Evidence map›Paper›PMID 36635685›Full record

ArticleBreast cancer research : BCR2023

MTX-PEG-modified CG/DMMA polymeric micelles for targeted delivery of doxorubicin to induce synergistic autophagic death against triple-negative breast cancer.

Zhiwen Cao, Rui Liu, Yang Li, Xinyi Luo, Zhenglai Hua, Xiangpeng Wang, Zeyu Xue, Zhengjia Zhang, Cheng Lu, Aiping Lu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

9 citing papers in PubMed, 24 citations in OpenAlex.

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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

11 authors at 3 institutions in 2 countries.

Zhiwen Cao *School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100029, China.
Rui Liu *School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100029, China.
Yang LiSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100029, China.
Xinyi LuoSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100029, China.
Zhenglai HuaSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100029, China.
Xiangpeng WangSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100029, China.
Zeyu XueSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100029, China.
Zhengjia ZhangSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100029, China.
Cheng LuInstitute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing, 100700, China. lv_cheng0816@163.com.
Aiping LuSchool of Chinese Medicine, Hong Kong Baptist University, Kowloon,, Hongkong, China. lap64067611@126.com.
Yuanyan LiuSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100029, China. yyliu_1980@163.com.
Beijing University of Chinese Medicine · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNHong Kong Baptist University · HK

Funding

Beijing Natural Science Foundation 7202111Innovation Team and Talents Cultivation Program of National Administration of Traditional Chinese Medicine ZYYCXTD-D-202005
6 · The paper itself

Abstract

The chemotherapy of triple-negative breast cancer based on doxorubicin (DOX) regimens suffers from great challenges on toxicity and autophagy raised off-target. In this study, a conjugate methotrexate-polyethylene glycol (shorten as MTX-PEG)-modified CG/DMMA polymeric micelles were prepared to endue DOX tumor selectivity and synergistic autophagic flux interference to reduce systematic toxicity and to improve anti-tumor capacity. The micelles could effectively promote the accumulation of autophagosomes in tumor cells and interfere with the degradation process of autophagic flux, collectively inducing autophagic death of tumor cells. In vivo and in vitro experiments showed that the micelles could exert improved anti-tumor effect and specificity, as well as reduced accumulation and damage of chemotherapeutic drugs in normal organs. The potential mechanism of synergistic autophagic death exerted by the synthesized micelles in MDA-MB-231 cells has been performed by autophagic flux-related pathway.

Indexed as

Breast NeoplasmsTriple Negative Breast NeoplasmsCell Line, TumorDoxorubicinFemaleHumansMaleic AnhydridesMethotrexateMicellesPolymers2,3-dimethylmaleic anhydrideDoxorubicinMaleic AnhydridesMethotrexateMicellesPolymersAutophagyChitosanDoxorubicinMicellesTriple-negative breast cancer

Identifiers

PMID36635685
PMCPMC9837947
OpenAlexW4315703326

What Socratic holds

Textmetadata
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 Socratic graph.