Evidence map›Paper›PMID 34992692›Full record

ArticleOncology letters2022

Discovering novel mechanisms of taxane resistance in human breast cancer by whole-exome sequencing.

Yumi Wanifuchi-Endo, Naoto Kondo, Yu Dong, Takashi Fujita, Tomoko Asano, Tomoka Hisada, Yasuaki Uemoto, Sayaka Nishikawa, Yusuke Katagiri, Akiko Kato and 6 more

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 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
0.1field-weighted citation impact, top 54% 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, 2 citations in OpenAlex.

  1. Review
  2. Pentagamavunone-1 inhibits aggressive breast cancer cell proliferation through mitotic catastrophe and ROS-mediated activities:Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2024
    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

16 authors at 1 institution in 1 country.

Yumi Wanifuchi-EndoDepartment of Breast Surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Naoto KondoDepartment of Breast Surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Yu DongDepartment of Breast Surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Takashi FujitaDepartment of Breast Surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Tomoko AsanoDepartment of Breast Surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Tomoka HisadaDepartment of Breast Surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Yasuaki UemotoDepartment of Breast Surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Sayaka NishikawaDepartment of Breast Surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Yusuke KatagiriDepartment of Breast Surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Akiko KatoDepartment of Breast Surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Mitsuo TeradaDepartment of Breast Surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Hiroshi SugiuraEducation and Research Center for Advanced Medicine, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Katsuhiro OkudaDepartment of Oncology, Immunology and Surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Hiroyuki KatoDepartment of Experimental Pathology and Tumor Biology, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Satoru TakahashiDepartment of Experimental Pathology and Tumor Biology, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Tatsuya ToyamaDepartment of Breast Surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
Nagoya City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Taxanes are important drugs used in the treatment of breast cancer; however, some cancer types are taxane-resistant. The aim of the present study was to investigate the underlying mechanisms of taxane resistance using whole-exome sequencing (WES). Six patients with breast cancer whose tumors responded well to anthracycline treatment but grew rapidly during neoadjuvant taxane-based chemotherapy, were included in the present study. WES of samples from these patients was carried out to identify somatic mutations of candidate genes thought to affect taxane resistance, and the candidate proteins were structurally modeled. The mRNA and protein expression levels of these candidate genes in other breast cancers treated with taxanes were also examined. Nine variants common to all six patients were identified and two of these [R552P in V-type proton ATPase catalytic subunit A (

Indexed as

APOBEC3FATP6V1Abreast cancertaxane resistance

Identifiers

PMID34992692
PMCPMC8721851
OpenAlexW4200007798

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.