US2005186610A1PendingUtilityA1
Breast cancer related protein, gene encoding the same, and method of diagnosing breast cancer using the protein and gene
Priority: Feb 20, 2004Filed: Feb 18, 2005Published: Aug 25, 2005
Est. expiryFeb 20, 2024(expired)· nominal 20-yr term from priority
G01N 33/57515C07H 21/04C07K 14/47C12Q 1/6886C12Q 2600/158
50
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Claims
Abstract
An isolated protein having an amino acid sequence of SEQ ID No. 4 and having an activity inducing apoptosis, and a gene encoding the same are provided. Also, a microarray having a substrate on which the gene or fragment thereof is immobilized is provided. Also, a method of diagnosing breast cancer using an antibody specifically binding to the protein and a method of diagnosing breast cancer by determining whether the gene is expressed in a cell or not, are provided.
Claims
exact text as granted — not AI-modified1 . An isolated protein comprising:
an amino acid sequence of SEQ ID No. 4, wherein the protein is specifically expressed in a breast cancer cell.
2 . The isolated protein of claim 1 , which is associated with apoptosis.
3 . The isolated protein of claim 1 , which increases expression p53, p21, or a combination comprising one or more of the foregoing proteins in a cell.
4 . The isolated protein of claim 1 , further comprising a heterologous polypeptide fused thereto.
5 . A method of detecting the presence or absence of a breast cancer in a test sample, the method comprising:
contacting an isolated anti-BCRP antibody with a polypeptide sample isolated from breast tissue from a human, wherein the anti-BCRP antibody specifically interacts with the polypeptide of SEQ ID NO:1; and detecting any anti-BCRP-antibody-protein complexes that are formed, wherein an increase in anti-BCRP-antibody-protein complexes compared to a polypeptide sample isolated from normal breast cells indicates the presence of the breast cancer in the test sample.
6 . The method of claim 4 , wherein the increase in anti-BCRP-antibody protein complexes compared to a polypeptide sample isolated from normal breast cells is about a 3% increase.
7 . A recombinant expression vector comprising:
a polynucleotide encoding a protein of claim 1 operably linked to expression control sequences.
8 . The recombinant expression vector of claim 7 , wherein the polynucleotide encoding a protein of claim 1 comprises SEQ ID NO. 3.
9 . The recombinant expression vector of claim 7 , wherein the polynucleotide is operatively linked to a tag sequence.
10 . A polynucleotide or a complementary polynucleotide thereof for a diagnosis or treatment of breast cancer, comprising:
about 10 to about 100 continuous nucleotides derived from a polynucleotide having a nucleotide sequence of SEQ ID No. 3.
11 . The polynucleotide of claim 10 , further comprising about 20 to about 100 contiguous nucleotides.
12 . A microarray for the diagnosis of breast cancer, comprising:
a substrate, the substrate comprising a plurality of addresses, wherein at least one address comprises a polynucleotide according to claim 10 .
13 . A kit for the diagnosis of breast cancer, comprising:
a polynucleotide of claim 10; a reagent suitable for performing a detection method; and instructions for use thereof.
14 . A method of detecting the presence or absence of breast cancer, the method comprising
obtaining a breast tissue test sample from a subject; and determining an expression level of a protein of claim 1 in the breast tissue test sample, wherein an elevated expression level of the protein of claim 1 in the breast tissue test sample compared to an expression level of the protein of claim 1 in a sample of normal breast tissue indicates the presence of breast cancer in the breast tissue test sample.
15 . The method of claim 14 , wherein the expression level of the protein of claim 1 in the breast tissue test sample is greater than or equal to about 2-fold higher than the expression level of the protein of claim 1 in the sample of normal breast tissue.
16 . The method of claim 14 , wherein determining the expression level is determined by northern blotting or electrophoresis.
17 . The method of claim 14 , wherein determining comprises:
isolating total RNA from the breast tissue test sample; performing reverse-transcription-polymerase chain reaction on the total RNA with a primer comprising 10 or more contiguous nucleotides of SEQ ID NO. 3; and quantifying the product produced.Join the waitlist — get patent alerts
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