Evidence map›Paper›PMID 36135176›Full record

ArticleCurrent issues in molecular biology2022

(-)-Xanthatin as a Killer of Human Breast Cancer MCF-7 Mammosphere Cells: A Comparative Study with Salinomycin.

Shuso Takeda, Masayo Hirao-Suzuki, Mitsuru Shindo, Hironori Aramaki

Open access · goldAbstract read
In one paragraph

Article in Current issues in molecular biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 43% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. International journal of molecular sciences · 2023
    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

4 authors at 4 institutions in 1 country.

Shuso TakedaLaboratory of Molecular Life Sciences, Faculty of Pharmacy and Pharmaceutical Sciences, Fukuyama University, Sanzou 1, Hiroshima 729-0292, Japan.ORCID 0000-0003-2193-1421
Masayo Hirao-SuzukiLaboratory of Xenobiotic Metabolism and Environmental Toxicology, Faculty of Pharmaceutical Sciences, Hiroshima International University, 5-1-1 Hiro-koshingai, Hiroshima 737-0112, Japan.ORCID 0000-0002-5626-1950
Mitsuru ShindoInstitute for Materials Chemistry and Engineering, Kyushu University, 6-1 Kasuga-koen, Kasuga 816-8580, Japan.ORCID 0000-0002-0588-8075
Hironori AramakiDepartment of Molecular Biology, Daiichi University of Pharmacy, 22-1 Tamagawa-cho, Fukuoka 815-8511, Japan.ORCID 0000-0003-0499-0868
Daiichi University of Pharmacy · JPFukuyama University · JPHiroshima International University · JPKyushu University · JP

Funding

Cooperative Research Program of the Network Joint Research Center for Materials and Devices 2012320Cooperative Research Program of the Network Joint Research Center for Materials and Devices 2013373Cooperative Research Program of the Network Joint Research Center for Materials and Devices 20163071Cooperative Research Program of the Network Joint Research Center for Materials and Devices 20211327Cooperative Research Program of the Network Joint Research Center for Materials and Devices 20221077Japan Society for the Promotion of Science 17K08402Japan Society for the Promotion of Science 21K12261Japan Society for the Promotion of Science 22H02744Japan Society for the Promotion of Science 22K15288Research Foundation for Pharmaceutical Sciences NonScience and Technology Research Promotion Program for Agriculture, Forestry, Fisheries and Food industry Non
6 · The paper itself

Abstract

Experimental evidence accumulated by our research group and others strongly suggests that (-)-xanthatin, a xanthanolide sesquiterpene lactone, exhibits anti-proliferative effects on human breast cancer cells (in vitro) as well as anti-tumor effects in experimental animals (in vivo). In cancer biology, it is now critically important for anti-cancer agents to selectively target cancer stem cells (CSCs) in order to overcome cancer therapeutic resistance and recurrence. However, it has not yet been established whether (-)-xanthatin abrogates the formation of breast CSCs. In the present study, we utilized chemically synthesized pure (-)-xanthatin and a culture system to obtain mammospheres from human breast cancer MCF-7 cells, which are a CSC-enriched population. We herein demonstrated for the first time that (-)-xanthatin exhibited the ability to kill mammospheres, similar to salinomycin, an established selective killer of CSCs. A possible anti-proliferative mechanism toward mammospheres by (-)-xanthatin is discussed.

Indexed as

cancer stem cellsGADD45GmammospheresMCF-7 cells(–)-xanthatin

Identifiers

PMID36135176
PMCPMC9497939
OpenAlexW4293103707

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.