Compositions and methods for the treatment of tumor hematopoietic origin

US2017362318A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2017362318-A1
Application numberUS-201715406583-A
CountryUS
Kind codeA1
Filing dateJan 13, 2017
Priority dateMay 8, 2002
Publication dateDec 21, 2017
Grant date

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  1. Title

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  2. Abstract

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  5. First independent claim

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  7. Citations and related patents

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Abstract

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The present invention is directed to compositions of matter useful for the treatment of hematopoietic tumor in mammals and to methods of using those compositions of matter for the same.

First claim

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What is claimed is: 1 . Isolated nucleic acid having a nucleotide sequence that has at least 80% nucleic acid sequence identity to: (a) a DNA molecule encoding the amino acid sequence selected from the group consisting of the amino acid sequence shown in FIG. 2 (SEQ ID NO: 2), FIG. 4 (SEQ ID NO: 4), FIG. 6 (SEQ ID NO: 6), and FIG. 8 (SEQ ID NO: 8); (b) a DNA molecule encoding the amino acid sequence selected from the group consisting of the amino acid sequence shown in FIG. 2 (SEQ ID NO: 2), FIG. 4 (SEQ ID NO: 4), FIG. 6 (SEQ ID NO: 6), and FIG. 8 (SEQ ID NO: 8), lacking its associated signal peptide; (c) a DNA molecule encoding an extracellular domain of the polypeptide having the amino acid selected from the group consisting of the amino acid sequence shown in FIG. 2 (SEQ ID NO: 2), FIG. 4 (SEQ ID NO: 4), FIG. 6 (SEQ ID NO: 6) and FIG. 8 (SEQ ID NO: 8), with its associated signal peptide: (d) a DNA molecule encoding an extracellular domain of the polypeptide having the amino acid selected from the group consisting of the amino acid sequence show n in FIG. 2 (SEQ ID NO: 2), FIG. 4 (SEQ ID NO: 4), FIG. 6 (SEQ ID NO: 6) and FIG. 8 (SEQ ID NO: 8). lacking its associated signal peptide; (e) the nucleotide sequence selected from the group consisting of the nucleotide sequence shown in FIG. 1 (SEQ ID NO: 1), FIG. 3 (SEQ ID NO :3), FIG. 5 (SEQ ID NO: 5) and FIG. 7 (SEQ ID NO: 7); (f) the full-length coding region of the nucleotide sequence selected from the group consisting of the nucleotide sequence shown in FIG. 1 (SEQ ID NO: 1), FIG. 3 (SEQ ID NO: 3), FIG. 5 (SEQ ID NO: 5) and FIG. 7 (SEQ ID NO: 7); or (g) the complement of (a), (b), (c), (d), (e) or (f). 2 . Isolated nucleic acid having: (a) a nucleotide sequence that encodes the amino acid sequence selected from the group consisting of the amino acid sequence shown in FIG. 2 (SEQ ID NO: 2), FIG. 4 (SEQ ID NO: 4), FIG. 6 (SEQ ID NO: 6) and FIG. 8 (SEQ ID NO: 8); (b) a nucleotide sequence that encodes the amino acid sequence selected from the group consisting of the amino acid sequence shown in FIG. 2 (SEQ ID NO: 2), FIG. 4 (SEQ ID NO: 4), FIG. 6 (SEQ ID NO: 6) and FIG. 8 (SEQ ID NO: 8), lacking its associated signal peptide; (c) a nucleotide sequence that encodes an extracellular domain of the polypeptide having the amino acid selected from the group consisting of the amino acid sequence show n in FIG. 2 (SEQ ID NO: 2), FIG. 4 (SEQ ID NO: 4), FIG. 6 (SEQ ID NO: 6) and FIG. 8 (SEQ ID NO: 8) with its associated signal peptide; (d) a nucleotide sequence that encodes an extracellular domain of the poly peptide having the amino acid selected from the group consisting of the amino acid sequence show n in FIG. 2 (SEQ ID NO: 2), FIG. 4 (SEQ ID NO: 4), FIG. 6 (SEQ ID NO: 6) and FIG. 8 (SEQ ID NO: 8), lacking its associated signal peptide; (e) the nucleotide sequence selected from the group consisting of the nucleotide sequence shown in FIG. 1 (SEQ ID NO: 1), FIG. 3 (SEQ ID NO: 3), FIG. 5 (SEQ ID NO: 5) and FIG. 7 (SEQ ID NO: 7); (f) the full-length coding region of the nucleotide sequence selected from the group consisting of the nucleotide sequence shown in FIG. 1 (SEQ ID NO: 1), FIG. 3 (SEQ ID NO:3), FIG. 5 (SEQ ID NO: 5) and FIG. 7 (SEQ ID NO: 7); or (g) the complement of (a), (b), (c), (d), (e) or (f). 