Ezrin assay method for the in vitro diagnosis of colorectal cancer

US9890196B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9890196-B2
Application numberUS-201213712340-A
CountryUS
Kind codeB2
Filing dateDec 12, 2012
Priority dateJul 19, 2007
Publication dateFeb 13, 2018
Grant dateFeb 13, 2018

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A method for the in vitro diagnosis of colorectal cancer by determining the presence of the Ezrin tumor marker in a biological sample taken from a patient suspected of having colorectal cancer using at least one anti-Ezrin monoclonal antibody directed against an Ezrin epitope chosen from the epitopes of sequence SEQ ID No.1, SEQ ID No.2, SEQ ID No.3, SEQ ID No.4+SEQ ID No.5, SEQ ID No.6+SEQ ID No.7 and SEQ ID No.8. Said method can be used for early diagnosis, screening, therapeutic follow-up and prognosis, and also for relapse diagnosis in relation to colorectal cancer.

First claim

Opening claim text (preview).

The invention claimed is: 1. A peptide comprising an amino acid sequence having at least 85% sequence identity with the epitope of SEQ ID No.4+SEQ ID No.5 or SEQ ID No.6+SEQ ID No.7, wherein (i) the peptide has no more than 20 amino acid residues between SEQ ID No.4 and SEQ ID No.5 or between SEQ ID No.6 and SEQ ID No.7, and (ii) the peptide has no more than 10 additional amino acid residues on each side of the amino acid sequence. 2. The peptide of claim 1 , wherein the amino acid sequence has at least 90% sequence identity with the epitope of SEQ ID No.4+SEQ ID No5 or SEQ ID No.6+SEQ ID No.7. 3. The peptide of claim 1 , wherein the peptide comprises the epitope of SEQ ID No.4+SEQ ID No.5. 4. The peptide of claim 1 , wherein the peptide comprises the epitope of SEQ ID No.6+SEQ ID No.7. 5. A peptide comprising the epitope of SEQ ID No.2, SEQ ID No.3, SEQ ID No.4+SEQ ID No.5, SEQ ID No.6+SEQ ID No.7, or SEQ ID No.8, having at least one and no more than two heterologous amino acid additions, conservative substitutions, or internal deletions as compared with Swiss Prot No. P15311, wherein (i) the peptide has no more than 20 amino acid residues between SEQ ID No.4 and SEQ ID No.5 or between SEQ ID No.6 and SEQ ID No.7 when present in the peptide, and (ii) the peptide has no more than 10 additional amino acid residues on each side of the epitope. 6. The peptide of claim 5 , wherein the peptide has at least one and no more than two conservative amino acid substitutions. 7. The peptide of claim 5 , wherein the peptide has at least one and no more than two heterologous amino acid additions. 8. The peptide of claim 5 , wherein the peptide has at least one and no more than two internal amino acid deletions. 9. A peptide comprising the amino acid sequence of SEQ ID No.2, SEQ ID No.3, or SEQ ID No.8, having at least one and no more than two heterologous amino acid additions, conservative substitutions, or internal deletions as compared with Swiss Prot No. P15311, wherein the peptide has no more than 10 additional amino acid residues on each side of the amino acid sequence. 10. A peptide comprising the amino acid sequence of SEQ ID No.1, having at least one and no more than two heterologous amino acid additions or conservative substitutions as compared with Swiss Prot No. P15311, wherein the peptide has no more than the 10 additional amino acid residues on each side of the amino acid sequence. 11. The peptide of claim 9 , comprising the amino acid sequence of SEQ ID No.2, having the at least one and no more than two heterologous amino acid additions, conservative substitutions, or internal deletions as compared with Swiss Prot No. P15311, wherein the peptide has no more than the 10 additional amino acid residues on each side of the amino acid sequence. 12. The peptide of claim 9 , comprising the amino acid sequence of SEQ ID No.3, having the at least one and no more than two heterologous amino acid additions, conservative substitutions, or internal deletions as compared with Swiss Prot No. P15311, wherein the peptide has no more than the 10 additional amino acid residues on each side of the amino acid sequence. 13. The peptide of claim 9 , comprising the amino acid sequence of SEQ ID No.8, having the at least one and no more than two heterologous amino acid additions, conservative substitutions, or internal deletions as compared with Swiss Prot No. P15311, wherein the peptide has no more than the 10 additional amino acid residues on each side of the amino acid sequence.

Assignees

Inventors

Classifications

  • of the large intestine, e.g. colon, rectum or anus · CPC title

  • involving compounds localised on the membrane of tumour or cancer cells · CPC title

  • Assays involving receptors, cell surface antigens or cell surface determinants · CPC title

  • C07K7/08Primary

    having 12 to 20 amino acids (gastrins C07K14/595; somatostatins C07K14/655; melanotropins C07K14/68) · CPC title

  • Physics · mapped topic

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What does patent US9890196B2 cover?
A method for the in vitro diagnosis of colorectal cancer by determining the presence of the Ezrin tumor marker in a biological sample taken from a patient suspected of having colorectal cancer using at least one anti-Ezrin monoclonal antibody directed against an Ezrin epitope chosen from the epitopes of sequence SEQ ID No.1, SEQ ID No.2, SEQ ID No.3, SEQ ID No.4+SEQ ID No.5, SEQ ID No.6+SEQ ID …
Who is the assignee on this patent?
Biomerieux Sa, Centre Nat Rech Scient, Inst Curie, and 1 more
What technology area does this patent fall under?
Primary CPC classification G01N33/57535. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue Feb 13 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). 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).