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Summary for Patent: 9,752,197
|Title:||Method for detecting methylation of colorectal cancer specific methylation marker gene for colorectal cancer diagnosis|
|Abstract:||The present invention relates to a method for detecting methylation of the bowel-cancer-specific methylation marker GPM6A (NM_201591, glycoprotein M6A) gene in order to diagnose bowel cancer, and more specifically relates to a method for providing information for diagnosing bowel cancer by detecting the methylation of a bowel-cancer-specific marker gene that is specifically methylated in bowel cancer cells. The method for detecting methylation and a diagnostic composition, kit and nucleic-acid chip according to the present invention can be used to advantage in diagnosing bowel cancer more accurately and quickly than by normal methods as they permit bowel cancer to be diagnosed at the initial genetic transformation step and so allow early diagnosis.|
|Inventor(s):||An; Sung Whan (Daejeon, KR), Oh; Tae Jeong (Daejeon, KR)|
|Assignee:||GENOMICTREE, INC. (Daejeon, KR)|
|Patent Claims:||1. A method for detecting CpG methylation of GPM6A (glycoprotein M6A) gene, the method comprising the steps of: (a) isolating genomic DNA from a clinical sample; (b)
treating the genomic DNA or a fragment thereof with bisulfite; (c) amplifying a methylated CpG of GPM6A gene in the bisulfite-treated genomic DNA or fragment thereof from step (b) by using primer(s) comprising sequence(s) selected from the group
consisting of SEQ ID Nos: 24 to 69; and (d) determining whether the CpG GPM6A was methylated based on whether the DNA was amplified in step (c).
2. The method of claim 1, wherein the step (c) is performed by detecting methylated CpG of the promoter or the CpG of the first intron of GPM6A gene.
3. The method of claim 2, wherein the first intron of GPM6A gene has a sequence of SEQ ID NO: 1.
4. The method of claim 1, wherein the detection of methylation is performed by a method selected from the group consisting of PCR, methylation-specific PCR, real-time methylation-specific PCR, quantitative PCR, pyrosequencing, and bisulfite sequencing.
5. The method of claim 1, wherein the clinical sample is selected from the group consisting of a tissue, cell, blood, blood plasma, serum, feces, and urine from a patient suspected of cancer or a subject to be diagnosed.
6. The method of claim 1, further comprising using probe(s) capable of hybridizing with a methylated CpG of GPM6A comprising at least one or more CpG dinucleotide in a region which hybridizes to the methylated CpG of GPM6A.
7. The method of claim 6, wherein the probe(s) comprises sequence(s) selected from the group consisting of SEQ ID NOS: 70-92.
Summary for Patent: Start Trial
|Foriegn Application Priority Data|
|Foreign Country||Foreign Patent Number||Foreign Patent Date|
|South Korea||10-2010-0129208||Dec 16, 2010|
|Applicant||Tradename||Biologic Ingredient||Dosage Form||BLA||Number||Approval Date||Patent No.||Assignee||Estimated Patent Expiration||Status||Orphan||Source|
|Schering||INTRON A||interferon alfa-2b||VIAL||103132||001||1986-06-04||Start Trial||GENOMICTREE, INC. (Daejeon, KR)||2030-12-16||RX||search|
|Schering||INTRON A||interferon alfa-2b||VIAL||103132||002||1986-06-04||Start Trial||GENOMICTREE, INC. (Daejeon, KR)||2030-12-16||RX||search|
|Schering||INTRON A||interferon alfa-2b||VIAL||103132||003||1986-06-04||Start Trial||GENOMICTREE, INC. (Daejeon, KR)||2030-12-16||RX||search|
|>Applicant||>Tradename||>Biologic Ingredient||>Dosage Form||>BLA||>Number||>Approval Date||>Patent No.||>Assignee||>Estimated Patent Expiration||>Status||>Orphan||>Source|
|Country||Patent Number||Publication Date|
|World Intellectual Property Organization (WIPO)||2012081928||Aug 23, 2012|
|World Intellectual Property Organization (WIPO)||2012081928||Jun 21, 2012|
|United States of America||2014045180||Feb 13, 2014|
|United States of America||2016145694||May 26, 2016|
|United States of America||2017335407||Nov 23, 2017|
|>Country||>Patent Number||>Publication Date|
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