Evidence map›Paper›PMID 39188744›Full record

ArticleSmart medicine2022

Reregulated mitochondrial dysfunction reverses cisplatin resistance microenvironment in colorectal cancer.

Yonghui Wang, Xiaodong Ma, Wenhui Zhou, Chang Liu, Hongbo Zhang

Erratum issuedAbstract read
In one paragraph

Article in Smart medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

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  4. IGLC3Frontiers in immunology · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Yonghui WangPharmaceutical Sciences Laboratory Åbo Akademi University Turku Finland.
Xiaodong MaPharmaceutical Sciences Laboratory Åbo Akademi University Turku Finland.
Wenhui ZhouPharmaceutical Sciences Laboratory Åbo Akademi University Turku Finland.
Chang LiuPharmaceutical Sciences Laboratory Åbo Akademi University Turku Finland.
Hongbo ZhangPharmaceutical Sciences Laboratory Åbo Akademi University Turku Finland.ORCID https://orcid.org/0000-0002-1071-4416

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemotherapy is one of the most basic and important treatments for malignant tumors. However, most chemotherapeutic drugs suffer from the resistance of tumor cells and lead to chemotherapy failure. Multidrug resistance (MDR) of tumor cells is the main obstacle to chemotherapy failure. The generation of MDR is not only the result of the performance of tumor cells, but the tumor microenvironment (TEM) also plays an important role in this process. The simultaneous dual intervention of cancer cells and the TEM has the potential to provide surprising results in overcoming MDR tumor therapy. Therefore, in this study, we designed a folate acid ligand-modified nanoparticle (FA-NPs) with a size of about 145 nm targeting multidrug-resistant colorectal cancer and successfully co-loaded cisplatin and Tris(2-chloroisopropyl) phosphate (TCPP). FA-NPs can enrich tumor sites through receptor-mediated endocytosis. In vitro mechanism studies have shown that nanoparticles can reverse cisplatin resistance mainly by further increasing the level of reactive oxygen species in tumor cells, breaking the homeostasis of the internal environment, then trigging mitochondrial stress, regulating drug resistance-related pathways, and improving the tumor drug resistance microenvironment; finally, the cisplatin recovers the antitumor effect with assistance from TCPP.

Indexed as

biomimetic drug deliverycolorectal cancermitochondrial regulationMSN‐based nanoparticlesmultidrug resistance

Identifiers

PMID39188744
PMCPMC11235731

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.