similar to conventional curcumin at the cellular level. Our screening platform using big data not only confirms that both the forms of curcumin have similar mechanisms but also predicts the novel mechanism of the formulated curcumin.

Indexed as

Administration, OralAnimalsAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsApoptosisAurora Kinase ABiological AvailabilityCarcinoma, HepatocellularCell Line, TumorCell ProliferationCurcuminDrug Delivery SystemsHumansLiver NeoplasmsMaleRatsAntineoplastic AgentsAurora Kinase ACurcuminSorafenibaurora kinase Acurcuminformulated curcuminhepatocellular carcinomapharmacokinetics

Identifiers

PMID31817577
PMCPMC6950821

What OpenQuestion holds

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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.