IP Library Granted Patent US 9,631,241
Granted Patent B2
US 9,631,241 · App. 15/002,725 · Granted Apr 25, 2017

Complex sets of miRNAs as non-invasive biomarkers for colon cancer

Inventors: Andreas Keller (Püttlingen, DE); Markus Beier (Weinheim, DE); Eckart Meese (Hütschenhausen, DE); Petra Leidinger (Wadern-Nunkirchen, DE); Anke Wendschlag (Mannheim, DE)
Assignee: Comprehensive Biomarker Center GmbH
C12Q1/6886C12Q2600/112C12Q2600/118C12Q2600/158C12Q2600/16C12Q2600/178
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Quick Facts
Patent No.
US 9,631,241
App. No.
15/002,725
Filed
Jan 21, 2016
Granted
Apr 25, 2017
Kind
B2
Art Unit
1674
USPC
435/6
Abstract

Described herein are non-invasive methods, kits and means for diagnosing and/or prognosing of colon cancer a body fluid sample from a subject. Further described herein are sets of polynucleotides or sets of primer pairs for detecting sets of miRNAs for diagnosing and/or prognosing of colon cancer in a body fluid sample from a subject. In addition, described herein are sets of miRNAs for diagnosing and/or prognosing of colon cancer in a body fluid sample from a subject.

Claims (30)

1. A method for detecting altered levels of miRNA expression in a human subject having, or suspected of having, colon cancer comprising the steps of:

(i) determining an expression profile of a set comprising at least two miRNAs representative for colon cancer in a blood cell sample from the human subject,

wherein the blood cell sample consists of a mixture of erythrocytes, leukocytes, and thrombocytes,

wherein the miRNAs comprised in the set comprising at least two miRNAs are selected from the group consisting of:

hsa-miR-20a, hsa-miR-144*, hsa-miR-183, hsa-miR-499-3p, hsa-miR-658, hsa-miR-208b, hsa-miR-145, hsa-miR-28-3p, hsa-miR-18a, hsa-miR-646, hsa-miR-17, hsa-miR-19b, hsa-miR-596, hsa-miR-664, hsa-miR-1180, hsa-miR-20b, hsa-miR-106a, hsa-miR-564, hsa-miR-93, hsa-miR-183*, hsa-miR-1260, hsa-miR-373, hsa-miR-1227, hsa-miR-483-5p, hsa-miR-621, hsa-miR-1908, hsa-miR-106b, hsa-miR-607, hsa-miR-374a, hsa-miR-224, hsa-miR-17*, hsa-miR-130b, hsa-miR-1246, hsa-miR-635, hsa-miR-146a, hsa-miR-144, hsa-miR-523, hsa-miR-454, hsa-miR-296-5p, hsa-miR-1226*, hsa-miR-496, hsa-miR-216a, hsa-miR-613, hsa-miR-200a*, hsa-miR-1225-5p, hsa-miR-328, hsa-miR-556-5p, hsa-miR-1247, hsa-miR-1294, hsa-miR-609, hsa-miR-1282, hsa-miR-485-5p, hsa-miR-520d-3p, hsa-miR-1251, hsa-miR-151-3p, hsa-miR-593*, hsa-miR-361-5p, hsa-miR-720, hsa-miR-452*, hsa-miR-216b, hsa-miR-32, hsa-miR-934, hsa-miR-640, hsa-miR-34a*, hsa-let-7d*, hsa-miR-197, hsa-miR-423-5p, hsa-miR-214*, hsa-miR-574-3p, hsa-miR-604, hsa-miR-1324, hsa-miR-320d, hsa-miR-151-5p, hsa-miR-744, hsa-miR-33b, hsa-miR-455-3p, hsa-miR-483-3p, hsa-miR-891b, hsa-miR-219-2-3p, hsa-miR-892a, hsa-miR-1272, hsa-miR-153, hsa-miR-31*, hsa-miR-654-5p, hsa-miR-125a-3p, and hsa-miR-545, and

wherein the set comprising at least two miRNAs comprises at least one of the sets of miRNAs listed in FIG. 2 , FIG. 5 b or FIG. 7 ; and

(ii) comparing said expression profile to a reference expression profile obtained from at least one healthy human subject, or a human subject not having , or being suspected of having colon cancer;

(iii) detecting at least one of the following up-regulations relative to the reference expression profile of:

hsa-miR-183, hsa-miR-658, hsa-miR-145, hsa-miR-28-3p, hsa-miR-19b, hsa-miR-664, hsa-miR-1180, hsa-miR-183*, hsa-miR-1260, hsa-miR-373, hsa-miR-1227, hsa-miR-483-5p, hsa-miR-1908, hsa-miR-224, hsa-miR-130b, hsa-miR-1246, hsa-miR-146a, hsa-miR-296-5p, hsa-miR-613, hsa-miR-1225-5p, hsa-miR-328, hsa-miR-1294, hsa-miR-609, hsa-miR-520d-3p, hsa-miR-151-3p, hsa-miR-361-5p, hsa-miR-720, hsa-let-7d*, hsa-miR-197, hsa-miR-423-5p, hsa-miR-574-3p, hsa-miR-320d, hsa-miR-151-5p, hsa-miR-483-3p, hsa-miR-219-2-3p, hsa-miR-892a, hsa-miR-125a-3p, hsa-miR-1282, or hsa-miR-744, and/or

