IP Library › Granted Patent US 12,404,540
Granted Patent B2
US 12,404,540 · App. 17/286,379 · Granted Sep 2, 2025

Epigenetic biomarker and uses therefor

Inventors: Abu Sina (St Lucia, AU); Matt Trau (St Lucia, AU); Laura Garcia Carrascosa (St Lucia, AU)
Assignee: THE UNIVERSITY OF QUEENSLAND
C12Q1/6809C12Q1/6886C12Q2600/154
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Quick Facts
Patent No.
US 12,404,540
App. No.
17/286,379
Granted
Sep 2, 2025
Kind
B2
Abstract

Disclosed is an epigenetic biomarker that comprises clustered methylated genomic DNA which can self-assemble to form complexes that have distinct physicochemical properties relative to genomic DNA that lacks such clusters. Also disclosed are methods, systems, compositions and kits that takes advantage of these physicochemical properties for detecting clustered methylated genomic DNA including for determining likelihood of the presence of cancer.

Claims (12)

1. A method for detecting and measuring cancer DNA, the method comprising:

exposing endogenous cancer DNA from a biological sample to a working electrode that comprises an electro-conductive material;

applying a potential to the working electrode; and

detecting an electrical signal from the working electrode that is indicative of adsorption of the endogenous cancer DNA to the electro-conductive material, wherein the electrical signal from the working electrode is different than another electrical signal generated from the working electrode when exposed to (1) one corresponding non-cancer DNA or (2) a total amount of endogenous cancer DNA from another biological sample that is different than a total amount of the endogenous cancer DNA from the biological sample.

2. The method of claim 1 , wherein the electro-conductive material is selected from the group consisting of gold, platinum, palladium, silver, carbon, alloys thereof, and composites thereof.

3. The method of claim 1 , wherein the electrical signal is selected from the group consisting of differential pulse voltammetry (DPV), cyclic voltammetry (CV), Linear Sweep Voltammetry (LSV), Square Wave Voltammetry (SWV), chronoamperometry, Electrochemical Impedance Spectroscopy (EIS), current, voltage, impedance, capacitance, charge, conductivity, resistance, and a combination thereof.

4. The method of claim 1 , wherein the biological sample comprises a biological fluid.

5. The method of claim 4 , wherein the biological fluid is selected from the group consisting of whole blood; lysed whole blood; serum; plasma; urine; sputum; sweat; follicular fluid; synovial fluid; amniotic fluid; a nasopharyngeal aspirate; a bronchial aspirate; semen; and cerebrospinal fluid.

6. The method of claim 1 , wherein the endogenous cancer DNA is selected from the group consisting of cellular genomic DNA (cellular gDNA), cell-free DNA (cfDNA), circulating tumor DNA (ctDNA), and extracellular vesicular DNA (evDNA).

7. The method of claim 1 , wherein the endogenous cancer DNA is derived from a subject that has been exposed to a treatment to treat a cancer.

8. The method of claim 7 , further comprising comparing the electrical signal to a threshold.

9. The method of claim 8 , wherein the threshold comprises a reference electrical signal that is indicative of a level of the cancer within the subject before the subject is exposed to the treatment.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 14, 2026
From: SINA, ABU ALI IBN; TRAU, MATHIAS; GARCIA CARRASCOSA, LAURA
To: THE UNIVERSITY OF QUEENSLAND
Reel/Frame 074663/0733 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 20, 2021
From: SINA, ABU; TRAU, MATT; GARCIA CARRASCOSA, LAURA
To: THE UNIVERSITY OF QUEENSLAND
Reel/Frame 055977/0110 →
Priority Claims (1)
AU 2018903935 · Oct 17, 2018 · national
Continuity (1)
Related Publication 20220033880A1 · Feb 3, 2022
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