Inflammation and carcinogenesis: molecular targets and small-molecule intervention strategies

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Authors: Wan‐Jung Lu, Ritu Ojha, Mandeep Rana, Vinod Gautam, Jiun-Yi Li, Shao-An Wang
Cited by: 3
References: 410

Abstract

NF-kB, JAK-STAT, inflammasomes, reactive oxygen species (ROS), and cytokine network, if left unanswered, foster the tumour-supportive environment. Within the tumour microenvironment (TME), inflammatory cells, in combination with stromal and cancerous cells, modulate these pathways and regulate critical tumour hallmarks. Therefore, efforts have been made to understand and tackle the interface between the inflammation-cancer axis, but therapeutic outcomes remain limited. In this context, integrating systems-level biological insights with precision-driven medicinal chemistry may pave the way towards next-generation anti-inflammatory chemotherapeutics. The current review underlines the critical involvement of inflammation in cancer development by providing a comprehensive overview of key molecular pathways. A special emphasis was placed on understanding the medicinal chemistry campaign over the last 5 years for the development of inflammation-targeting small-molecule therapeutics in cancer.

Fields of Study & Subjects

NF-κB Signaling Pathways Cytokine Signaling Pathways and Interactions Inflammasome and immune disorders

Publication details

Journal / source
Journal of Enzyme Inhibition and Medicinal Chemistry
Publisher
Informa UK Limited
Volume
41
Issue
1
Pages
2689287–2689287
Publication date
26 June 2026
Language
EN