Oncolytic Probiotics with Molecular Pili for Solid Tumor Therapy

Cell therapy and oncolytic viruses have emerged as promising cancer treatments but face significant challenges in solid tumors due to immune suppression and gene-related toxicities. Here, we selected a probiotic Lactobacillus rhamnosus (LR) that appears to exert oncolytic activity by inducing massive calcium influx, which subsequently triggers a lethal ROS burst in tumor cells. To reduce systemic toxicity and enhance oncolytic efficacy at the tumor site, we designed molecular pili (MP) targeting collagen-rich solid tumors and modified them into LRs via chemical coupling (LR@MP). In mouse models of colorectal cancer and melanoma, LR@MP increased intratumoral accumulation by two times and enhanced bacterial clearance from peripheral tissues. At a safe dose of 4 × 10<sup>5</sup> CFU, LR@MP inhibited 60%-80% of tumor growth. This dual-optimization strategy provides a new approach for next-generation in vivo therapies and warrants further preclinical evaluation.

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Publication Details

Journal
Advanced Science
Published
2026-02-03
DOI
https://doi.org/10.1002/advs.202517989
Primary Topic
Cancer Research and Treatments
Type
article
Field-Weighted Citation Impact
0.00

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article

Oncolytic Probiotics with Molecular Pili for Solid Tumor Therapy

S. L. Hu, Haodong Ge, Xia Yang, Hao Wang et al.
Advanced Science
Cancer Research and Treatments
article

Oncolytic Probiotics with Molecular Pili for Solid Tumor Therapy

S. L. Hu, Haodong Ge, Xia Yang, Hao Wang, Hao Zhong, Junjun Ma, Zhengwei Cai, Linke Bian, Changjie Yang, Yifan Qu, Minhua Zheng, Chengsheng Ding, Si Gao
article en

Abstract

Cell therapy and oncolytic viruses have emerged as promising cancer treatments but face significant challenges in solid tumors due to immune suppression and gene-related toxicities. Here, we selected a probiotic Lactobacillus rhamnosus (LR) that appears to exert oncolytic activity by inducing massive calcium influx, which subsequently triggers a lethal ROS burst in tumor cells. To reduce systemic toxicity and enhance oncolytic efficacy at the tumor site, we designed molecular pili (MP) targeting collagen-rich solid tumors and modified them into LRs via chemical coupling (LR@MP). In mouse models of colorectal cancer and melanoma, LR@MP increased intratumoral accumulation by two times and enhanced bacterial clearance from peripheral tissues. At a safe dose of 4 × 10<sup>5</sup> CFU, LR@MP inhibited 60%-80% of tumor growth. This dual-optimization strategy provides a new approach for next-generation in vivo therapies and warrants further preclinical evaluation.

Advanced Science
University of Science and Technology of China (CN), Shanghai Jiao Tong University (CN), Renji Hospital (CN), Ruijin Hospital (CN), Shanghai Cancer Institute (CN), State Key Laboratory of Oncogene and Related Genes (CN), Shanghai Institute of Hematology (CN)
National Natural Science Foundation of China, National Science and Technology Major Project, Ruijin Hospital
Good health and well-being
Openalex Percentile: Top 71%
Cancer Research and Treatments
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