Zhuosheng Liu

Mr. Zhuosheng Liu

orcid

Research Focus & Metrics

Academic Career Length

2Years (2025-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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28 October 2025 in Cancers
Verified
Journal Article
Open access
PDF file
PLPeizhong Liu
Peizhong Liu
YRYidan Ruan
Yidan Ruan
YFYuling Fan
Yuling Fan
PLPing Li
Ping Li
ZLZhuosheng Liu
Zhuosheng Liu
SLShunlan Liu
Shunlan Liu
Background: Ovarian cancer is the deadliest female reproductive malignancy. Accurate preoperative differentiation of benign and malignant ovarian masses is critical for appropriate treatment. O-RADS category 4 lesions present a wide range of malignant risk, challenging radiologists. Ultrasonic images are the primary focus of current deep learning models, with no consideration for clinical data. Methods: We proposed OTC-NET, a model that uses multimodal data for classification, which combines ultrasound images and clinical information to improve the classification ability of O-RADS 4 ovarian masses. Results: OTC-NET outperforms seven deep learning models and three radiologists of varying experience, with AUC significantly higher than junior (p < 0.001), intermediate (p < 0.01), and senior (p < 0.05) radiologists. Additionally, OTC-NET–assisted diagnosis notably improves AUC and accuracy of junior and senior radiologists (p < 0.05). Conclusions: These results indicate that OTC-NET provides superior diagnostic accuracy and has strong potential for clinical application.

Verified
Journal Article
Open access
PDF file
ZLZhuosheng Liu
Zhuosheng Liu
FWFucai Wang
Fucai Wang
ZZZhihan Zhou
Zhihan Zhou
MWMei Wu
Mei Wu
QHQinghua Huang
Qinghua Huang
LYLiuting Ye
Liuting Ye
This article reviews the research progress for high-mobility group protein B1 (HMGB1) and its signaling pathway in osteosarcoma (OS) and discusses its application potential in targeted therapy. A large number of domestic and foreign studies were reviewed to summarize the research results on the the biological function, signal pathway regulation mechanism, and intervention strategy of HMGB1 in recent years. HMGB1 promotes OS cell proliferation, invasion, and immune escape by activating RAGE, TLR4, and downstream MAPK, NF-κB, and PI3K/AKT signaling pathways. Interfering with HMGB1 or its signaling axis shows good antitumor potential in in vitro and in vivo models, but clinical transformation is still limited by its dual biological effects and tumor heterogeneity. HMGB1 and its related signaling pathways are important targets for the treatment of osteosarcoma. In the future, the development of a multi-channel combined intervention and efficient delivery system will provide a new direction for improving the therapeutic effect.