Abstract

The microbiota is a complex ecosystem of active microorganisms resident in the body of mammals. Although the majority of these microorganisms resides in the distal gastrointestinal tract, high-throughput DNA sequencing technology has made possible to understand that several other tissues of the human body host their own microbiota, even those once considered sterile, such as lung tissue. These bacterial communities have important functions in maintaining a healthy body state, preserving symbiosis with the host immune system, which generates protective responses against pathogens and regulatory pathways that sustain the tolerance to commensal microbes. Toll-like receptors (TLRs) are critical in sensing the microbiota, maintaining the tolerance or triggering an immune response through the direct recognition of ligands derived from commensal microbiota or pathogenic microbes. Lately, it has been highlighted that the resident microbiota influences the initiation and development of cancer and its response to therapies and that specific changes in the number and distribution of taxa correlate with the existence of cancers in various tissues. However, the knowledge of functional activity and the meaning of microbiome changes remain limited. This review summarizes the current findings on the function of TLRs as sensors of the microbiota and highlighted their modulation as a reflection of tumor-associated changes in commensal microbiota. The data available to date suggest that commensal “onco-microbes” might be able to break the tolerance of TLRs and become complicit in cancer by sustaining its growth.

Highlights

  • All mammals harbor widely diverse active microbial communities, collectively termed the microbiota (Sender et al, 2016)

  • Toll-like receptors (TLRs) are able to discriminate between benign colonization and the presence of pathogens and have developed ways to be either responsive or protective against microbes

  • We demonstrated that TLR3 expression on tumor cells predicts a favorable outcome in Stage I NSCLC, whereas TLR3 expression on the immune cells infiltrating the tumor stroma was associated with a poor overall survival

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Summary

Introduction

All mammals harbor widely diverse active microbial communities, collectively termed the microbiota (Sender et al, 2016). These studies indicate that the discrimination between commensals and pathogens is guaranteed by several different strategies, most of which involve the modulation of expression and activation of TLRs. These mechanisms are crucial in sustaining the immune “tolerance” to the commensal microbiota and to maintain homeostasis.

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