IAPs in cancers: molecular mechanisms, clinical prognostic value, and translational therapeutic potential

Abstract Background Conventional therapies remain the primary approach for most cancers but typically achieve only modest improvements in prognosis. With the rapid advances in molecular biology and multi-omics technologies, targeted therapy has become the first choice for treating advanced cancer. Among these, inhibitor of apoptosis proteins (IAPs) has emerged as critical regulators in both experimental and clinical studies. Main body Nevertheless, several challenges persist, including tumor heterogeneity across cancer types, adverse effects associated with IAPs inhibitors (such as cytokine release and inflammation), and the lack of validated biomarkers for patient selection. With the development of artificial intelligence and precision medicine, IAP-targeted therapy, especially in combination with other therapies, has shown favorable clinical application potential. Conclusions: This review systematically summarizes the structural domains, molecular functions, biological processes, clinical relevance, and advances in drug development and translational applications of IAPs, aiming to refine therapeutic strategies and facilitate clinical translation.

Authors

Institutions

Publication Details

Journal
Journal of Translational Medicine
Published
2026-01-08
DOI
https://doi.org/10.1186/s12967-025-07640-7
Primary Topic
Protease and Inhibitor Mechanisms
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

IAPs in cancers: molecular mechanisms, clinical prognostic value, and translational therapeutic potential

Jing Xie, Zhisheng Teng, Liyun Teng
Journal of Translational Medicine
Protease and Inhibitor Mechanisms
article

IAPs in cancers: molecular mechanisms, clinical prognostic value, and translational therapeutic potential

Jing Xie, Zhisheng Teng, Liyun Teng
article en

Abstract

Abstract Background Conventional therapies remain the primary approach for most cancers but typically achieve only modest improvements in prognosis. With the rapid advances in molecular biology and multi-omics technologies, targeted therapy has become the first choice for treating advanced cancer. Among these, inhibitor of apoptosis proteins (IAPs) has emerged as critical regulators in both experimental and clinical studies. Main body Nevertheless, several challenges persist, including tumor heterogeneity across cancer types, adverse effects associated with IAPs inhibitors (such as cytokine release and inflammation), and the lack of validated biomarkers for patient selection. With the development of artificial intelligence and precision medicine, IAP-targeted therapy, especially in combination with other therapies, has shown favorable clinical application potential. Conclusions: This review systematically summarizes the structural domains, molecular functions, biological processes, clinical relevance, and advances in drug development and translational applications of IAPs, aiming to refine therapeutic strategies and facilitate clinical translation.

Journal of Translational MedicineVol. 24(1)
Wenzhou Medical University (CN), First Affiliated Hospital of Wenzhou Medical University (CN), Wenzhou Hospital of Traditional Chinese Medicine (CN), Zhejiang Cancer Hospital (CN), Hangzhou Cancer Hospital (CN)
Openalex Percentile: Top 94%
Protease and Inhibitor Mechanisms
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

IAPs in cancers: molecular mechanisms, clinical prognostic value, and translational therapeutic potential — Jing Xie, Zhisheng Teng, et al. · Journal of Translational Medicine (2026) | TGRS Research Map | TGRS