Evidence map›Paper›PMID 41024179›Full record

ReviewJournal of nanobiotechnology2025

Engineered exosomes: a promising approach for overcoming challenges in pancreatic cancer therapy.

Mo Sha, Yang Gao, Xu Yin, Xueyao Li, Caiqi Liu, Shuang Li

Registry-linked trialAbstract readReview
In one paragraph

Review in Journal of nanobiotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07226154 (An Exosomal miRNA Based Predictive Model for Personalized Neoadjuvant Chemotherapy Selection in Pancreatic Ductal Adenocarcinoma), which is not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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.

NCT07226154 recruitingnot on this map

An Exosomal miRNA Based Predictive Model for Personalized Neoadjuvant Chemotherapy Selection in Pancreatic Ductal Adenocarcinoma

TypeobservationalSponsorCity of Hope Medical CenterRan2024 to 2026Enrolled200ConditionsPancreatic Ductal AdenocarcinomaArmsSmall RNA sequencing, PRECEPT assay (qRT-PCR validation)
3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. HMTA, a natural alkylphenol fromAmerican journal of cancer research · 2026
    Article
  7. 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

6 authors.

Mo ShaDepartment of Hepatobiliary and Pancreatic Surgery, The Second Hospital of Jilin University, Jilin University, Changchun, 130000, P. R. China.
Yang GaoDepartment of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, 150081, P. R. China.
Xu YinDepartment of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, 150081, P. R. China.
Xueyao LiDepartment of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, 150081, P. R. China.
Caiqi LiuDepartment of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, 150081, P. R. China. liucaiqi@ems.hrbmu.edu.cn.
Shuang LiDepartment of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, 150081, P. R. China. drlishuang@hrbmu.edu.cn.

Funding

China Postdoctoral Science Foundation 2024MD753935Haiyan Foundation of Harbin Medical University Cancer Hospital JJZD2024-08Heilongjiang Postdoctoral Financial Assistance LBH-Z23219Heilongjiang Provincial Institution of Higher Learning Basic Research Funds Basic Research Project 2023-KYYWF-0201Natural Science Foundation of Heilongjiang Province PL2024H158the National Funded Postdoctoral Researchers Program GZC20230641the National Natural Science Foundation of China 82400753
6 · The paper itself

Abstract

Pancreatic cancer (PC) is among the deadliest types of cancer, with very low chances of survival. It is often asymptomatic in the early stage, making diagnosis difficult. Therefore, it is typically found at an advanced stage, resulting in patients missing the opportunity for radical surgery. The complex biological characteristics of PC, coupled with the difficulties in drug delivery and tumor resistance, limit the effectiveness of drug therapy. Due to their compatibility with biological systems and low likelihood of triggering an immune response, exosomes are seen as a promising method for drug delivery. They are capable of targeting and penetrating tissues inside the body and can be engineered through surface modification and drug loading. Engineered exosomes possess controllable and diverse drug-carrying capabilities, which can enhance drug internalization and cellular uptake. Owing to their special properties and the potential to overcome the drawbacks of standard therapies, engineered exosomes have appeared as a promising treatment option. This review aims to comprehensively summarize the current application status and progress of engineered exosomes used in PC therapy.

Indexed as

Antineoplastic AgentsDrug Delivery SystemsExosomesPancreatic NeoplasmsAnimalsHumansAntineoplastic AgentsCancer therapyDelivery systemEngineered exosomesPancreatic cancer

Identifiers

PMID41024179
PMCPMC12482672

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Registered trials

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.