MLchartDataset catalogue

Adenosine receptor A2A/A2B antagonist M1069

Term · Oncology and biomedicine · MLC-T-ONC-009670

An orally bioavailable antagonist of both the immunomodulatory checkpoint molecules adenosine A2A receptor (A2AR; ADORA2A) and A2B receptor (A2BR; ADORA2B), with potential immunomodulating and antineoplastic activities. Upon oral administration, adenosine A2A/A2B receptor antagonist M1069 competes with tumor-released adenosine for binding to A2AR and A2BR expressed on numerous intratumoral immune cells, such as dendritic cells (DCs), natural killer (NK) cells, macrophages and T lymphocytes. The binding of M1069 to A2AR and A2BR inhibits A2AR/A2BR activity and prevents adenosine-A2AR/A2BR-mediated signaling. A2AR/A2BR inhibition activates and enhances the proliferation of various immune cells, abrogates the adenosine-mediated immunosuppression in the tumor microenvironment (TME) and activates the immune system to exert anti-tumor immune responses against cancer cells, which leads to tumor cell killing. A2AR and A2BR, G protein-coupled signaling receptors, are expressed on the cell surfaces of numerous immune cells. Adenosine is often overproduced by tumor cells and plays a key role in immunosuppression and tumor cell proliferation.

Table 1. Record
IdentifierMLC-T-ONC-009670
FieldOncology and biomedicine
SynonymsA2A/A2B adenosine receptor antagonist M1069; A2AR/A2BR antagonist M1069; dual adenosine receptor antagonist M1069
ReferencesNational Cancer Institute Thesaurus (CC BY 4.0)
Record as JSON
{
  "id": "MLC-T-ONC-009670",
  "term": "Adenosine receptor A2A/A2B antagonist M1069",
  "field": "Oncology and biomedicine",
  "definition": "An orally bioavailable antagonist of both the immunomodulatory checkpoint molecules adenosine A2A receptor (A2AR; ADORA2A) and A2B receptor (A2BR; ADORA2B), with potential immunomodulating and antineoplastic activities. Upon oral administration, adenosine A2A/A2B receptor antagonist M1069 competes with tumor-released adenosine for binding to A2AR and A2BR expressed on numerous intratumoral immune cells, such as dendritic cells (DCs), natural killer (NK) cells, macrophages and T lymphocytes. The binding of M1069 to A2AR and A2BR inhibits A2AR/A2BR activity and prevents adenosine-A2AR/A2BR-mediated signaling. A2AR/A2BR inhibition activates and enhances the proliferation of various immune cells, abrogates the adenosine-mediated immunosuppression in the tumor microenvironment (TME) and activates the immune system to exert anti-tumor immune responses against cancer cells, which leads to tumor cell killing. A2AR and A2BR, G protein-coupled signaling receptors, are expressed on the cell surfaces of numerous immune cells. Adenosine is often overproduced by tumor cells and plays a key role in immunosuppression and tumor cell proliferation.",
  "synonyms": [
    "A2A/A2B adenosine receptor antagonist M1069",
    "A2AR/A2BR antagonist M1069",
    "dual adenosine receptor antagonist M1069"
  ],
  "references": [
    "National Cancer Institute Thesaurus"
  ],
  "url": "https://mlchart.com/terminology/oncology/adenosine-receptor-a2a-a2b-antagonist-m1069/"
}

Record 403 of 17,717 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.