3 . Isolated nucleic acid that hybridizes to: (a) a nucleic acid that encodes the amino acid sequence selected from the group consisting of the amino acid sequence shown in FIG. 2 (SEQ ID NO: 2), FIG. 4 (SEQ ID NO: 4), FIG. 6 (SEQ ID NO: 6) and FIG. 8 (SEQ ID NO: 8); (b) a nucleic acid that encodes the amino acid sequence selected from the group consisting of the amino acid sequence shown in FIG. 2 (SEQ ID NO: 2), FIG. 4 (SEQ ID NO: 4), FIG. 6 (SEQ ID NO: 6) and FIG. 8 (SEQ ID NO: 8), lacking its associated signal peptide; (c) a nucleic acid that encodes an extracellular domain of the polypeptide having the amino acid sequence selected from the group consisting of the amino acid sequence shown in FIG. 2 (SEQ ID NO: 2), FIG. 4 (SEQ ID NO: 4), FIG. 6 (SEQ ID NO: 6) and FIG. 8 (SEQ ID NO: 8), with its associated signal peptide; (d) a nucleic acid that encodes an extracellular domain of the polypeptide having the amino acid sequence selected from the group consisting of the amino acid sequence shown in FIG. 2 (SEQ ID NO: 2), FIG. 4 (SEQ ID NO: 4), FIG. 6 (SEQ ID NO: 6) and FIG. 8 (SEQ ID NO: 8), lacking its associated signal peptide; (e) the nucleotide sequence selected from the group consisting of the nucleotide sequence shown in FIG. 1 (SEQ ID NO: 1), FIG. 3 (SEQ ID NO:3), FIG. 5 (SEQ ID NO: 5) and FIG. 7 (SEQ ID NO: 7); (f) the full-length coding region of the nucleotide sequence selected from the group consisting of the nucleotide sequence shown in FIG. 1 (SEQ ID NO: 1), FIG. 3 (SEQ ID NO:3), FIG. 5 (SEQ ID NO: 5) and FIG. 7 (SEQ ID NO: 7); or (g) the complement of (a), (b), (c), (d), (e) or (f). 4 . The nucleic acid of claim 3 , wherein the hybridization occurs under stringent conditions. 5 . The nucleic acid of claim 3 which is at least about 5 nucleotides in length. 6 . An expression vector comprising the nucleic acid of claim 1 , 2 or 3 . 7 . The expression vector of claim 6 , wherein said nucleic acid is operably linked to control sequences recognized by a host cell transformed with the vector. 8 . A host cell comprising the expression vector of claim 7 . 9 . The host cell of claim 8 which is a CHO cell, an E. coli cell or a yeast cell. 10 . A process for producing a polypeptide comprising culturing the host cell of claim 8 under conditions suitable for expression of said polypeptide and recovering said polypeptide from the cell culture. 11 . An isolated polypeptide having at least 80% amino acid sequence identity to: (a) the polypeptide having the amino acid sequence selected from the group consisting of the amino acid sequence shown in FIG. 2 (SEQ ID NO: 2), FIG. 4 (SEQ ID NO: 4), FIG. 6 (SEQ ID NO: 6) and FIG. 8 (SEQ ID NO: 8); (b) the polypeptide having the amino acid sequence selected from the group consisting of the amino acid sequence shown in FIG. 2 (SEQ ID NO: 2), FIG. 4 (SEQ ID NO: 4), FIG. 6 (SEQ ID NO: 6) and FIG. 8 (SEQ ID NO: 8), lacking its associated signal peptide; (c) an extracellular domain of the polypeptide having the amino acid sequence selected from the group consisting of the amino acid sequence shown in FIG. 2 (SEQ ID NO: 2), FIG. 4 (SEQ ID NO: 4), FIG. 6 (SEQ ID NO: 6) and FIG. 8 (SEQ ID NO: 8), with its associated signal peptide; (d) an extracellular domain of the polypeptide having the amino acid sequence selected from the group consisting of the amino acid sequence shown in FIG. 2 (SEQ ID NO: 2), FIG. 4 (SEQ ID NO: 4), FIG. 6 (SEQ ID NO: 6) and FIG. 8 (SEQ ID NO: 8), lacking its associated signal peptide; (e) a polypeptide encoded by the nucleotide sequence selected from the group consisting of the nucleotide sequence shown in FIG. 1 (SEQ ID NO: 1), FIG. 3 (SEQ ID NO:3), FIG. 5 (SEQ ID NO: 5) and FIG. 7 (SEQ ID NO: 7); or (f) a polypeptide encoded by the full-length coding region of the nucleotide sequence selected from the group consisting of the nucleotide sequence shown in FIG. 1 (SEQ ID NO: 1), FIG. 3 (SEQ ID NO:3), FIG. 5 (SEQ ID NO: 5) and FIG. 7 (SEQ ID NO: 7). 12 . An isolated polypeptide having: (a) the amino acid sequence selected from the group consisting of the amino acid sequence shown in FIG. 2 (SEQ ID NO: 2), FIG. 4 (SEQ ID NO: 4), FIG. 6

Assignees

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Classifications

  • specific for metastasis · CPC title

  • Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

  • specific for leukemia · CPC title

  • Antineoplastic agents · CPC title

  • for cancer · CPC title

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What does patent US2017362318A1 cover?
The present invention is directed to compositions of matter useful for the treatment of hematopoietic tumor in mammals and to methods of using those compositions of matter for the same.
Who is the assignee on this patent?
Genentech Inc
What technology area does this patent fall under?
Primary CPC classification C07K16/2803. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Dec 21 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).