Evidence map›Paper›PMID 40124041›Full record

ArticleACS omega2025

Study on the Construction and Anti-Tumor Effect of aPDL1/aMUC1 Double Antibody Modification of Doxorubicin Liposome.

Shouzhen Zhao, Cuiling Xuan, Wenbin Diao, Ran Bai, Fei Wu, Wenjing Yu, Fan Yang, Jingliang Wu, Wei Xu, Guosheng Jiang and 2 more

Abstract read
In one paragraph

Article in ACS omega, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Shouzhen ZhaoSchool of Life Science and Technology, Shandong Second Medical University, Weifang 261053, Shandong, China.ORCID https://orcid.org/0000-0003-1215-8967
Cuiling XuanSchool of Life Science and Technology, Shandong Second Medical University, Weifang 261053, Shandong, China.
Wenbin DiaoClinical Laboratory, Second People's Hospital of Weifang, Weifang 261053, Shandong, China.
Ran BaiSchool of Life Science and Technology, Shandong Second Medical University, Weifang 261053, Shandong, China.
Fei WuSchool of Life Science and Technology, Shandong Second Medical University, Weifang 261053, Shandong, China.
Wenjing YuSchool of Life Science and Technology, Shandong Second Medical University, Weifang 261053, Shandong, China.
Fan YangShandong Kanghua Biotechnology Co., Ltd., Weifang 261053, Shandong, China.
Jingliang WuSchool of Life Science and Technology, Shandong Second Medical University, Weifang 261053, Shandong, China.ORCID https://orcid.org/0000-0001-6962-2842
Wei XuSchool of Life Science and Technology, Shandong Second Medical University, Weifang 261053, Shandong, China.
Guosheng JiangSchool of Life Science and Technology, Shandong Second Medical University, Weifang 261053, Shandong, China.
Zhiqin GaoSchool of Life Science and Technology, Shandong Second Medical University, Weifang 261053, Shandong, China.
Haimei LiSchool of Life Science and Technology, Shandong Second Medical University, Weifang 261053, Shandong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, the primary treatments for cancer have included chemotherapy, radiotherapy, and surgery. However, challenges such as poor prognosis, high recurrence rates, low survival rates, and diminished quality of life persist in cancer management. Recently, immunotherapy has emerged as a potent therapeutic approach for treating tumors. To this end, we developed antibodies for mucin 1 (MUC1) and programmed cell death ligand 1 (PD-L1) to functionalize liposomes and incorporate doxorubicin (DOX) (DOX-aMUC1/aPDL1-Lip). This formulation is designed to enhance its targeting capability and antitumor activity against cancer cells. The DOX-aMUC1/aPDL1-Lip formulation demonstrated significant antitumor effects both in vivo and in vitro, effectively inhibiting tumor cell growth. Utilizing antibodies against PD-L1 and MUC1 to modify liposomes represents a novel strategy for cancer treatment.

Identifiers

PMID40124041
PMCPMC11923672

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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.