Evidence map›Paper›PMID 37933642›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2023

[Liposome nanoparticles for targeted delivery of parthenolide induce colorectal cancer necroptosis to ameliorate tumor-infiltrating T cell exhaustion in mice].

W Yao, X Wang, Y Yang, J You, J Jin, P Zeng, Q Han, X Yao, X Sun, J Zhou

Open access · greenAbstract readEnglish Abstract
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. 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

10 authors at 3 institutions in 1 country.

W YaoLaboratory of Molecular Medicine, School of Traditional Chinese Medicine, Southern Medical University, Guangzhou 510515, China.
X WangGuangdong Provincial Key Laboratory of Construction and Detection in Tissue Engineering, School of Biomedical Engineering, Southern Medical University, Guangzhou 510515, China.
Y YangLaboratory of Molecular Medicine, School of Traditional Chinese Medicine, Southern Medical University, Guangzhou 510515, China.
J YouLaboratory of Molecular Medicine, School of Traditional Chinese Medicine, Southern Medical University, Guangzhou 510515, China.
J JinGuangdong Provincial People's Hospital, Guangzhou 519041, China.
P ZengGuangdong Provincial People's Hospital, Guangzhou 519041, China.
Q HanLaboratory of Molecular Medicine, School of Traditional Chinese Medicine, Southern Medical University, Guangzhou 510515, China.
X YaoGuangdong Provincial People's Hospital, Guangzhou 519041, China.
X SunLaboratory of Molecular Medicine, School of Traditional Chinese Medicine, Southern Medical University, Guangzhou 510515, China.
J ZhouHospital of Integrated Traditional Chinese and Western Medicine, Southern Medical University, Guangzhou 510315, China.
TCM-Intigrated Cancer Center of Southern Medical University · CNGuangdong Provincial People's Hospital · CNSouthern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the mechanism of parthenolide for inducing necroptosis and ameliorating CD8

methodsThe inhibitory effect of parthenolide on proliferation of different CRC cell lines was examined using CCK8 assay, and ROS LDH detection and Western blotting were used to analyze the cell death pathways. In a mouse model bearing subcutaneous MC38 cell xenografts, the effects of 5 and 15 mg/kg parthenolide on tumor growth and CD8

resultsTreatment with parthenolide dose-dependently lowered the viability of the CRC cell lines SW480, DLD1, HCT116 and MC38 cells, and its effect was obviously antagonized by Nec-1. Immunoblotting analysis showed that parthenolide treatment resulted in increased RIP3 and MLKL phosphorylation in the CRC cells. In the mouse model bearing subcutaneous xenografts, parthenolide treatment at the high dose, but not at the low dose, significantly increased the number of infiltrating CD3

conclusionParthenolide induces necroptosis in CRC and increases infiltrating CD8

Indexed as

Colorectal NeoplasmsNanoparticlesAnimalsCD8-Positive T-LymphocytesHepatitis A Virus Cellular Receptor 2HumansLiposomesMiceNecroptosisSesquiterpenesT-Cell ExhaustionHepatitis A Virus Cellular Receptor 2LiposomesparthenolideSesquiterpenescolorectal cancernanoparticlesnecroptosisparthenolideT cell exhaustion

Identifiers

PMID37933642
PMCPMC10630204
OpenAlexW4388466197

What OpenQuestion holds

Textmetadata
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.