Evidence map›Paper›PMID 41560835›Full record

ReviewMaterials today. Bio2026

Aptamer-liposome targeted nanotherapeutics for cancer therapy: Bibliometric analysis, recent developments and future perspectives.

Zhao Gao, Sang Du, Jiarui Song, Yating Gao, Xin Peng, Xin Lin, Shuang E, Yinan Zhao, Shubiao Zhang

Abstract readReview
In one paragraph

Review in Materials today. Bio, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Biomimetic Scaffold-Based 3D Models for Decoding Cancer Biology and Advancing Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  2. Aptamers in cancer therapy: Why has clinical translation lagged behind preclinical promise?Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2026
    Review
  3. 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

9 authors.

Zhao GaoKey Laboratory of Biotechnology and Bioresources Utilization of Ministry of Education, School of Life Science, Dalian Minzu University, Dalian, 116600, Liaoning, China.
Sang DuKey Laboratory of Biotechnology and Bioresources Utilization of Ministry of Education, School of Life Science, Dalian Minzu University, Dalian, 116600, Liaoning, China.
Jiarui SongKey Laboratory of Biotechnology and Bioresources Utilization of Ministry of Education, School of Life Science, Dalian Minzu University, Dalian, 116600, Liaoning, China.
Yating GaoKey Laboratory of Biotechnology and Bioresources Utilization of Ministry of Education, School of Life Science, Dalian Minzu University, Dalian, 116600, Liaoning, China.
Xin PengSchool of Life Sciences, Tianjin University, Tianjin, 300072, China.
Xin LinCollege of Chemistry and Chemical Engineering, Liaoning Normal University, Dalian, 116029, Liaoning, China.
Shuang EKey Laboratory of Biotechnology and Bioresources Utilization of Ministry of Education, School of Life Science, Dalian Minzu University, Dalian, 116600, Liaoning, China.
Yinan ZhaoKey Laboratory of Biotechnology and Bioresources Utilization of Ministry of Education, School of Life Science, Dalian Minzu University, Dalian, 116600, Liaoning, China.
Shubiao ZhangKey Laboratory of Biotechnology and Bioresources Utilization of Ministry of Education, School of Life Science, Dalian Minzu University, Dalian, 116600, Liaoning, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As one of the leading causes of death worldwide, cancer has driven the advancement of targeted therapy toward greater precision and reduced off-target effects. Liposomes, with their biocompatibility, tunable properties, and clinical success, are among the most promising nanocarriers, yet their tumor-targeting specificity remains limited. Aptamer-functionalized liposomes provide a synergistic solution by combining selective aptamer-receptor recognition with efficient drug encapsulation, achieving enhanced tumor targeting and controlled release. Recent advances have expanded this platform toward multi-targeting, stimuli-responsive systems, and theranostic applications, thereby extending the potential of conventional liposomes. This review offers an integrated perspective on the structural design, internalization pathways, and therapeutic applications of aptamer-liposome systems across various cancers. Key barriers, including aptamer instability, scalable conjugation, and limited clinical translation, are critically discussed, alongside emerging strategies to address them. The convergence of aptamer targeting and liposomal delivery represents a transformative step toward next-generation nanotherapeutics, offering a paradigm shift in precision oncology by enabling personalized, selective, and multifunctional cancer therapy.

Indexed as

AptamerCancer therapyLiposomeTargeted drug delivery

Identifiers

PMID41560835
PMCPMC12814084

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.