Compositions for detecting mutant anaplastic lymphoma kinase in lung cancer
US-2019127804-A1 · May 2, 2019 · US
US11505833B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11505833-B2 |
| Application number | US-202017102639-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 24, 2020 |
| Priority date | Apr 14, 2006 |
| Publication date | Nov 22, 2022 |
| Grant date | Nov 22, 2022 |
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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 (TFG). 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.
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What is claimed is: 1. A composition, comprising a reverse transcription DNA polymerase, and a nucleic acid reagent comprising a primer pair that hybridizes to an mRNA encoding an Echinoderm Microtubule-Associated Protein-Like 4 (EML4)-Anaplastic Lymphoma Kinase (ALK) fusion polypeptide, wherein the EML4-ALK fusion polypeptide comprises SEQ ID NO: 1 or SEQ ID NO: 18, and wherein the primer pair amplifies at least a fragment of said mRNA comprising the fusion junction. 2. The composition of claim 1 , further comprising a biological sample from a human having lung cancer. 3. The composition of claim 2 , wherein said lung cancer is non-small cell lung cancer (NSCLC). 4. The composition of claim 1 , wherein said biological sample is a serum, pleural effusion, or tissue biopsy sample. 5. The composition of claim 1 , wherein one primer of the primer pair hybridizes to exon 6 of an EML4 gene. 6. The composition of claim 1 , wherein one primer of the primer pair hybridizes to exon 13 of an EML4 gene. 7. The composition of claim 1 , wherein one primer of the primer pair hybridizes to exon 20 of an ALK gene. 8. A composition comprising a reverse transcription DNA polymerase, a biological sample from a human having lung cancer, and a nucleic acid reagent comprising a primer pair that hybridizes to a region of an mRNA encoding a polypeptide with ALK kinase activity, wherein the region consists of a nucleotide sequence coding for amino acids 234-796 of SEQ ID NO: 1. 9. The composition of claim 8 , wherein said lung cancer is non-small cell lung cancer (NSCLC). 10. The composition of claim 8 , wherein said biological sample is a serum, pleural effusion, or tissue biopsy sample.
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
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Receptor protein-tyrosine kinase (2.7.10.1) · CPC title
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Medicinal preparations containing peptides (peptides containing beta-lactam rings A61K31/00; cyclic dipeptides not having in their molecule any other peptide link than those which form their ring, e.g. piperazine-2,5-diones, A61K31/00; ergot alkaloids of the cyclic peptide type A61K31/48; containing macromolecular compounds having statistically distributed amino acid units A61K31/74; medicinal preparations containing antigens or antibodies A61K39/00; medicinal preparations characterised by the non-active ingredients, e.g. peptides as drug carriers, A61K47/00) · CPC title
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