at least one of the following down-regulations relative to the reference expression profile of:

hsa-miR-20a, hsa-miR-144*, hsa-miR-499-3p, hsa-miR-208b, hsa-miR-18a, hsa-miR-646, hsa-miR-17, hsa-miR-596, hsa-miR-20b, hsa-miR-106a, hsa-miR-564, hsa-miR-93, hsa-miR-621, hsa-miR-106b, hsa-miR-607, hsa-miR-374a, hsa-miR-17*, hsa-miR-635, hsa-miR-144, hsa-miR-523, hsa-miR-454, hsa-miR-1226*, hsa-miR-496, hsa-miR-216a, hsa-miR-200a*, hsa-miR-556-5p, hsa-miR-1247, hsa-miR-485-5p, hsa-miR-1251, hsa-miR-593*, hsa-miR-452*, hsa-miR-216b, hsa-miR-32, hsa-miR-934, hsa-miR-640, hsa-miR-34a*, hsa-miR-214*, hsa-miR-604, hsa-miR-1324, hsa-miR-33b, hsa-miR-455-3p, hsa-miR-891b, hsa-miR-1272, hsa-miR-153, hsa-miR-31*, hsa-miR-654-5p, or hsa-miR-545, and

(iv) determining whether the subject has colon cancer or will develop colon cancer by transforming the individual expression levels of the miRNAs in the individual blood cells of the blood cell sample to one numerical value which represents the mathematical average of the miRNA expression levels of the individual blood cells, wherein the individual blood cells are erythrocytes, leukocytes, and thrombocytes.

2. The method of claim 1 , wherein the expression profile of the miRNAs is determined comprising the steps:

(a) extracting total RNA from said blood sample,

(b) reverse-transcribing the total RNA into cDNA, and

(c) amplifying the cDNA and thereby detecting the miRNA levels in said blood sample.

3. A kit for diagnosing and/or prognosing colon cancer according to the method of claim 1 , comprising

(i) means for determining the expression profile of the set comprising at least two miRNAs representative for colon cancer in the blood sample from the subject, and

(ii) at least one reference,

wherein the reference is determined from reference expression profiles of at least 2 control subjects with at least 2 clinical conditions, from which at least one is colon cancer.

4. The kit according to claim 3 , wherein the reference is determined in the same type of blood sample as the subject to be diagnosed and/or prognosed.

5. The kit according to claim 4 , wherein the means comprise:

(i) a set of at least two polynucleotides or a set of at least two primer pairs for detecting the set comprising at least two miRNAs for diagnosing and/or prognosing colon cancer in the blood sample from a subject, wherein the nucleotide sequences of the miRNAs comprised in the set are selected from the group consisting of SEQ ID NOs: 1 to 588, and

(ii) a biochip, a RT-PCT system, a PCR-system, a flow cytometer, a bead-based multiplex system or a next generation sequencing system.

6. A method of detecting an expression profile for colon cancer in a subject comprising the steps of:

(i) providing a blood cell sample consisting of a mixture of erythrocytes, leukocytes, and thrombocytes obtained from the subject, and

(i.) detecting whether the expression profile for colon cancer is present in the blood cell sample obtained from the subject by contacting the blood cell sample with probes for a miRNA expression profile and detecting binding between the probes and the miRNAs,

wherein the expression profile comprises a set of at least two miRNAs representative for colon cancer in the blood cell sample,

wherein the set of at least two miRNAs comprises at least one of the sets of miRNAs listed in FIG. 2 , FIG. 5 b or FIG. 7 ; and,

determinin whether the subject has colon cancer or will develop colon cancer by transforming the individual expression levels of the miRNAs in the individual blood cells of the blood cell sample to one numerical value which represents the mathematical average of the miRNA expression levels of the individual blood cells, wherein the individual blood cells are erythrocytes, leukocytes, and thrombocytes.

Assignments (3)
CHANGE OF NAME Recorded Mar 14, 2017
From: COMPREHENSIVE BIOMARKER CENTER GMBH
To: HUMMINGBIRD DIAGNOSTICS GMBH
Reel/Frame 041994/0243 →
CHANGE OF NAME Recorded Mar 14, 2017
From: COMPREHENSIVE BIOMARKER CENTER GMBH
To: HUMMINGBIRD DIAGNOSTICS GMBH
Reel/Frame 041994/0249 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 21, 2016
From: KELLER, ANDREAS; BEIER, MARKUS; MEESE, ECKART; LEIDINGER, PETRA; WENDSCHLAG, ANKE
To: COMPREHENSIVE BIOMARKER CENTER GMBH
Reel/Frame 038340/0448 →
Priority Claims (1)
EP 11178155 · Aug 19, 2011 · regional
Continuity (2)
Division 14239264
Related Publication 20160138117A1 · May 19, 2016