3D Centromere Organization Analysis for Cancer Detection

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Solution Overview

Problem

Current methods lack precise understanding and effective detection of three-dimensional (3D) centromere organization in normal, immortalized, and tumor cells, which is crucial for genomic stability and cancer diagnosis.

Innovation Solution

A method using high-resolution deconvolution microscopy and 3D analysis to characterize centromere organization by measuring distances between centromeres and the nuclear center/border, enabling detection and monitoring of cancer or precancerous cells by comparing centromere organization in test cells to control cells.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If 3D analysis of centromere organization is performed to detect cancer, then detection precision is improved, but device complexity increases

Engineering Contradiction:
Improvecancer detection precisionVSAvoidanalysis system complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The nuclear space is segmented into radial zones (centromeric, intermediate, and peripheral regions) based on distance from the nuclear center. This segmentation allows quantitative characterization of centromere organization by calculating the proportion of centromeres in each zone, transforming complex 3D spatial data into measurable parameters for cancer detection

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The method transitions from 2D planar analysis to 3D radial analysis by calculating distances of centromeres from the nuclear center and border. This dimensional change enables detection of subtle organizational changes in centromere distribution that are not visible in conventional 2D microscopy, improving cancer detection precision

Inventive Principle:
Principle #17Another dimension (Dimensionality change)

2Measurement precision

If high-resolution deconvolution microscopy is used to characterize centromere organization, then measurement precision is improved, but use of energy increases

Engineering Contradiction:
Improvecentromere position measurement precisionVSAvoidmicroscopy energy consumption
Core Design Contradiction:
Measurement precisionVSUse of energy by moving object

Solution Approach 1:

The method performs preliminary computational deconvolution and 3D reconstruction during the image acquisition process, preparing the data for subsequent analysis. This preliminary processing enables precise measurement of centromere positions and radial distances without requiring additional high-energy post-processing steps

Inventive Principle:
Principle #10Preliminary action

3Measurement precision

If centromere organization is analyzed to detect early cancer stages, then detection precision is improved, but difficulty of detecting and measuring increases

Engineering Contradiction:
Improveearly cancer detection precisionVSAvoidcentromere organization measurement difficulty
Core Design Contradiction:
Measurement precisionVSDifficulty of detecting and measuring

Solution Approach 1:

The method introduces radial distance from nuclear center and border as intermediary parameters that mediate between complex 3D centromere configurations and measurable quantities. By transforming spatial arrangement into radial distance metrics and calculating proportions in radial zones, the method simplifies the measurement of centromere organization changes in early cancer stages

Inventive Principle:
Principle #24Intermediary (Mediator)

Data Source

PatentEP2066816B1Methods of detecting and monitoring cancer using 3D analysis of centromeres
Publication Date: 2014.11.12 D SIGNATURES INC
  • EP2066816B1 patent drawingFigure 1
  • EP2066816B1 patent drawingFigure 2A~2C
  • EP2066816B1 patent drawingFigure 3

AI summary

The present application relates to a method of detecting and monitoring cancer or precancer in a cell using three-dimensional analysis to assess centromere organization. In addition, the application relates to a method and system for characterizing the 3D organization of centromeres.