Evidence map›Paper›PMID 36405550›Full record

ArticleActa histochemica et cytochemica2022

Role of Cancer Stem-like Cells in the Process of Invasion and Mesenchymal Transformation by a Reconstituted Triple-negative Breast Cancer Cell Population Resistant to p53-induced Apoptosis.

Sana Inoue, Miki Imanishi, Ai Kanzaki, Atsumi Fujimoto, Marina Maeyama, Ayaka Okamoto, Hiroka Matsuda, Kiyotsugu Yoshikawa, Rei Takahashi

Open access · diamondAbstract read
In one paragraph

Article in Acta histochemica et cytochemica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. 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 1 institution in 1 country.

Sana InoueGraduate School of Pharmaceutical Sciences Doshisha Women's College of Liberal Arts, Kyoto, Japan.
Miki ImanishiFaculty of Pharmaceutical Sciences Doshisha Women's College of Liberal Arts, Kyoto, Japan.
Ai KanzakiFaculty of Pharmaceutical Sciences Doshisha Women's College of Liberal Arts, Kyoto, Japan.
Atsumi FujimotoFaculty of Pharmaceutical Sciences Doshisha Women's College of Liberal Arts, Kyoto, Japan.
Marina MaeyamaFaculty of Pharmaceutical Sciences Doshisha Women's College of Liberal Arts, Kyoto, Japan.
Ayaka OkamotoFaculty of Pharmaceutical Sciences Doshisha Women's College of Liberal Arts, Kyoto, Japan.
Hiroka MatsudaFaculty of Pharmaceutical Sciences Doshisha Women's College of Liberal Arts, Kyoto, Japan.
Kiyotsugu YoshikawaFaculty of Pharmaceutical Sciences Doshisha Women's College of Liberal Arts, Kyoto, Japan.
Rei TakahashiGraduate School of Pharmaceutical Sciences Doshisha Women's College of Liberal Arts, Kyoto, Japan.
Doshisha Women's College of Liberal Arts · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We investigated the role of cancer stem cells (CSCs) in a population of triple-negative breast cancer (TNBC) cells that are resistant to apoptosis. A human breast cancer cell population capable of inducing p53 expression with doxycycline (Dox) was created and used as an untreated control (UT). After the addition of Dox to UT for 5 days, the cell population reconstituted with cells showing resistance to apoptosis was named RE. Fluorescence-activated cell sorting (FACS) and immunostaining revealed that after the addition of Dox, the ratio of cells in the S and G2/M phases decreased in UT as apoptosis proceeded, but did not markedly change in apoptosis-resistant RE. CSC-like cells in RE exhibited a cell morphology with a larger ratio of the major/minor axis than UT. FACS showed that RE had a higher proportion of CSC-like cells and contained more CD44

Indexed as

apoptosis resistancebreast cancercancer stem-like cellinvasion

Identifiers

PMID36405550
PMCPMC9631983
OpenAlexW4308001638

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.