Evidence map›Paper›PMID 30343282›Full record

ArticleCancer genomics & proteomics

NOTUM Is Involved in the Progression of Colorectal Cancer.

Jong Hyuk Yoon, Dayea Kim, Jaeyoon Kim, Hyeongjoo Lee, Jaewang Ghim, Byung Jun Kang, Parkyong Song, Pann-Ghill Suh, Sung Ho Ryu, Taehoon G Lee

Open access · diamondAbstract read
In one paragraph

Article in Cancer genomics & proteomics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

16 citing papers in PubMed, 28 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

10 authors at 5 institutions in 1 country.

Jong Hyuk YoonDepartment of Neural Development and Disease, Korea Brain Research Institute, Daegu, Republic of Korea taehoon@novacelltech.com jhyoon@kbri.re.kr.
Dayea KimNew Drug Development Center, Daegu-Gyeongbuk Medical Innovation Foundation, Daegu, Republic of Korea.
Jaeyoon KimSchool of Interdisciplinary Bioscience and Bioengineering, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea.
Hyeongjoo LeeNovaCell Technology, Inc., Pohang, Republic of Korea.
Jaewang GhimNovaCell Technology, Inc., Pohang, Republic of Korea.
Byung Jun KangDepartment of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea.
Parkyong SongDepartment of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea.
Pann-Ghill SuhSchool of Life Sciences, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea.
Sung Ho RyuDepartment of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea.
Taehoon G LeeNovaCell Technology, Inc., Pohang, Republic of Korea taehoon@novacelltech.com jhyoon@kbri.re.kr.
NovaCell Technology (South Korea) · KRPohang University of Science and Technology · KRDaegu-Gyeongbuk Medical Innovation Foundation · KRKorea Brain Research Institute · KRUlsan National Institute of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere are limitations to current colorectal cancer (CRC)-specific diagnostic methods and therapies. Tumorigenesis proceeds because of interaction between cancer cells and various surrounding cells; discovering new molecular mediators through studies of the CRC secretome is a promising approach for the development of CRC diagnostics and therapies. MATERIALS AND

methodsA comparative secretomic analysis was performed using primary and metastatic human isogenic CRC cells. Proliferation was determined by MTT and thymidine incorporation assay, migration was determined by wound-healing assay (ELISA). The level of palmitoleoyl-protein carboxylesterase (NOTUM) in plasma from patients with CRC was determined by enzyme-linked immunosorbent assay.

resultsNOTUM expression was increased in metastatic cells. Proliferation was suppressed by inhibiting expression of NOTUM. Knockdown of NOTUM genes inhibited proliferation as well as migration, with possible involvement of p38 and c-JUN N-terminal kinase in this process. The result was verified in patients with CRC.

conclusionNOTUM may be a new candidate for diagnostics and therapy of CRC.

Indexed as

Cell ProliferationGene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticCell Line, TumorColorectal NeoplasmsEsterasesGene Knockdown TechniquesHumansNeoplasm MetastasisNeoplasm ProteinsEsterasesNeoplasm ProteinsNotum protein, humancolorectal cancerdiagnosismigrationNOTUMsecretomics

Identifiers

PMID30343282
PMCPMC6299789
OpenAlexW2896235972

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.