Evidence map›Paper›PMID 32143715›Full record

ArticleCell communication and signaling : CCS2020

Small molecule-induced simultaneous destabilization of β-catenin and RAS is an effective molecular strategy to suppress stemness of colorectal cancer cells.

Yong-Hee Cho, Eun Ji Ro, Jeong-Su Yoon, Dong-Kyu Kwak, Jaebeom Cho, Dong Woo Kang, Ho-Young Lee, Kang-Yell Choi

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Cell communication and signaling : CCS, 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
0.7field-weighted citation impact, top 29% 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, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Cardiovascular diagnosis and therapy · 2023
    Article
  4. Review
  5. Article
  6. Emerging drug targets for colon cancer: A preclinical assessment.Expert opinion on therapeutic targets · 2022
    Review
  7. The Wnt Signalling Pathway: A Tailored Target in Cancer.International journal of molecular sciences · 2020
    Review
  8. 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

8 authors at 3 institutions in 1 country.

Yong-Hee ChoTranslational Research Center for Protein Function Control, Yonsei University, Seoul, South Korea.
Eun Ji RoTranslational Research Center for Protein Function Control, Yonsei University, Seoul, South Korea.
Jeong-Su YoonTranslational Research Center for Protein Function Control, Yonsei University, Seoul, South Korea.
Dong-Kyu KwakTranslational Research Center for Protein Function Control, Yonsei University, Seoul, South Korea.
Jaebeom ChoCollege of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, South Korea.
Dong Woo KangMedpacto Inc., Borim building, 92 myeongdal Ro, Seocho-gu, Seoul, South Korea.
Ho-Young LeeCollege of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, South Korea.
Kang-Yell ChoiTranslational Research Center for Protein Function Control, Yonsei University, Seoul, South Korea. kychoi@yonsei.ac.kr.ORCID 0000-0002-0952-3276
Yonsei University · KRSeoul National University · KRBoditech Med (South Korea) · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCancer stem cells (CSCs), the major driver of tumorigenesis, is a sub-population of tumor cells responsible for poor clinical outcomes. However, molecular mechanism to identify targets for controlling CSCs is poorly understood.

methodsGene Set Enrichment Analyses (GSEA) of Wnt/β-catenin and RAS signaling pathways in stem-like subtype of colorectal cancer (CRC) patients were performed using two gene expression data set. The therapeutic effects of destabilization of β-catenin and RAS were tested by treatment of small molecule KYA1797K using CRC patient derived cells.

resultsTreatment with KYA1797K, a small molecule that destabilizes both β-catenin and RAS via Axin binding, effectively suppresses the stemness of CSCs as shown in CRC spheroids and small intestinal tumors of Apc

conclusionOur results suggest that destabilization of both β-catenin and RAS is a potential therapeutic strategy for controlling stemness of CRC cells. Video abstract.

Indexed as

Antineoplastic AgentsThiazolidinesAnimalsbeta CateninCarcinogenesisCell Line, TumorCell Transformation, NeoplasticColorectal NeoplasmsGene Expression Regulation, NeoplasticHumansMiceMice, Inbred C57BLNeoplastic Stem CellsOrganoidsPrimary Cell CultureProto-Oncogene Proteins p21(ras)Antineoplastic Agentsbeta CateninCTNNB1 protein, humanKRAS protein, humanKYA1797KProto-Oncogene Proteins p21(ras)ThiazolidinesCancer stem cellsDestabilizationKYA1797KRASβ-Catenin

Identifiers

PMID32143715
PMCPMC7060567
OpenAlexW3011112837

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.