Evidence map›Paper›PMID 38913037›Full record

ArticleAging and disease2024

Treatment of Rheumatoid Arthritis Based on the Inherent Bioactivity of Black Phosphorus Nanosheets.

Cheng Zhuang, Ruiqi Sun, Yuchen Zhang, Qing Zou, Jianxin Zhou, Naijun Dong, Xuyu Zhao, Wenjun Fu, Xiaoke Geng, Jiao Wang and 2 more

Abstract read
In one paragraph

Article in Aging and disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
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  6. 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

12 authors.

Cheng ZhuangSchool of Life Sciences, Shanghai University, Shanghai, China.
Ruiqi SunSchool of Life Sciences, Shanghai University, Shanghai, China.
Yuchen ZhangSchool of Medicine, Shanghai University, Shanghai, China.
Qing ZouSchool of Life Sciences, Shanghai University, Shanghai, China.
Jianxin ZhouSchool of Life Sciences, Shanghai University, Shanghai, China.
Naijun DongSchool of Life Sciences, Shanghai University, Shanghai, China.
Xuyu ZhaoSchool of Life Sciences, Shanghai University, Shanghai, China.
Wenjun FuSchool of Life Sciences, Shanghai University, Shanghai, China.
Xiaoke GengSchool of Life Sciences, Shanghai University, Shanghai, China.
Jiao WangSchool of Life Sciences, Shanghai University, Shanghai, China.
Qian LiInstitute of Basic Medical Sciences Chinese Academy of Medical Sciences, School of Basic Medicine Peking Union Medical College, Beijing, China.
Robert Chunhua ZhaoSchool of Life Sciences, Shanghai University, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rheumatoid arthritis (RA) is an autoimmune disease that affects the living quality of patients, especially the elderly population. RA-related morbidity and mortality increase significantly with age, while current clinical drugs for RA are far from satisfactory and may have serious side effects. Therefore, the development of new drugs with higher biosafety and efficacy is demanding. Black phosphorus nanosheets (BPNSs) have been widely studied because of their excellent biocompatibility. Here, we focus on the inherent bioactivity of BPNSs, report the potential of BPNSs as a therapeutic drug for RA and elucidate the underlying therapeutic mechanism. We find that BPNSs inhibit autophagy at an early stage via the AMPK-mTOR pathway, switch the energy metabolic pathway to oxidative phosphorylation, increase intracellular ATP levels, suppress apoptosis, reduce inflammation and oxidative stress, and down-regulate senescence-associated secretory phenotype (SASP)-related genes in rheumatoid arthritis synovial fibroblasts (RA-SFs). Further, BPNSs induce the apoptosis of macrophages and promote their transition from the M1 to the M2 phenotype by regulating related cytokines. Significantly, the administration of BPNSs can alleviate key pathological features of RA in mice, revealing great therapeutic potential. This study provides a novel option for treating RA, with BPNSs emerging as a promising therapeutic candidate.

Indexed as

Arthritis, RheumatoidNanostructuresPhosphorusAnimalsApoptosisAutophagyFibroblastsHumansMacrophagesMiceOxidative StressSynovial MembranePhosphorus

Identifiers

PMID38913037
PMCPMC12096912

What OpenQuestion holds

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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.