Targeting treatment for ADAM30 in pathological cells
Described herein are methods and systems using ADAM30 as a biomarker to help early diagnosis of congenital malformed vasculatures in children and which can also serve as a companion diagnostic biomarker for malformed vasculatures, as well as a subpopulation of cancer cells, wherein blockage of activity of ADAM30 by a neutralized antibody or inhibitor can be used as a treatment strategy for those ADAM30-positive vascular endothelial cells and cancer cells.
1. Methods for detecting congenital vascular malformations comprising:
obtaining at least one body fluid sample from a subject;
introducing at least one human or humanized antibody having at least two binding specificities for at least two different antigens to the at least one body fluid sample wherein the at least one human or humanized antibody compound is configured to bind to at least one domain of at least one biomarker comprising an ADAM30 protein or polypeptide thereof present in the at least one body fluid sample;
wherein binding of the at least one human or humanized antibody to the at least one domain of the at least one biomarker forms an assay;
wherein the presence of the at least one biomarker in the body fluid, whether analyzed in vivo or in vitro, indicates a vascular disease or disorder associated with aberrant ADAM30 expression or activity in the subject; and
wherein formation of the assay determines when there is an increase in ADAM30 to administer a therapeutically effective amount of a therapeutic agent to treat the vascular disease or disorder.
2. The method of claim 1 , wherein the biomarker has a genetic sequence of SEQ. ID. NO.: 1.
3. The method of claim 1 , further comprising identifying Sturge-Weber syndrome via the presence of the at least one biomarker.
4. The method of claim 1 , further comprising differentiating cancer cell subtypes via the presence of the at least one biomarker.