Design of Potent and Selective BCL6 Transcriptional Chemical Inducers of Proximity through Linker Optimization

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Authors: Fang-Chi Chang, Veronika M. Shoba, Oleh Shyshlyk, Andrii Frolov, Daniil Skrypnik, Halyna Bubela, Yuliia Holota, Corentine M. C. Laurin, Rodrigo A. Rodriguez, C. Avery Sader, Timur Savchenko, Petro Borysko
+2 more Armand B. Cognetta, Oleksandr O. Grygorenko
Cited by: 1
References: 31

Abstract

B-cell lymphoma 6 (BCL6) is a transcriptional repressor implicated in diffuse large B-cell lymphoma and other malignancies. Conventional BCL6 inhibitors and degraders rely on loss-of-function mechanisms that may be limited by incomplete pathway suppression. Transcriptional chemical inducers of proximity (TCIPs) provide a gain-of-function alternative by redirecting transcriptional coactivators to BCL6-bound genomic loci, thereby reactivating pro-apoptotic gene expression. Here, we describe the medicinal chemistry optimization of BCL6 TCIPs through systematic linker engineering. A focused library of 66 heterobifunctional analogues derived from JQ1 and BI-3812 was evaluated for ternary complex formation, cellular potency, and selectivity. Linker rigidification and incorporation of cyclic elements significantly improved cellular selectivity, enhanced solubility, and increased the plasma exposure in mice. Computational analyses, competition experiments, and RNA sequencing indicate that the effects of the optimized analogues are driven by ternary complex formation. Together, these findings establish the linker architecture as a critical determinant of TCIP performance.

Fields of Study & Subjects

Genomics and Chromatin Dynamics Gene Regulatory Network Analysis Protein Degradation and Inhibitors

Publication details

Journal / source
Journal of Medicinal Chemistry
Publisher
American Chemical Society (ACS)
Volume
69
Issue
13
Pages
15668–15684
Publication date
25 June 2026
Language
EN