Evidence map›Paper›PMID 24755555›Full record

ArticleBMB reports2015

Upregulation of Fas in epithelial ovarian cancer reverses the development of resistance to cisplatin.

Fan Yang, Wang Long, Han Xuechuan, Liu Xueqin, Ma Hongyun, Ding Yonghui

Open access · goldAbstract read
In one paragraph

Article in BMB reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

10 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Role of Epigenetics for the Efficacy of Cisplatin.International journal of molecular sciences · 2024
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Loss of α(E)-catenin promotes Fas mediated apoptosis in tubular epithelial cells.Apoptosis : an international journal on programmed cell death · 2015
    Article
  10. MCT1 promotes the cisplatin-resistance by antagonizing Fas in epithelial ovarian cancer.International journal of clinical and experimental pathology · 2015
    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

6 authors at 2 institutions in 1 country.

Fan YangDepartment of Obstetrics and Gynecology, Ningxia People's Hospital, Yinchuan 750002, People's Republic of China.
Wang LongNingxia Medical University, Yinchuan 750004, People's Republic of China.
Han XuechuanDepartment of Obstetrics and Gynecology, Ningxia People's Hospital, Yinchuan 750002, People's Republic of China.
Liu XueqinDepartment of Obstetrics and Gynecology, Ningxia People's Hospital, Yinchuan 750002, People's Republic of China.
Ma HongyunDepartment of Obstetrics and Gynecology, Ningxia People's Hospital, Yinchuan 750002, People's Republic of China.
Ding YonghuiAffiliated Hospital of Ningxia Medical University, Yinchuan 750004, People's Republic of China.
Ningxia Hui Autonomous Region Peoples Hospital · CNNingxia Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study was to investigate the role of Fas in the development of Cisplatin-resistant ovarian cancer. On the cellular level, Fas expression was significantly reduced in Cisplatin resistant A2780 (A2780/CP) cells compared with A2780 cells. Fas silence with siRNA would promote tumor cell lines proliferation, facilitate tumor cell cycle transition of G1/S, prevent cell apoptosis, and promote cell migration. Expression of drug resistance gene was negatively correlated to Fas. In nude mice metastasis model of human ovarian carcinoma by subcutaneous transplantation, after Ad-Fas injected intratumorly, we found that upregulation of Fas could inhibit transplantation tumor tissue growth and reduce the expression of drug resistance gene. Our results indicated that upregulation of Fas in epithelial ovarian cancer reversed the development of resistance to Cisplatin. In conclusion, our findings suggested that Fas might act as a promising therapeutic target for improvement of the sensibility to Cisplatin in ovarian cancer.

Indexed as

AnimalsAntineoplastic AgentsApoptosisATP-Binding Cassette, Sub-Family C ProteinsATP Binding Cassette Transporter, Subfamily B, Member 1Cell Line, TumorCell MovementCisplatinDrug Resistance, Neoplasmfas ReceptorFemaleG1 Phase Cell Cycle CheckpointsHumansMajor Vault ProteinMiceMice, NudeAntineoplastic AgentsATP-Binding Cassette, Sub-Family C ProteinsATP Binding Cassette Transporter, Subfamily B, Member 1CisplatinFAS protein, humanfas ReceptorMajor Vault ProteinMultidrug Resistance-Associated Protein 2RNA, Small InterferingVault Ribonucleoprotein Particles

Identifiers

PMID24755555
PMCPMC4345639
OpenAlexW2093988119

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.