Squamous Cell Carcinoma Subtype Classification via Gene Expression

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Solution Overview

Problem

Current methods lack a reliable and precise way to evaluate the efficacy of chemoradiotherapy for squamous cell carcinoma, particularly in identifying sensitive subtypes and predicting prognosis, due to insufficient analysis of esophageal squamous cell carcinoma samples.

Innovation Solution

An unsupervised cluster analysis based on comprehensive gene expression profiles identifies subtypes correlated with treatment prognoses, focusing on the SIM2 and FOXE1 genes and their co-expressed genes to determine chemoradiotherapy sensitivity, enabling high-precision evaluation of chemoradiotherapy efficacy.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If conventional gene expression analysis methods are used for squamous cell carcinoma, then general cancer treatment guidelines can be followed, but the precision of chemoradiotherapy efficacy evaluation is insufficient

Engineering Contradiction:
Improvechemoradiotherapy efficacy evaluation precisionVSAvoidprognosis prediction reliability
Core Design Contradiction:
Measurement precisionVSReliability

Solution Approach 1:

The invention segments squamous cell carcinoma into five distinct molecular subtypes (subtype-1 through subtype-5) based on gene expression profiles. This segmentation allows for precise identification of chemoradiotherapy-sensitive subtypes (subtype-2, subtype-3, subtype-5) versus resistant subtypes (subtype-1, subtype-4), thereby improving both measurement precision of treatment efficacy and reliability of prognosis prediction.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The invention changes the evaluation parameter from general cancer treatment response to specific gene expression profile analysis. By measuring expression levels of specific genes (including SIM2 and its co-expressed genes, as well as FOXE1 and its co-expressed genes), the method achieves high-precision evaluation of chemoradiotherapy efficacy that was not possible with conventional approaches.

Inventive Principle:
Principle #35Parameter changes

2Measurement precision

If comprehensive gene expression profile analysis is performed to identify subtypes, then chemoradiotherapy sensitivity can be accurately predicted, but the complexity of the evaluation method increases

Engineering Contradiction:
Improvechemoradiotherapy sensitivity prediction accuracyVSAvoidevaluation method complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The invention extracts specific key genes and gene groups from the comprehensive gene expression profile that are most predictive of chemoradiotherapy response. By focusing on specific genes (SIM2, FOXE1 and their co-expressed genes) rather than analyzing all genes equally, the method maintains high prediction accuracy while reducing evaluation complexity.

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The invention performs partial analysis by selecting and analyzing only the most relevant gene groups associated with chemoradiotherapy sensitivity. Rather than requiring comprehensive analysis of all possible genes, the method focuses on specific gene groups that provide sufficient predictive power, thereby balancing accuracy with practical feasibility.

Inventive Principle:
Principle #16Partial or excessive action

Data Source

PatentUS10969390B2Method for evaluating efficacy of chemoradiotherapy against squamous cell carcinoma
Publication Date: 2021.04.06 SYSMEX CORP
  • US10969390B2 patent drawing
  • US10969390B2 patent drawing
  • US10969390B2 patent drawing

AI summary

A method for evaluating an efficacy of a chemoradiotherapy against squamous cell carcinoma comprises the following steps (a) to (c):(a) detecting an expression level of at least one gene selected from a SIM2 gene and genes co-expressed with the SIM2 gene in a squamous cell carcinoma specimen isolated from a subject;(b) comparing the expression level detected in the step (a) with a reference expression level of the corresponding gene; and(c) determining that an efficacy of a chemoradiotherapy against squamous cell carcinoma in the subject is high if the expression level in the subject is higher than the reference expression level as a result of the comparison in the step (b).