Evidence map›Paper›PMID 35140705›Full record

ArticleFrontiers in immunology2021

Everolimus Alleviates Renal Allograft Interstitial Fibrosis by Inhibiting Epithelial-to-Mesenchymal Transition Not Only

Zeping Gui, Chuanjian Suo, Jun Tao, Zijie Wang, Ming Zheng, Shuang Fei, Hao Chen, Li Sun, Zhijian Han, Xiaobing Ju and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Cystinosis and Cellular Energy Failure: Mitochondria at the Crossroads.International journal of molecular sciences · 2026
    Review
  3. Review
  4. Advances in microfluidic chip technology for cell analysis.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2025
    Review
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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

13 authors at 3 institutions in 2 countries.

Zeping GuiDepartment of Urology, the Second Affiliated Hospital With Nanjing Medical University, Nanjing, China.
Chuanjian SuoDepartment of Urology, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.
Jun TaoDepartment of Urology, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.
Zijie WangDepartment of Urology, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.
Ming ZhengDepartment of Urology, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.
Shuang FeiDepartment of Urology, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.
Hao ChenDepartment of Urology, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.
Li SunDepartment of Urology, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.
Zhijian HanDepartment of Urology, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.
Xiaobing JuDepartment of Urology, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.
Hengcheng ZhangTransplantation Research Center, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.
Min GuDepartment of Urology, the Second Affiliated Hospital With Nanjing Medical University, Nanjing, China.
Ruoyun TanDepartment of Urology, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.
Nanjing Medical University · CNHarvard University · USSecond Affiliated Hospital of Nanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic allograft dysfunction (CAD) is the major cause of late graft loss in long-term renal transplantation. In our previous study, we found that epithelial-mesenchymal transition (EMT) is a significant event in the progression of renal allograft tubulointerstitial fibrosis, and impaired autophagic flux plays a critical role in renal allograft fibrosis. Everolimus (EVR) has been reported to be widely used to prevent the progression of organ fibrosis and graft rejection. However, the pharmacological mechanism of EVR in kidney transplantation remains to be determined. We used CAD rat model and the human kidney 2 (HK2) cell line treated with tumor necrosis factor-α (TNF-α) and EVR to examine the role of EVR on TNF-α-induced EMT and transplanted renal interstitial fibrosis. Here, we found that EVR could attenuate the progression of EMT and renal allograft interstitial fibrosis, and also activate autophagy

Indexed as

AnimalsAutophagyCells, CulturedEpithelial-Mesenchymal TransitionEverolimusFibrosisGraft RejectionKidneyKidney DiseasesKidney TransplantationNF-kappa BNF-KappaB Inhibitor alphaRatsRats, Inbred F344Signal TransductionTransplantation, HomologousEverolimusNF-kappa BNF-KappaB Inhibitor alphaautophagychronic renal graft dysfunctionEMTeverolimusrenal allograft interstitial fibrosis

Identifiers

PMID35140705
PMCPMC8818677
OpenAlexW4207023698

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.