Related Experiment Video
Updated: Jan 3, 2026

HPLC-based Assay to Monitor Extracellular Nucleotide/Nucleoside Metabolism in Human Chronic Lymphocytic Leukemia Cells
Published on: July 20, 2016
Inhibition of the Adenosinergic Pathway in Cancer Rejuvenates Innate and Adaptive Immunity
Juliana Hofstätter Azambuja1,2,3, Nils Ludwig2,3, Elizandra Braganhol1
1The Postgraduate Biosciences Program, Federal University of Health Sciences of Porto Alegre (UFCSPA), Porto Alegre 90050-170, RS Brazil.
Abstract:
The adenosine pathway plays a key role in modulating immune responses in physiological and pathological conditions. Physiologically, anti-inflammatory effects of adenosine balance pro-inflammatory adenosine 5'-triphosphate (ATP), protecting tissues from damage caused by activated immune cells. Pathologically, increased adenosine monophosphatase (AMPase) activity in tumors leads to increased adenosine production, generating a deeply immunosuppressed microenvironment and promoting cancer progression. Adenosine emerges as a promising target for cancer therapy. It mediates protumor activities by inducing tumor cell proliferation, angiogenesis, chemoresistance, and migration/invasion by tumor cells. It also inhibits the functions of immune cells, promoting the formation of a tumor-permissive immune microenvironment and favoriting tumor escape from the host immune system. Pharmacologic inhibitors, siRNA or antibodies specific for the components of the adenosine pathway, or antagonists of adenosine receptors have shown efficacy in pre-clinical studies in various in vitro and in vivo tumor models and are entering the clinical arena. Inhibition of the adenosine pathway alone or in combination with classic immunotherapies offers a potentially effective therapeutic strategy in cancer.
Insights
The adenosine pathway impacts immune responses, promoting cancer progression by creating an immunosuppressed tumor microenvironment. Inhibiting this pathway offers a promising cancer therapy strategy.
Area of Science:
- Immunology
- Cancer Biology
- Pharmacology
Background:
- The adenosine pathway modulates immune responses, balancing anti-inflammatory and pro-inflammatory signals.
- In cancer, elevated adenosine production creates an immunosuppressed microenvironment, promoting tumor growth and progression.
Purpose of the Study:
- To explore the role of the adenosine pathway in cancer immunology.
- To evaluate the therapeutic potential of targeting the adenosine pathway in cancer treatment.
Main Methods:
- Review of physiological and pathological roles of adenosine.
- Analysis of pre-clinical data on adenosine pathway inhibitors in various cancer models.
Main Results:
- Adenosine promotes tumor cell proliferation, angiogenesis, chemoresistance, and metastasis.
- Adenosine suppresses immune cell function, facilitating tumor immune escape.
- Pharmacological inhibition of the adenosine pathway shows efficacy in pre-clinical cancer models.
Conclusions:
- The adenosine pathway is a critical regulator of the tumor immune microenvironment.
- Targeting the adenosine pathway, alone or with immunotherapy, presents a viable therapeutic strategy for cancer.
Related Concept Videos
Adaptive Mechanisms in Cancer Cells
Some of the advantages that cancer cells have on normal cells include - enhanced ability to divide without terminally differentiating, induce new blood vessel formation,...
Tumor Immunotherapy
The Intrinsic Apoptotic Pathway
Cytotoxic T Cells-mediated Immune Response
Immunological surveillance is the ability of immune cells to monitor and eliminate infected cells with intracellular pathogens, neoplastically transformed cells, and cells with non-self antigens. Cytotoxic T cells and NK...
Inhibition of Cdk Activity
Cancer Therapies
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...

