Oligodendroglioma drive genes

Patent metadata

Field	Value
Publication number	US-9873917-B2
Application number	US-201214233296-A
Country	US
Kind code	B2
Filing date	Jul 18, 2012
Priority date	Jul 19, 2011
Publication date	Jan 23, 2018
Grant date	Jan 23, 2018

Abstract

Oligodendrogliomas are the second most common malignant brain tumor in adults. These tumors often contain a chromosomal abnormality involving a pericentromeric fusion of chromosomes 1 and 19, resulting in losses of the entire short arm of the former and the long arm of the latter. To identify the molecular genetic basis for this alteration, we performed exomic sequencing of seven anaplastic oligodendrogliomas with chromosome 1p and 19q losses. Among other changes, we found that that CIC (homolog of the Drosophila gene capicua) on chromosome 19q was somatically mutated in six of the seven cases and that FUBP1 (far upstream element (FUSE) binding protein) on chromosome 1p was somatically mutated in two of the seven cases. Examination of 27 additional oligodendrogliomas revealed 12 and 3 more tumors with mutations of CIC and FUBP1, respectively, 58% of which were predicted to result in truncations of the encoded proteins. These results suggest a critical role for these genes in the biology and pathology of oligodendrocytes.

First claim

The invention claimed is:

1. A method of identifying and treating an oligodendroglioma in a subject comprising:
detecting in a sample obtained from the subject the presence of a CIC R215W mutation, wherein the sample comprises a brain tissue suspected of being a brain tumor, or in cells or nucleic acids shed from the tumor,
identifying the subject having the mutation as having an oligodendroglioma, and
administering an anti-tumor agent to the subject identified as having an oligodendroglioma, wherein the agent is not an EGFR inhibitor.

2. A method of stratifying and treating an oligodendroglioma in a subject comprising:
detecting in a sample obtained from the subject the presence of a CIC R215W mutation, wherein the sample comprises a brain tissue suspected of being a brain tumor, or in cells or nucleic acids shed from the tumor,
stratifying the subject having the mutation by assigning the subject to a group having oligodendroglioma that is refractory to EGFR inhibitors, and
administering an anti-tumor agent to the subject stratified as having oligodendroglioma that is refractory to EGFR inhibitors, wherein the agent is not an EGFR inhibitor.

3. The method of claim 2 further comprising: assigning the patient stratified as having oligodendroglioma that is refractory to EGFR inhibitors with the mutation to a clinical trial group, wherein the clinical trial group consists of patients whose brain tumors have the mutation.

4. The method of claim 1 , wherein detecting in a sample is performed by sequencing nucleic acid in the sample.

5. The method of claim 2 , wherein detecting in a sample is performed by sequencing nucleic acid in the sample.

Assignees

• Vogelstein Bert
• Kinzler Kenneth W
• Bettegowda Chetan
• Agrawal Nishant
• Papadopoulos Nickolas
• Bigner Darell
• Yan Hai
• Mclendon Roger
• Univ Johns Hopkins
• Univ Duke

Inventors

• Vogelstein Bert
• Kinzler Kenneth W
• Bettegowda Chetan
• Agrawal Nishant
• Papadopoulos Nickolas
• Bigner Darell
• Yan Hai
• Mclendon Roger

Classifications

• C12Q2600/156

  Polymorphic or mutational markers · CPC title

• C12Q2600/112

  Disease subtyping, staging or classification · CPC title

• C12Q2600/158

  Expression markers · CPC title

• C12Q2600/118

  Prognosis of disease development · CPC title

• C12Q2600/106

  Pharmacogenomics, i.e. genetic variability in individual responses to drugs and drug metabolism · CPC title