Evidence map›Paper›PMID 39165377›Full record

ReviewFrontiers in medicine2024

PTEN in kidney diseases: a potential therapeutic target in preventing AKI-to-CKD transition.

Fangfang Cao, Yuanyuan Li, Ting Peng, Yuanmei Li, Lihua Yang, Lanping Hu, Han Zhang, Jiali Wang

Abstract readReview
In one paragraph

Review in Frontiers in medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. 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

8 authors.

Fangfang Cao *Division of Nephrology, Mianyang Central Hospital, Mianyang, China.
Yuanyuan Li *Division of Science and Education, Mianyang Central Hospital, Mianyang, China.
Ting PengDivision of Nephrology, Mianyang Central Hospital, Mianyang, China.
Yuanmei LiDivision of Nephrology, Mianyang Central Hospital, Mianyang, China.
Lihua YangDivision of Nephrology, Mianyang Central Hospital, Mianyang, China.
Lanping HuHemodialysis Center, Mianyang Central Hospital, Mianyang, Sichuan, China.
Han ZhangHemodialysis Center, Mianyang Central Hospital, Mianyang, Sichuan, China.
Jiali WangDivision of Nephrology, Mianyang Central Hospital, Mianyang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal fibrosis, a critical factor in the development of chronic kidney disease (CKD), is predominantly initiated by acute kidney injury (AKI) and subsequent maladaptive repair resulting from pharmacological or pathological stimuli. Phosphatase and tensin homolog (PTEN), also known as phosphatase and tensin-associated phosphatase, plays a pivotal role in regulating the physiological behavior of renal tubular epithelial cells, glomeruli, and renal interstitial cells, thereby preserving the homeostasis of renal structure and function. It significantly impacts cell proliferation, apoptosis, fibrosis, and mitochondrial energy metabolism during AKI-to-CKD transition. Despite gradual elucidation of PTEN's involvement in various kidney injuries, its specific role in AKI and maladaptive repair after injury remains unclear. This review endeavors to delineate the multifaceted role of PTEN in renal pathology during AKI and CKD progression along with its underlying mechanisms, emphasizing its influence on oxidative stress, autophagy, non-coding RNA-mediated recruitment and activation of immune cells as well as renal fibrosis. Furthermore, we summarize prospective therapeutic targeting strategies for AKI and CKD-treatment related diseases through modulation of PTEN.

Indexed as

AKIAKI-to-CKDCKDkidneyPTEN

Identifiers

PMID39165377
PMCPMC11333338

What OpenQuestion holds

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Registered trials

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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.