Gene defects and mutant alk kinase in human solid tumors
US-2016186268-A1 · Jun 30, 2016 · US
US10870892B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10870892-B2 |
| Application number | US-201815973718-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 8, 2018 |
| Priority date | Apr 14, 2006 |
| Publication date | Dec 22, 2020 |
| Grant date | Dec 22, 2020 |
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Novel gene deletions and translocations involving chromosome 2 resulting in fusion proteins combining part of Anaplastic Lymphoma Kinase (ALK) kinase with part of a secondary protein have been identified herein in human solid tumors, e.g. non-small cell lung carcinoma (NSCLC). Secondary proteins include Echinoderm Microtubule-Associated Protein-Like 4 (EML-4) and TRK-Fusion Gene (TFC). The EML4-ALK fusion protein, which retains ALK tyrosine kinase activity, was confirmed to drive the proliferation and survival of NSCLC characterized by this mutation. The invention therefore provides, in part, isolated polynucleotides and vectors encoding the disclosed mutant ALK kinase polypeptides, probes for detecting it, isolated mutant polypeptides, recombinant polypeptides, and reagents for detecting the fusion and truncated polypeptides. The disclosed identification of this new fusion protein enables methods for screening for compounds that inhibit the proteins, and methods for inhibiting the progression of a cancer characterized by the mutant polynucleotides or polypeptides.
Opening claim text (preview).
What is claimed is: 1. A composition, comprising a biological sample from a patient having lung cancer, and a reagent that detects a mutant Anaplastic Lymphoma Kinase (ALK) polypeptide, wherein the mutant ALK polypeptide has ALK kinase activity and is an Echinoderm Microtubule-Associated Protein-Like 4 (EML4)-ALK fusion polypeptide comprising an amino acid sequence having at least 95% identity to an amino acid sequence which comprises residues 1-222 of SEQ ID NO: 3 and residues 1116-1383 of SEQ ID NO: 5, and wherein the reagent comprises an antibody that binds to the mutant ALK polypeptide. 2. The composition of claim 1 , wherein said lung cancer is non-small cell lung cancer (NSCLC). 3. The composition of claim 1 , wherein said biological sample is a serum, pleural effusion, or tissue biopsy sample. 4. The composition of claim 1 , wherein the sample is a paraffin-embedded lung tissue sample comprising tumor cells. 5. The composition of claim 1 , wherein the antibody is conjugated with a detectable label. 6. The composition of claim 1 , wherein said mutant ALK polypeptide comprises residues 1116-1383 of SEQ ID NO: 5. 7. A composition comprising a biological sample from a patient having lung cancer, and a reagent that detects a mutant ALK polypeptide, wherein the mutant ALK polypeptide has ALK kinase activity and is an EML4-ALK fusion polypeptide comprising an amino acid sequence having at least 95% identity to SEQ ID NO: 1 or SEQ ID NO: 18, and wherein the reagent comprises an antibody that binds to the mutant ALK polypeptide. 8. The composition of claim 7 , wherein said lung cancer is non-small cell lung cancer (NSCLC). 9. The composition of claim 7 , wherein said biological sample is a serum, pleural effusion, or tissue biopsy sample. 10. The composition of claim 7 , wherein the sample is a paraffin-embedded lung tissue sample comprising tumor cells. 11. The composition of claim 7 , wherein the antibody is conjugated with a detectable label. 12. The composition of claim 7 , wherein said mutant ALK polypeptide comprises residues 1116-1383 of SEQ ID NO: 5.
involving compounds serving as markers for tumours, cancers or neoplasias, e.g. cellular determinants, receptors, heat shock/stress proteins, A-protein, oligosaccharides or metabolites · CPC title
of the lungs · CPC title
for cancer (immunoassay for cancer G01N33/575) · CPC title
from mammals · CPC title
transferring phosphorus containing groups, e.g. kinases (2.7) · CPC title
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