Fusion Molecules for Detecting Novel Cancer-Associated Genetic Lesions
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Solution Overview
Problem
Current technologies lack effective methods for identifying and targeting novel genetic lesions associated with various cancers, such as B cell cancer, lung cancer, breast cancer, ovarian cancer, and pancreatic cancer, which are characterized by complex chromosome structural aberrations.
Innovation Solution
The discovery and characterization of novel rearrangement events leading to fusion molecules, including fragments of genes like FGFR3 and TACC3, which are expressed in cancer tissues and can be used to develop compositions and methods for detecting, assessing, and treating cancers.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Reliability
If current technologies are used for identifying genetic lesions, then existing detection methods can be applied, but they lack effectiveness for novel genetic lesions associated with cancers
Solution Approach 1:
The patent segments the detection approach by identifying specific fusion molecules (e.g., FGFR3-TACC3, TRIM24-BRAF, CNTL-RAF1) as distinct targets. Each fusion molecule represents a segmented genetic lesion that can be detected independently, allowing the detection system to handle novel genetic lesions that differ from conventional cancer markers.
Solution Approach 2:
The patent uses fusion molecules as intermediary targets that bridge the gap between conventional detection methods and novel genetic lesions. By detecting the fusion event itself (the intermediary) rather than requiring direct detection of the underlying chromosomal aberration, the system achieves effectiveness for novel lesions while using established molecular detection technologies.
2Ease of manufacture
If fusion molecules are used to target cancers, then therapeutic interventions can be developed, but the complexity of identifying and characterizing novel rearrangement events increases
Solution Approach 1:
The patent performs preliminary identification and characterization of fusion molecules (FGFR3-TACC3, TRIM24-BRAF, CNTL-RAF1) before developing therapeutic interventions. By pre-characterizing these fusion events and their association with specific cancers, the patent simplifies subsequent drug development efforts, as the targets are already defined and validated.
Solution Approach 2:
The patent identifies fusion molecules that have universal applicability across multiple cancer types (B cell cancer, lung cancer, breast cancer, ovarian cancer, pancreatic cancer). This multi-functionality allows a single detection and treatment approach to address novel genetic lesions in various cancers, reducing the overall complexity of developing cancer therapies.
Data Source
AI summary
Novel fusion molecules and uses are disclosed.


