Evidence map›Paper›PMID 34948208›Full record

ArticleInternational journal of molecular sciences2021

The Small-Molecule Wnt Inhibitor ICG-001 Efficiently Inhibits Colorectal Cancer Stemness and Metastasis by Suppressing MEIS1 Expression.

Jang-Hyun Choi, Tae-Young Jang, So-El Jeon, Jee-Heun Kim, Choong-Jae Lee, Hyeon-Ji Yun, Ji-Youn Jung, So-Yeon Park, Jeong-Seok Nam

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. 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
1.5field-weighted citation impact, top 17% 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, 30 citations in OpenAlex.

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  7. Targeting CBP and p300: Emerging Anticancer Agents.Molecules (Basel, Switzerland) · 2024
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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

9 authors at 2 institutions in 1 country.

Jang-Hyun ChoiSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 61005, Korea.
Tae-Young JangSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 61005, Korea.
So-El JeonSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 61005, Korea.
Jee-Heun KimSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 61005, Korea.
Choong-Jae LeeSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 61005, Korea.
Hyeon-Ji YunSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 61005, Korea.
Ji-Youn JungDepartment of Companion and Laboratory Animal Science, Kongju National University, Gongju 32439, Korea.ORCID 0000-0002-8153-4455
So-Yeon ParkSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 61005, Korea.ORCID 0000-0002-5749-3120
Jeong-Seok NamSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 61005, Korea.ORCID 0000-0001-9753-6095
Gwangju Institute of Science and Technology · KRKongju National University · KR

Funding

Gwangju Institute of Science and Technology "GIST Research Institute (GRI) IIBR" grantGwangju Institute of Science and Technology the GIST Research Institute GIST-CNUH Research Collaboration grantGwangju Institute of Science and Technology the GIST Young Scientist Research Project grantNational Research Foundation of Korea 2020R1A2B5B03094382National Research Foundation of Korea 2020R1C1C1010758National Research Foundation of Korea NRF-2016R1A5A1007318
6 · The paper itself

Abstract

Recurrence and metastasis remain major obstacles in colorectal cancer (CRC) treatment. Recent studies suggest that a small subpopulation of cells with a self-renewal ability, called cancer stem-like cells (CSCs), promotes recurrence and metastasis in CRC. Unfortunately, no CSC inhibitor has been demonstrated to be more effective than existing chemotherapeutic drugs, resulting in a significant unmet need for effective CRC therapies. In this study, transcriptomic profiling of metastatic tumors from CRC patients revealed significant upregulation in the Wnt pathway and stemness genes. Thus, we examined the therapeutic effect of the small-molecule Wnt inhibitor ICG-001 on cancer stemness and metastasis. The ICG-001 treatment efficiently attenuated self-renewal activity and metastatic potential. Mechanistically, myeloid ecotropic viral insertion site 1 (MEIS1) was identified as a target gene of ICG-001 that is transcriptionally regulated by Wnt signaling. A series of functional analyses revealed that MEIS1 enhanced the CSC behavior and metastatic potential of the CRC cells. Collectively, our findings suggest that ICG-001 efficiently inhibits CRC stemness and metastasis by suppressing MEIS1 expression. These results provide a basis for the further clinical investigation of ICG-001 as a targeted therapy for CSCs, opening a new avenue for the development of novel Wnt inhibitors for the treatment of CRC metastasis.

Indexed as

AnimalsBridged Bicyclo Compounds, HeterocyclicCell Line, TumorColorectal NeoplasmsGene Expression ProfilingHCT116 CellsHT29 CellsHumansMaleMiceMice, Inbred NODMyeloid Ecotropic Viral Integration Site 1 ProteinNeoplastic Stem CellsPyrimidinonesSmall Molecule LibrariesTranscription, GeneticBridged Bicyclo Compounds, HeterocyclicICG 001MEIS1 protein, humanMyeloid Ecotropic Viral Integration Site 1 ProteinPyrimidinonesSmall Molecule Librariescancer stem-like cellscolorectal cancerICG-001MEIS1metastasisWnt

Identifiers

PMID34948208
PMCPMC8704261
OpenAlexW4200281250

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.