Machine Learning‐Based Screening of Optimal miRNA Targets Enabled by a Cytosolic Delivery Carrier for Augmenting Cancer Therapy

H Hang Xu P Pengxiang Min (Key Laboratory of Modern Toxicology of Ministry of Education Nanjing Medical University Nanjing P. R. China) Y Yanbin Fu G Ge Sun (Pritzker School of Molecular Engineering) H Hui Wu M Mengqiao Pan (Shanghai Key Laboratory for Cancer Systems Regulation and Clinical Translation (CSRCT‐SHANGHAI) Renji Hospital Affiliated to Shanghai Jiao Tong University School of Medicine Shanghai P. R. China) C Chaoxian Zhao (State Key Laboratory of Systems Medicine for Cancer Shanghai Cancer Institute Renji Hospital Affiliated to Shanghai Jiao Tong University School of Medicine Shanghai P. R. China) J Jiatong Li Y Ying Wu Y Ying Xu B Bin Gu J Jiahua Pan L Lin Zhang P Peifeng Liu (State Key Laboratory of Systems Medicine for Cancer Shanghai Cancer Institute Renji Hospital Affiliated to Shanghai Jiao Tong University School of Medicine Shanghai P. R. China)

Abstract

ABSTRACT Nucleic acid therapeutics offer promise for precision cancer treatment, but are limited by inaccurate target selection and inefficient delivery. This work presents a therapeutic platform combining dual machine learning models (LASSO and RSF)‐based miRNA target screening with a modular biomimetic nanocarrier system. Systematic screening and experimental validation identify miR‐873 as a previously uncharacterized tumor‐suppressive miRNA in prostate cancer, and miR‐20a as oncogenic. Mechanistic studies reveal that they regulate HNRNPK and ABL2, modulating pathways involved in proliferation and metastasis. Then, the biomimetic nanocarrier, engineered with prostate cancer cell‐derived endoplasmic reticulum membrane (ERM), is successfully developed for cytosolic co‐delivery of miR‐873 mimic and miR‐20a inhibitor in prostate cancer, achieving significant and synergistic suppression of tumor proliferation and metastasis both in vitro and in vivo. Besides, co‐loading with docetaxel further enhances antitumor effects, underscoring its potential for combination therapies to inhibit cancer progression. These findings highlight both the therapeutic synergy of rationally selected miRNA combinations and the platform's versatility for precision cancer treatment.

Article Details

Volume / Issue Vol. 1, Issue 1
Published August 19, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (14)

H

Hang Xu

P

Pengxiang Min

Key Laboratory of Modern Toxicology of Ministry of Education Nanjing Medical University Nanjing P. R. China

Y

Yanbin Fu

G

Ge Sun

Pritzker School of Molecular Engineering

H

Hui Wu

M

Mengqiao Pan

Shanghai Key Laboratory for Cancer Systems Regulation and Clinical Translation (CSRCT‐SHANGHAI) Renji Hospital Affiliated to Shanghai Jiao Tong University School of Medicine Shanghai P. R. China

C

Chaoxian Zhao

State Key Laboratory of Systems Medicine for Cancer Shanghai Cancer Institute Renji Hospital Affiliated to Shanghai Jiao Tong University School of Medicine Shanghai P. R. China

J

Jiatong Li

Y

Ying Wu

Y

Ying Xu

B

Bin Gu

J

Jiahua Pan

L

Lin Zhang

P

Peifeng Liu

State Key Laboratory of Systems Medicine for Cancer Shanghai Cancer Institute Renji Hospital Affiliated to Shanghai Jiao Tong University School of Medicine Shanghai P. R. China