IP Library Granted Patent US 8,580,513
Granted Patent B2
US 8,580,513 · App. 13/172,047 · Granted Nov 12, 2013

Methods for determining response to neoadjuvant therapy and survival using MicroRNA-10b

Inventors: Lorenzo F. Sempere (Lebanon, NH); Murray Korc (Hanover, NH); Meir Preis (Hanover, NH)
Assignee: Trustees of Dartmouth College
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Quick Facts
Patent No.
US 8,580,513
App. No.
13/172,047
Granted
Nov 12, 2013
Kind
B2
Abstract

The present invention provides methods for determining response to neoadjuvant therapy and metastasis-free survival in pancreatic ductal adenocarcinoma based upon the level of microRNA expression and optionally the presence of a protein cancer cell marker in biological samples such as formalin-fixed paraffin-embedded specimens using in situ hybridization and optionally an immunohistochemical assay.

Claims (22)

1. A method for determining response to neoadjuvant therapy in pancreatic ductal adenocarcinoma (PDAC) comprising

(a) obtaining a biological sample from a patient with PDAC;

(b) determining the level of microRNA-10b in the biological sample with a microRNA-10b specific probe having the sequence 5′-CA+CAA+ATT+CGG+TT+CTA+CAG+GGTA-3′ (SEQ ID NO:3), wherein +N denotes a locked nucleic acid modified nucleotide;

(c) comparing the level of microRNA-10b in the biological sample to control samples expressing relatively low, medium or high levels of microRNA-10b; and

(d) diagnosing response of the patient to neoadjuvant therapy, wherein a level of microRNA-10b expression in the biological sample comparable to the control sample expressing a relatively low level of microRNA-10b indicates that the patient is likely to respond to neoadjuvant therapy.

2. A method for determining response to neoadjuvant therapy in pancreatic ductal adenocarcinoma (PDAC) comprising

(a) obtaining a biological sample from a patient with PDAC;

(b) detecting cytokeratin or mucin cancer cell marker-positive cells of the biological sample;

(c) determining the level of microRNA-10b in the cytokeratin or mucin cancer cell marker-positive cells;

(d) comparing the level of microRNA-10b in the cytokeratin or mucin cancer cell marker-positive cells to control cells expressing relatively low, medium or high levels of microRNA-10b; and

(e) diagnosing response of the patient to neoadjuvant therapy, wherein a level of microRNA-10b expression in the cytokeratin or mucin cancer cell marker-positive cells comparable to the control sample expressing a relatively low level of microRNA-10b indicates that the patient is likely to respond to neoadjuvant therapy.

3. A method for determining metastasis-free survival in pancreatic ductal adenocarcinoma (PDAC) comprising

(a) obtaining a biological sample from a patient with PDAC;

(b) determining the level of microRNA-10b in the biological sample with a microRNA-10b specific probe having the sequence 5′-CA+CAA+ATT+CGG+TT+CTA+CAG+GGTA-3′ (SEQ ID NO:3), wherein +N denotes a locked nucleic acid modified nucleotide;

(c) comparing the level of microRNA-10b in the biological sample to control samples expressing relatively low, medium or high levels of microRNA-10b; and

(d) diagnosing metastasis-free survival of the patient, wherein a level of microRNA-10b expression in the biological sample comparable to the control sample expressing a relatively low level of microRNA-10b indicates that the patient has an increase in metastasis-free survival.

4. A method for determining metastasis-free survival in pancreatic ductal adenocarcinoma (PDAC) comprising

(a) obtaining a biological sample from a patient with PDAC;

(b) detecting cytokeratin or mucin cancer cell marker-positive cells of the biological sample;

(c) determining the level of microRNA-10b in the cytokeratin or mucin cancer cell marker-positive cells;

(d) comparing the level of microRNA-10b in the cytokeratin or mucin cancer cell marker-positive cells to control cells expressing relatively low, medium or high levels of microRNA-10b; and

(e) diagnosing metastasis-free survival of the patient, wherein a level of microRNA-10b expression in the biological sample comparable to the control sample expressing a relatively low level of microRNA-10b indicates that the patient has an increase in metastasis-free survival.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jul 16, 2018
From: DARMOUTH COLLEGE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 046547/0510 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 18, 2011
From: SEMPERE, LORENZO F.; KORC, MURRAY; PREIS, MEIR
To: TRUSTEES OF DARTMOUTH COLLEGE
Reel/Frame 026606/0986 →
Continuity (6)
Continuation In Part PCTUS2011040624 · Jun 16, 2011
Provisional Application 61447882 · Mar 1, 2011
Provisional Application 61441694 · Feb 11, 2011
Provisional Application 61377245 · Aug 26, 2010
Provisional Application 61365945 · Jul 20, 2010
Related Publication 20120021415A1 · Jan 26, 2012