Evidence map›Paper›PMID 38553451›Full record

ArticleNature communications2024

Nanoparticles targeting mutant p53 overcome chemoresistance and tumor recurrence in non-small cell lung cancer.

Yu-Yang Bi, Qiu Chen, Ming-Yuan Yang, Lei Xing, Hu-Lin Jiang

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
11.9field-weighted citation impact, top 1% 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

49 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Genetic insights into lung squamous cell carcinoma: howTranslational cancer research · 2026
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  12. Identification and experimental verification of a novel cisplatin resistance-related lncRNA signature for predicting prognosis and immune response in lung adenocarcinoma.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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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

5 authors at 1 institution in 1 country.

Yu-Yang BiState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, 210009, China.
Qiu ChenState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, 210009, China.
Ming-Yuan YangState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, 210009, China.
Lei XingState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, 210009, China.
Hu-Lin JiangState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, 210009, China. jianghulin3@gmail.com.ORCID http://orcid.org/0000-0002-1620-1777
China Pharmaceutical University · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82020108029National Natural Science Foundation of China (National Science Foundation of China) 82073398
6 · The paper itself

Abstract

Non-small cell lung cancer (NSCLC) shows high drug resistance and leads to low survival due to the high level of mutated Tumor Protein p53 (TP53). Cisplatin is a first-line treatment option for NSCLC, and the p53 mutation is a major factor in chemoresistance. We demonstrate that cisplatin chemotherapy increases the risk of TP53 mutations, further contributing to cisplatin resistance. Encouragingly, we find that the combination of cisplatin and fluvastatin can alleviate this problem. Therefore, we synthesize Fluplatin, a prodrug consisting of cisplatin and fluvastatin. Then, Fluplatin self-assembles and is further encapsulated with poly-(ethylene glycol)-phosphoethanolamine (PEG-PE), we obtain Fluplatin@PEG-PE nanoparticles (FP NPs). FP NPs can degrade mutant p53 (mutp53) and efficiently trigger endoplasmic reticulum stress (ERS). In this study, we show that FP NPs relieve the inhibition of cisplatin chemotherapy caused by mutp53, exhibiting highly effective tumor suppression and improving the poor NSCLC prognosis.

Indexed as

Antineoplastic AgentsCarcinoma, Non-Small-Cell LungLung NeoplasmsNanoparticlesPhosphatidylethanolaminesPolyethylene GlycolsCell Line, TumorCisplatinDrug Resistance, NeoplasmFluvastatinHumansMutationNeoplasm Recurrence, LocalTumor Suppressor Protein p53Antineoplastic AgentsCisplatindioleoyl-N-(monomethoxypolyethylene glycol succinyl)phosphatidylethanolamineFluvastatinPhosphatidylethanolaminesPolyethylene GlycolsTumor Suppressor Protein p53

Identifiers

PMID38553451
PMCPMC10980692
OpenAlexW4393305640

What OpenQuestion holds

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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.