Supplementary Figure 6 from Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer

Antje Neeb; Ines Figueiredo; Denisa Bogdan; Laura Cato; Jutta Stober; Juan M. Jiménez‐Vacas; Victor Gourain; Irene Lee; Rebecca Seeger; Claudia Muhle‐Goll; Bora Gürel; Jonathan Welti; Daniel Nava Rodrigues; Jan Rekowski; Xintao Qiu; Yija Jiang; Patrizio Di Micco; Borja Mateos; Stasė Bielskutė; Ruth Riisnaes; Ana Ferreira; Susana Miranda; Mateus Crespo; Lorenzo Buroni; Jian Ning; Suzanne Carreira; Stefan Bräse; Nicole Jung; Simone Gräßle; Amanda Swain; Xavier Salvatella; Stephen R. Plymate; Bissan Al‐Lazikani; Henry W. Long; Wei Yuan; Myles Brown; Andrew C.B. Cato; Johann S. de Bono; Adam Sharp

doi:10.1158/1535-7163.25965016

Abstract

In-vivo treatment of patient derived model of lethal prostate cancer demonstrates Thio-2 to be well tolerated with associated impact on AR signaling and growth.

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Neeb et al. (2024) studied this question.

synapsesocial.com/papers/68e664bab6db6435875f16fe https://doi.org/10.1158/1535-7163.25965016

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Supplementary Figure 6 from Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer

Abstract

Discussion

Cite This Study

Supplementary Figure 6 from Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer

Abstract

Discussion

Cite This Study

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