Evidence map›Paper›PMID 33720534›Full record

ArticleFEBS open bio2021

CD133 prevents colon cancer cell death induced by serum deprivation through activation of Akt-mediated protein synthesis and inhibition of apoptosis.

Yusuke Mori, Ayaka Takeuchi, Kengo Miyagawa, Hiroyuki Yoda, Hiroaki Soda, Yoshihiro Nabeya, Naoko Watanabe, Toshinori Ozaki, Osamu Shimozato

Open access · goldAbstract read
In one paragraph

Article in FEBS open bio, 2021. 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
0.5field-weighted citation impact, top 32% 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, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Can CD133 Be Regarded as a Prognostic Biomarker in Oncology: Pros and Cons.International journal of molecular sciences · 2023
    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

9 authors at 2 institutions in 1 country.

Yusuke MoriLaboratory of Oncogenomics, Chiba Cancer Center Research Institute, Japan.
Ayaka TakeuchiLaboratory of Oncogenomics, Chiba Cancer Center Research Institute, Japan.
Kengo MiyagawaLaboratory of Oncogenomics, Chiba Cancer Center Research Institute, Japan.
Hiroyuki YodaLaboratory of Innovative Cancer Therapeutics, Chiba Cancer Center Research Institute, Japan.ORCID 0000-0002-5528-8940
Hiroaki SodaDepartment of Esophago-Gastrointestinal Surgery, Chiba Cancer Center Hospital, Japan.
Yoshihiro NabeyaDepartment of Esophago-Gastrointestinal Surgery, Chiba Cancer Center Hospital, Japan.
Naoko WatanabeDepartment of Biomolecular Science, Faculty of Science, Toho University, Funabashi, Japan.
Toshinori OzakiLaboratory of Oncogenomics, Chiba Cancer Center Research Institute, Japan.
Osamu ShimozatoLaboratory of Oncogenomics, Chiba Cancer Center Research Institute, Japan.ORCID 0000-0002-7508-5809
Chiba Cancer Center · JPToho University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the early phase of tumorigenesis, primary malignant cells survive within a low nutrition environment caused by a poorly organized vascular system. Here, we sought to determine the functional significance of CD133 in the survival of cancer cells under nutrient-poor conditions. Knockdown and overexpression experiments demonstrated that CD133 suppresses colon cancer cell death induced by serum deprivation through activation of Akt-mediated anti-apoptosis and protein synthesis pathways. Furthermore, serum deprivation increased the amount of endogenous CD133 protein, which was regulated at least in part by phosphoinositide 3-kinase. Thus, it is highly likely that CD133 contributes to the acquisition/maintenance of the resistance to stress arising from nutrient deficiency in early avascular tumor tissues.

Indexed as

AC133 AntigenApoptosisCarcinogenesisCell DeathCell Line, TumorCell ProliferationCell SurvivalColonic NeoplasmsDrug Resistance, NeoplasmGene ExpressionGene Expression Regulation, NeoplasticHumansOncogene Protein v-aktPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionAC133 AntigenOncogene Protein v-aktPhosphatidylinositol 3-KinasesPROM1 protein, humanProto-Oncogene Proteins c-aktAktCD133colon carcinomaresistance to nutritional stress

Identifiers

PMID33720534
PMCPMC8091590
OpenAlexW3138488203

What OpenQuestion holds

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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.