c-Met Binding Nucleic Acid Aptamers for Cancer Diagnosis

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Solution Overview

Problem

Current methods lack effective substances to bind and neutralize the c-Met protein, which is overexpressed in various cancers, hindering diagnosis and treatment options.

Innovation Solution

Development of specific c-Met binding nucleic acid molecules, including RNA aptamers, that can bind to c-Met, neutralize its function, and serve as diagnostic and therapeutic agents.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If conventional methods are used to detect and treat c-Met-related diseases, then existing diagnostic and therapeutic options are limited, but effective binding substances to neutralize c-Met are lacking

Engineering Contradiction:
Improveeffectiveness of c-Met neutralizationVSAvoidavailability of diagnostic and therapeutic options
Core Design Contradiction:
ReliabilityVSAdaptability or versatility

Solution Approach 1:

The patent uses nucleic acid molecules (aptamers) as intermediary substances that specifically bind to c-Met protein. These aptamers act as mediators between the diagnostic/therapeutic need and the c-Met target, providing both detection capability and neutralization function. The aptamers bind to c-Met with high affinity and specificity, enabling effective neutralization of c-Met signaling pathways while serving as detectable markers for diagnosis.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Adaptability or versatility

If no specific c-Met binding substance is available, then diagnosis and treatment of c-Met-related diseases are hindered, but developing such substances requires identification of effective binding molecules

Engineering Contradiction:
Improvediagnostic and treatment optionsVSAvoididentification of effective binding substances
Core Design Contradiction:
Adaptability or versatilityVSDifficulty of detecting and measuring

Solution Approach 1:

The patent employs aptamer selection methodologies where nucleic acid libraries are subjected to systematic evolution of ligands by exponential enrichment (SELEX) processes. The aptamers self-select and self-optimize their binding affinity and specificity for c-Met through iterative rounds of selection and amplification. This self-service approach enables the identification of high-affinity binding molecules without requiring complex external screening mechanisms.

Inventive Principle:
Principle #25Self-service

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

These nucleic acid molecules effectively inhibit c-Met function, enabling early diagnosis and treatment of c-Met-related diseases, including cancer, by specifically binding to c-Met and inhibiting its signaling pathways.

Implementation Method 1

a nucleic acid molecule for use in the treatment of a disease in which c-Met is involved... capable of binding to c-Met... neutralizing the action of c-Met

Methodology Applied
Scientific EffectMolecular recognition and binding:

Data Source

PatentUS8822667B2Nucleic acid molecule capable of binding to c-Met and use thereof
Publication Date: 2014.09.02 NEC SOLUTION INNOVATORS LTD
  • US8822667B2 patent drawing
  • US8822667B2 patent drawing
  • US8822667B2 patent drawing

AI summary

The present invention provides a nucleic acid molecule capable of binding to c-Met as a substance that can be used for clarification of the pathogenic mechanism of diseases caused by c-Met, diagnosis and treatment of the diseases, and the like, and also the use thereof. The c-Met binding nucleic acid molecule of the present invention is any one of the following nucleic acid molecules (A1), (A2), (B1), and (B2).(A1) a nucleic acid molecule including the base sequence of any one of SEQ ID NOs: 1 to 38(A2) a nucleic acid molecule that is capable of binding to c-Met and includes a base sequence obtained by substitution, deletion, addition, and/or insertion of one or more bases in the base sequence of any one of SEQ ID NOs: 1 to 38(B1) a nucleic acid molecule including the base sequence of any one of SEQ ID NOs: 39 to 76(B2) a nucleic acid molecule that is capable of binding to c-Met and includes a base sequence obtained by substitution, deletion, addition, and/or insertion of one or more bases in the base sequence of any one of SEQ ID NOs: 39 to 76.