Evidence map›Paper›PMID 31192127›Full record

ArticleFrontiers in oncology2019

Aurora-A Induces Chemoresistance Through Activation of the AKT/mTOR Pathway in Endometrial Cancer.

Jun Wu, Ziyun Cheng, Xiaofeng Xu, Jian Fu, Kaiyue Wang, Tao Liu, Chan Wu, Xiangyi Kong, Qian Yang, Guijun Yan and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Endometrial Cancer Stem Cells: Where Do We Stand and Where Should We Go?International journal of molecular sciences · 2022
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. The role of Aurora-A in human cancers and future therapeutics.American journal of cancer research · 2020
    Review
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

11 authors at 2 institutions in 1 country.

Jun WuDepartment of Gynecology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.
Ziyun ChengDepartment of Gynecology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.
Xiaofeng XuDepartment of Gynecology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.
Jian FuDepartment of Gynecology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.
Kaiyue WangDepartment of Gynecology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.
Tao LiuDepartment of Gynecology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.
Chan WuDepartment of Gynecology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.
Xiangyi KongDepartment of Gynecology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.
Qian YangDepartment of Gynecology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.
Guijun YanReproductive Medicine Center, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.
Huaijun ZhouDepartment of Gynecology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.
Nanjing Drum Tower Hospital · CNThe First People's Hospital of Changzhou · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endometrial cancer (EC) is the most common gynecological tumor all over the world, and advanced/metastatic EC remains a malignancy with poor survival outcome due to highly resistant to conventional chemotherapeutic treatment. Here, we report that Aurora-A, a serine-threonine kinase, plays a vital role in chemoresistance of EC. Aurora-A is overexpressed in EC tissues, compared with normal endometrium and Aurora-A expression is associated with decreased overall survival. Overexpression of Aurora-A in EC cell lines (Ishikawa and HEC-1B cells) promotes cell proliferation and induced paclitaxel- and cisplatin-resistance. Furthermore, Aurora-A activating AKT-mTOR pathway further induces chemoresistance

Indexed as

AKT signalingAurora-AChemoresistanceEndometrial cancermTOR signaling

Identifiers

PMID31192127
PMCPMC6540875
OpenAlexW2945977427

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.