Tumor Microenvironment - How do cytokines act as regulators in tumor development?
May 16 , 2024
What is Tumor Microenvironment (TME)?
The tumor microenvironment (TME) is a constantly changing framework intricately linked with cancer cells, largely influenced by their presence. Distinctive traits of the TME include irregular blood vessels, hypoxia, acidic pH levels outside cells, modifications in the extracellular matrix, and stromal components like cancer-associated fibroblasts, macrophages, and immune cells (Marie-France Penet, Samata Kakkad & Jesus Pacheco-Torres, et.al, 2021)
Cytokines and the Tumor Microenvironment
Cytokines play a crucial role in the tumor microenvironment (TME) by acting as signaling molecules that mediate interactions between cancer cells and the surrounding stromal components. One of the three major characteristics of the TME is the presence of chronic inflammation. Chronic inflammation promotes cancer cell proliferation, matrix degradation and remodeling, angiogenesis, and immune suppression, thereby facilitating tumor growth, invasion, and metastasis. Inflammatory cytokines such as IL-4, IL-6, and IL-10 can activate M2-type macrophages, participate in the formation of Th2 cells, and promote the occurrence and development of tumors.
For example:
Tumor necrosis factor (TNF) and IL-1β, among others, are capable of promoting the survival and proliferation of tumor cells.
TNF and IL-6, among others, can disrupt cytokine regulation and promote tumor inflammation.
Cytokines’ clinical significance
Clinical application
Indicators
Significance
Auxiliary Diagnosis of the Type of Infectious Disease
Elevated levels of IL-1β, IL-6, and IL-8 in non-tumor patients
Suggests a possible bacterial infection
IFN-γ > 100 pg/ml in non-tumor patients.
Suggests the possibility of a mycobacterial infection
IFN-γ ≤ 100 pg/ml in non-tumor patients, along with elevated levels of IL-1β, IL-6, etc.
Suggests the possibility of a viral infection
Evaluation of Early Stage Infection, Severity of Infection, Inflammation, Sepsis, and Efficacy of Anti-inflammatory and Immunomodulatory Therapy
Elevated levels of IL-1β, IL-6, IL-8, IL-10, and IL-17 in infection and sepsis patients, often accompanied by decreased IL-2 levels.
Indicates the severity of infection or sepsis, with IL-1β, IL-6, IL-8, IL-10, and IL-17 levels typically elevated in such conditions.
Elevated levels of IL-2, IFN-γ, TNF-α, IL-1β, IL-6, IL-8, IL-10, and IL-12P70 in critically ill patients.
Indicates that the condition is critical, with significant infection present. In such cases, levels of IL-2, IFN-γ, TNF-α, IL-1β, IL-6, IL-8, IL-10, and IL-12P70 are often elevated.
To assist in the diagnosis of other diseases
IL-10 levels > 10% and elevated IFN-γ in patients
Suggests hemophagocytic syndrome; EBV infection needs to be ruled out. In pediatric EB viral infection patients, IFN-γ > 100 p/ml and IL-10 > 60 pg/ml, and IFN-γ>IL-6.
Elevated levels of IL-4, IL-5, and IL-17
Indicates the possibility of allergic diseases.
Applications in reproduction area
For patients with infertility or recurrent miscarriages, elevated levels of IL-2, IFN-γ, TNF-α, and IL-17, along with decreased levels of IL-10
Suggesting that the etiology of the patient's condition may be attributed to immune dysfunction, if during both passive and active treatments the levels of IL-2, IFN-γ, IFN-α, and IL-17 gradually decrease while the IL-10 level gradually increases, it indicates that the treatment is effective for the patient.
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Thirteen cytokines have been studied, and each factor can be matched as needed to solve various clinical treatment problems, such as distinguishing between viral and bacterial infections and real-time monitoring of treatment efficacy.
Marie-France Penet, Samata Kakkad, Jesus Pacheco-Torres, Santosh Bharti, Balaji Krishnamachary, Zaver M. Bhujwalla, Chapter 53 - Molecular and Functional Imaging and Theranostics of the Tumor Microenvironment, Editor(s): Brian D. Ross, Sanjiv Sam Gambhir, Molecular Imaging (Second Edition),Academic Press,2021,Pages 1007-1029, ISBN 9780128163863, https://doi.org/10.1016/B978-0-12-816386-3.00069-7.