Abstract

In recent years, several newly identified T helper (TH) cell subsets, such as TH9, TH17, and TH22 cells, and their respective cytokine products, IL-9, IL-17, and IL-22, have been reported to play critical roles in the development of chronic inflammation in the colorectum. Since chronic inflammation is a potent driving force for the development of human colorectal cancer (CRC), the contributions of TH9/IL-9, TH17/IL-17, and TH22/IL-22 in the pathogenesis of CRC have recently become an increasingly popular area of scientific investigation. Extensive laboratory and clinical evidence suggests a positive relationship between these new TH subsets and the growth and formation of CRC, whereas, administration of IL-9, IL-17, and IL-22 signaling inhibitors can significantly alter the formation of colorectal chronic inflammation or CRC lesions in animal models, suggesting that blocking these cytokine signals might represent promising immunotherapeutic strategies. This review summarizes recent findings and currently available data for understanding the vital role and therapeutic significance of TH9/IL-9, TH17/IL-17, and TH22/IL-22 in the development of colorectal tumorigenesis.

Highlights

  • Colorectal cancer (CRC) is one of the leading causes of high cancer-associated mortality worldwide

  • As the above findings indicated that TH9 and its cytokine product IL-9 are associated with the development of chronic inflammation in the colorectum, additional studies further analyzed the therapeutic effect of blocking IL-9 signaling in a colitis mouse model [66]

  • Current findings suggest a pivotal role of the TH subsets, TH17 and TH22, in the pathogenesis of CRC

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Summary

Introduction

Colorectal cancer (CRC) is one of the leading causes of high cancer-associated mortality worldwide. We have more recently demonstrated that a population of IL-9-positive cells and protein expression levels of IL-9 are greatly increased in mouse colitis-associated cancer (CAC) tissues, compared to those of control mouse tissues [82].

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