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September 16, 2024

Supplementary Fig. 3 from MEK inhibition sensitizes pancreatic cancer to STING agonism by tumor-cell intrinsic amplification of type I interferon signaling

Razmik Ghukasyan Keke Liang Kevin Chau Luyi Li Charlotte Chan Evan R. Abt Thuc Le Joon Y. Park Nanping Wu Alykhan Premji Robert Damoiseaux Tony Luu Amanda Labora Khalid Rashid Jason M. Link Caius G. Radu Timothy R. Donahue

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Abstract

Supplementary Fig. 3 MEK inhibition amplifies STING-induced transcription of IFNB1, IL-6, and TNFA in multiple PDAC cell lines.

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Cite This Study

Ghukasyan et al. (2024) studied this question.

synapsesocial.com/papers/68e586c1b6db6435875237bd https://doi.org/10.1158/1078-0432.27031738

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Supplementary Fig. 3 from MEK inhibition sensitizes pancreatic cancer to STING agonism by tumor-cell intrinsic amplification of type I interferon signaling2024
2Supplementary Fig. 2 from MEK inhibition sensitizes pancreatic cancer to STING agonism by tumor-cell intrinsic amplification of type I interferon signaling2024
3Supplementary Fig. 2 from MEK inhibition sensitizes pancreatic cancer to STING agonism by tumor-cell intrinsic amplification of type I interferon signaling2024
4Supplementary Fig. 5 from MEK inhibition sensitizes pancreatic cancer to STING agonism by tumor-cell intrinsic amplification of type I interferon signaling2024
5Supplementary Fig. 5 from MEK inhibition sensitizes pancreatic cancer to STING agonism by tumor-cell intrinsic amplification of type I interferon signaling2024