Methods and systems of using exosomes for determining phenotypes
View Patent ↗Exosomes can be used for detecting biomarkers for diagnostic, therapy-related or prognostic methods to identify phenotypes, such as a condition or disease, for example, the stage or progression of a disease. Cell-of-origin exosomes can be used in profiling of physiological states or determining phenotypes. Biomarkers or markers from cell-of-origin specific exosomes can be used to determine treatment regimens for diseases, conditions, disease stages, and stages of a condition, and can also be used to determine treatment efficacy. Markers from cell-of-origin specific exosomes can also be used to identify conditions of diseases of unknown origin.
1. A method of characterizing prostate cancer in a subject comprising:
a) identifying a bio-signature of one or more exosome isolated from said subject, comprising:
(i) determining the presence or level of CD9, CD63, or CD81 protein, or a combination thereof, from said one or more isolated exosome;
(ii) determining the presence or level of PSMA and/or PCSA protein from said one or more isolated exosome;
(iii) determining the presence or level of B7H3 and/or EpCam protein from said one or more isolated exosome; and
b) comparing said presence or levels of said proteins from said isolated exosome to a reference, wherein elevated presence or levels as compared to said reference indicate that said subject may be predisposed to or afflicted with prostate cancer, thereby characterizing said prostate cancer.
2. A method of assessing prostate cancer in a subject comprising:
identifying a bio-signature of one or more exosome isolated from said subject, comprising:
determining the levels of CD9, CD63 and CD81 proteins from said one or more isolated exosome;
determining the levels of PSMA and PCSA proteins from said one or more isolated exosome;
determining the level of B7H3 protein from said one or more isolated exosome; and
comparing said levels of said proteins from said one or more isolated exosome to a reference,
wherein elevated levels as compared to said reference indicate that said subject may be predisposed to or afflicted with prostate cancer, thereby assessing said prostate cancer.
3. The method of claim 1 , wherein said one or more isolated exosome is obtained from a sample of bodily fluid from said subject.
4. The method of claim 3 , wherein the volume of said sample is less than 2 mL.
5. The method of claim 3 , wherein said bodily fluid is peripheral blood, serum, plasma, ascites, urine, cerebrospinal fluid (CSF), sputum, saliva, bone marrow, synovial fluid, aqueous humor, cerumen, broncheoalveolar lavage fluid, semen, prostatic fluid, cowper's fluid or pre-ejaculatory fluid, sweat, fecal matter, tears, cyst fluid, pleural and peritoneal fluid, lymph, chyme, chyle, bile, intestinal fluid, pus, sebum, vomit, mucosal secretion, stool water, pancreatic juice, lavage fluids from sinus cavities, or bronchopulmonary aspirates.
6. The method of claim 1 or 2 , wherein said one or more isolated exosome has a diameter of about 30 nm to about 800 nm.
7. The method of claim 1 or 2 , wherein said one or more isolated exosome has a diameter of about 30 nm to about 200 nm.
8. The method of claim 1 or 2 , wherein said one or more isolated exosome is isolated from said biological sample with size exclusion chromatography, density gradient centrifugation, differential centrifugation, nanomembrane ultrafiltration, immunoabsorbent capture, affinity purification, microfluidic separation or a combination thereof.
9. The method of claim 3 , wherein said sample comprises urine, plasma or serum.
10. The method of claim 1 or 2 , wherein said determining comprises measuring an expression level, presence, absence, mutation, truncation, insertion, modification, sequence variation or molecular association of said proteins from said one or more isolated exosome.
11. The method of claim 1 or 2 , wherein said characterizing comprises one or more of determining an amount of exosomes, a temporal evaluation of a variation in exosome half-life, a temporal evaluation of circulating exosome half-life, a temporal evaluation of exosome metabolic half-life, or determining a exosome activity.
12. The method of claim 1 , wherein identifying said bio-signature comprises determining the presence or level of at least proteins CD9, PCSA, CD63, CD81, PSMA and B7H3.
13. The method of claim 1 or 2 , wherein said bio-signature comprises one or more binding agent that is specific for at least one of said proteins from said one or more isolated exosome.
14. The method of claim 13 , wherein said one or more binding agent is an antigen, DNA molecule, RNA molecule, antibody, antibody fragment, aptamer, peptoid, zDNA, peptide nucleic acid (PNA), locked nucleic acids (LNA), lectin, peptide, dendrimer or chemical compound.
15. The method of claim 1 or 2 , wherein said characterizing comprises a diagnosis, prognosis, determination of drug efficacy, monitoring the status of said subject's response or resistance to a treatment or selection of a treatment for said prostate cancer.
16. The method of claim 15 , wherein said subject is non-responsive to a current therapeutic being administered to said subject.
17. The method of claim 16 , wherein said therapeutic is a cancer therapeutic.
18. The method of claim 1 or 2 , wherein said reference is derived from said bio-signature identified in said subject over a time course.
19. The method of claim 3 , wherein said sample is plasma.
20. The method of claim 19 , wherein said characterizing comprises a diagnosis, prognosis, determination of drug efficacy, monitoring the status of said subject's response or resistance to a treatment or selection of a treatment for said prostate cancer.
21. The method of claim 19 , wherein said subject is non-responsive to a current therapeutic being administered to said subject.
22. The method of claim 19 , wherein said therapeutic is a cancer therapeutic.
23. The method of claim 19 , wherein said bio-signature comprises one or more binding agent that is specific for at least one of said proteins from said one or more isolated exosome.
24. The method of claim 23 , wherein said one or more binding agent is an antigen, DNA molecule, RNA molecule, antibody, antibody fragment, aptamer, peptoid, zDNA, peptide nucleic acid (PNA), locked nucleic acids (LNA), lectin, peptide, dendrimer or chemical compound.
25. The method of claim 1 or 2 , wherein said identifying is performed in a single assay.