Evidence map›Paper›PMID 29285156›Full record

ArticleExperimental and therapeutic medicine2017

Curcumin suppresses AGEs induced apoptosis in tubular epithelial cells via protective autophagy.

Ying Wei, Jiaqi Gao, Lingling Qin, Yunling Xu, Haoxia Shi, Lingxia Qu, Yongqiao Liu, Tunhai Xu, Tonghua Liu

Open access · diamondAbstract read
In one paragraph

Article in Experimental and therapeutic medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 39% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
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  6. Article
  7. Renoprotective Roles of Curcumin.Advances in experimental medicine and biology · 2021
    Article
  8. 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

9 authors at 1 institution in 1 country.

Ying WeiSchool of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing, Chaoyang 100102, P.R. China.
Jiaqi GaoSchool of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing, Chaoyang 100102, P.R. China.
Lingling QinHealth Cultivation Key Laboratory of The Ministry of Education, Beijing University of Chinese Medicine, Beijing, Chaoyang 100029, P.R. China.
Yunling XuSchool of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing, Chaoyang 100102, P.R. China.
Haoxia ShiSchool of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing, Chaoyang 100102, P.R. China.
Lingxia QuSchool of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing, Chaoyang 100102, P.R. China.
Yongqiao LiuSchool of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing, Chaoyang 100102, P.R. China.
Tunhai XuSchool of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing, Chaoyang 100102, P.R. China.
Tonghua LiuHealth Cultivation Key Laboratory of The Ministry of Education, Beijing University of Chinese Medicine, Beijing, Chaoyang 100029, P.R. China.
Beijing University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal tubular cell apoptosis and tubular dysfunction is an important process underlying diabetic nephropathy (DN). Understanding the mechanisms underlying renal tubular epithelial cell survival is important for the prevention of kidney damage associated with glucotoxicity. Curcumin has been demonstrated to possess potent anti-apoptotic properties. However, the roles of curcumin in renal epithelial cells are yet to be defined. The present study investigated advanced glycation or glycoxidation end-product (AGE)-induced toxicity in renal tubular epithelial cells via several complementary assays, including cell viability, cell apoptosis and cell autophagy in the NRK-52E rat kidney tubular epithelial cell line. The extent of apoptosis was significantly increased in the NRK-52E cells following treatment with AGEs. The results also indicated that curcumin reversed this effect by promoting autophagy through the phosphoinositide 3-kinase/AKT serine/threonine kinase signaling pathway. These conclusions suggested that curcumin exerts a renoprotective effect in the presence of AGEs, at least in part by activating autophagy in NRK-52E cells. Collectively, these findings indicate that curcumin not only exerts renoprotective effects, however may also act as a novel therapeutic strategy for the treatment of diabetic nephropathy.

Indexed as

AGEsapoptosisautophagycurcumindiabetic nephropathy

Identifiers

PMID29285156
PMCPMC5740722
OpenAlexW2765823213

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.