Engineered microorganisms for detection of diseased cells
US-2024118283-A1 · Apr 11, 2024 · US
US12282020B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12282020-B2 |
| Application number | US-202016939154-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 27, 2020 |
| Priority date | Jan 30, 2018 |
| Publication date | Apr 22, 2025 |
| Grant date | Apr 22, 2025 |
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The present invention relates to the use of BMW Rep-protein as a biomarker for colon cancer.
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What is claimed is: 1. A method for providing a diagnosis or predisposition for colorectal cancer (CRC) in a subject, comprising: obtaining a sample from a subject; detecting whether a Bovine Meat and Milk Factor Group 1 (BMMF1) Rep Protein is present in the sample by contacting the sample with one or more antibodies selected from the group consisting of Ab 1-5 (DSM ACC3327), Ab 5-2 (DSM ACC3328) and Ab 3-6 (DSM ACC3329) and detecting binding between BMMF1 and said one or more antibodies; and providing a diagnosis or predisposition for CRC to the subject when the presence of BMMF1 in the sample is detected. 2. The method of claim 1 , wherein the sample from the subject is selected from the group consisting of a cancerous colon tissue, peripheral tissue surrounding the cancerous colon tissue and benign colon polyps. 3. The method of claim 1 , wherein additionally CD68 positive cells are detected in the sample by an anti-CD68 antibody. 4. A method for providing a prognostic score on a CRC patient's survival time, comprising: a) obtaining a sample from peritumoral regions of CRC patients; b) contacting the sample with one or more antibodies selected from the group consisting of Ab 1-5 (DSM ACC3327), Ab 5-2 (DSM ACC3328) and Ab 3-6 (DSM ACC3329), c) staining the sample to visualize binding between Rep protein and the one or more antibodies; d) detecting Rep protein in the stained sample by observing the visualized binding; e) quantifying the detected Rep protein by: i) determining for each antibody the percentage of stained cells, and ii) measuring the staining intensity; f) calculating an immunohistological score based on the quantified Rep protein; and g) correlating the calculated immunohistological score to a CRC-specific patient's survival time.
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