Evidence map›Paper›PMID 28386373›Full record

ArticleAmerican journal of translational research2017

Mechanism of progestin resistance in endometrial precancer/cancer through Nrf2-survivin pathway.

Rujia Fan, Yiying Wang, Yue Wang, Li Wei, Wenxin Zheng

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2017. 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
0.8field-weighted citation impact, top 29% 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, 22 citations in OpenAlex.

  1. Review
  2. Review
  3. Phosphorylation of IDH1 Facilitates Progestin Resistance in Endometrial Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Brusatol: A potential anti-tumor quassinoid fromChinese herbal medicines · 2020
    Review
  10. Article
  11. 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

5 authors at 2 institutions in 2 countries.

Rujia FanDepartment of Obstetrics and Gynecology, Henan Province People's HospitalZhengzhou, China; Department of Obstetrics and Gynecology, Zhengzhou University People's HospitalZhengzhou, China.
Yiying WangDepartment of Obstetrics and Gynecology, Henan Province People's HospitalZhengzhou, China; Department of Obstetrics and Gynecology, Zhengzhou University People's HospitalZhengzhou, China.
Yue WangDepartment of Obstetrics and Gynecology, Henan Province People's HospitalZhengzhou, China; Department of Obstetrics and Gynecology, Zhengzhou University People's HospitalZhengzhou, China.
Li WeiDepartment of Obstetrics and Gynecology, Henan Province People's HospitalZhengzhou, China; Department of Obstetrics and Gynecology, Zhengzhou University People's HospitalZhengzhou, China.
Wenxin ZhengDepartment of Pathology, University of Texas Southwestern Medical CenterDallas, TX, USA; Department of Obstetrics and Gynecology, University of Texas Southwestern Medical CenterDallas, TX, USA; Department of Harold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical CenterDallas, TX, USA.
Zhengzhou University · CNThe University of Texas Southwestern Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Progestin is commonly used for young patients suffering from endometrial hyperplasia or cancer. However, there is approximately 30% failure rate with unclear mechanism. We investigated if Nrf2-survivin pathway contributes the progestin resistance (PR) in this setting. Current study detected Nrf2 and survivin protein expression in post progestin treated endometrial tissue samples by using immunohistochemistry. Transfection of Nrf2 and survivin into endometrial cancer cells in vitro was done to determine the roles of Nrf2 and survivin in progestin resistance. Silence of survivin was then performed to explore if Nrf2-driven progestin resistance is mediated by survivin. Medorxyprogesterone acetate (MPA) and metformin were applied to examine the cellular proliferations under the controlled conditions. Overexpression of survivin and Nrf2 were found in progestin-resistant endometrial samples as well as in those areas with only partial responses after MPA treatment. In contrast, all responded endometrial tissue with complete decidualization showed negative expression of these two biomarkers. Exogenous overexpression of Nrf2 and survivin resulted in progestin resistance. In addition, reduction of survivin in endometrial cancer cells overcame the Nrf2 overexpression induced progestin resistance. Furthermore, Nrf2 and survivin expressions were effectively suppressed after withdrawal of MPA. Interestingly, metformin increased the progestin sensitivity by down regulation of Nrf2 and survivin. The findings suggest that dysregulation of Nrf2-survivin may represent part of the molecular mechanisms of progestin resistance in endometrial cancer. Detecting survivin and Nrf2 may predict progestin resistance, while targeting Nrf2 and survivin may represent a promising prevention and treatment strategy for endometrial cancer.

Indexed as

Endometrial cancerendometrial hyperplasiaendometrial precancerNrf2progestin resistancesurvivin

Identifiers

PMID28386373
PMCPMC5376038
OpenAlexW2613692785

What OpenQuestion holds

Textmetadata
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.