MLchartDataset catalogue

anti-c-Met antibody-drug conjugate YL211

Term · Oncology and biomedicine · MLC-T-ONC-010531

An antibody-drug conjugate (ADC) composed of a humanized monoclonal antibody directed against the tumor-associated antigen (TAA) proto-oncogene c-Met (hepatocyte growth factor receptor; HGFR) site-specifically conjugated, via a tumor microenvironment (TME) activable protease-cleavable linker, to a topoisomerase 1 inhibitor (TOP1i), with potential antineoplastic activity. Upon administration of anti-c-Met ADC YL211, the anti-c-Met antibody moiety targets and binds to c-Met expressed on tumor cells. Upon proteolytic cleavage in the TME and the release of the topoisomerase I inhibitor, the topoisomerase I inhibitor targets and binds to DNA topoisomerase I, thereby inhibiting DNA replication and killing the c-Met-expressing cancer cells. In addition, YL211 is able to induce a bystander effect on neighboring cells. This further inhibits tumor cell proliferation. c-Met, a receptor tyrosine kinase overexpressed or mutated in many tumor cell types, plays key roles in tumor cell proliferation, survival, invasion, metastasis and tumor angiogenesis.

Table 1. Record
IdentifierMLC-T-ONC-010531
FieldOncology and biomedicine
Synonymsanti-c-Met ADC YL211; anti-c-Met/TOP1i ADC YL211; anti-c-Met/TOP1i antibody-drug conjugate YL211
ReferencesNational Cancer Institute Thesaurus (CC BY 4.0)
Record as JSON
{
  "id": "MLC-T-ONC-010531",
  "term": "anti-c-Met antibody-drug conjugate YL211",
  "field": "Oncology and biomedicine",
  "definition": "An antibody-drug conjugate (ADC) composed of a humanized monoclonal antibody directed against the tumor-associated antigen (TAA) proto-oncogene c-Met (hepatocyte growth factor receptor; HGFR) site-specifically conjugated, via a tumor microenvironment (TME) activable protease-cleavable linker, to a topoisomerase 1 inhibitor (TOP1i), with potential antineoplastic activity. Upon administration of anti-c-Met ADC YL211, the anti-c-Met antibody moiety targets and binds to c-Met expressed on tumor cells. Upon proteolytic cleavage in the TME and the release of the topoisomerase I inhibitor, the topoisomerase I inhibitor targets and binds to DNA topoisomerase I, thereby inhibiting DNA replication and killing the c-Met-expressing cancer cells. In addition, YL211 is able to induce a bystander effect on neighboring cells. This further inhibits tumor cell proliferation. c-Met, a receptor tyrosine kinase overexpressed or mutated in many tumor cell types, plays key roles in tumor cell proliferation, survival, invasion, metastasis and tumor angiogenesis.",
  "synonyms": [
    "anti-c-Met ADC YL211",
    "anti-c-Met/TOP1i ADC YL211",
    "anti-c-Met/TOP1i antibody-drug conjugate YL211"
  ],
  "references": [
    "National Cancer Institute Thesaurus"
  ],
  "url": "https://mlchart.com/terminology/oncology/anti-c-met-antibody-drug-conjugate-yl211/"
}

Record 1,622 of 17,721 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.