Protocols to evaluate mutant specificity of an oncogene-targeting siRNA using orthogonal in vitro and in vivo approaches

RNA interference (RNAi) is a promising new approach for oncogene targeting for "undruggable" targets, including KRAS. Here, we present a protocol for evaluating mutant selectivity of KRAS small interfering RNAs (siRNAs) using orthogonal in vitro and in vivo techniques. We describe steps for structural analyses of siRNA complexes, utilization of isogenic HA- and luciferase-tagged cell lines, RNA sequencing for off-target effects, and in vivo evaluation of mutant selectivity. This protocol has potential application for the development of mutant-specific siRNA molecules targeting any oncogene. For complete details on the use and execution of this protocol, please refer to Stanland et al.<sup>1</sup>.

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Publication Details

Journal
STAR Protocols
Published
2026-01-08
DOI
https://doi.org/10.1016/j.xpro.2025.104323
Primary Topic
RNA Interference and Gene Delivery
Type
article
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article

Protocols to evaluate mutant specificity of an oncogene-targeting siRNA using orthogonal in vitro and in vivo approaches

Lyla J. Stanland, Martin Egli, Alessandro Porrello, Chad V. Pecot
STAR Protocols
RNA Interference and Gene Delivery
article

Protocols to evaluate mutant specificity of an oncogene-targeting siRNA using orthogonal in vitro and in vivo approaches

Lyla J. Stanland, Martin Egli, Alessandro Porrello, Chad V. Pecot
article en

Abstract

RNA interference (RNAi) is a promising new approach for oncogene targeting for "undruggable" targets, including KRAS. Here, we present a protocol for evaluating mutant selectivity of KRAS small interfering RNAs (siRNAs) using orthogonal in vitro and in vivo techniques. We describe steps for structural analyses of siRNA complexes, utilization of isogenic HA- and luciferase-tagged cell lines, RNA sequencing for off-target effects, and in vivo evaluation of mutant selectivity. This protocol has potential application for the development of mutant-specific siRNA molecules targeting any oncogene. For complete details on the use and execution of this protocol, please refer to Stanland et al.<sup>1</sup>.

STAR ProtocolsVol. 7(1)
Vanderbilt University (US), Tenax Therapeutics (United States) (US)
Openalex Percentile: Top 94%
RNA Interference and Gene Delivery
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