IP Library › Granted Patent US 10,921,311
Granted Patent B2
US 10,921,311 · App. 16/070,110 · Granted Feb 16, 2021

Fusions and method for detecting same

Inventors: Kengo Takeuchi (Tokyo, JP); Seiji Sakata (Tokyo, JP); Yuki Togashi (Tokyo, JP); Naoya Fujita (Tokyo, JP); Ryohei Katayama (Tokyo, JP)
Assignee: JAPANESE FOUNDATION FOR CANCER RESEARCH
G01N33/5011A61K31/519A61K38/005A61P35/00C07K14/82C12N9/12C12N9/88C12N15/113C12N15/62C12Y207/11025C12Y402/01047G01N33/57446C12Q1/686C12Q1/6853C12Q1/6886
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Quick Facts
Patent No.
US 10,921,311
App. No.
16/070,110
Granted
Feb 16, 2021
Kind
B2
Abstract

It is intended to reveal a polynucleotide serving as a novel causative gene of a cancer and, on the basis of this finding, to provide a method for detecting the polynucleotide or a polypeptide encoded thereby, a kit and a primer set for the detection, a method for screening for a substance that inhibits the polypeptide, and a pharmaceutical composition for the treatment of a cancer, containing the inhibiting substance. The detection method of the present invention detects a BRAF fusion protein or a fusion gene encoding the fusion protein, or a PXN or GMDS fusion protein or a fusion gene encoding the fusion protein in a digestive organ-derived sample obtained from a subject.

Claims (4)

1. A kit for detecting a PXN-BRAF fusion gene in a sample obtained from a subject, the kit comprising sense and antisense primers designed to be capable of specifically amplifying a polynucleotide encoding a polypeptide which is a fusion protein of the PXN protein with the BRAF protein,

wherein the sense primer consists of an oligonucleotide of at least 16 consecutive nucleotides arbitrarily selected from nucleotide positions 1 to 962 of SEQ ID NO: 1, and the antisense primer consists of an oligonucleotide complementary to an oligonucleotide of at least 16 consecutive nucleotides arbitrarily selected from nucleotide positions 963 to 2067 of SEQ ID NO: 1.

2. A method for detecting a PXN fusion gene encoding a fusion protein in a sample obtained from a subject, the method comprising detecting the PXN-BRAF fusion gene using the kit according to claim 1 , wherein the sample is DNA or mRNA.

3. The method according to claim 2 , wherein the sample is a digestive organ-derived sample.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 13, 2018
From: TAKEUCHI, KENGO; SAKATA, SEIJI; TOGASHI, YUKI; FUJITA, NAOYA; KATAYAMA, RYOHEI
To: JAPANESE FOUNDATION FOR CANCER RESEARCH
Reel/Frame 046348/0533 →
Priority Claims (1)
JP 2016-006471 · Jan 15, 2016 · national
Continuity (1)
Related Publication 20190033293A1 · Jan 31, 2019
Cited By (2)
US 12,203,127 US 12,559,799