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New Potent Inhibitor of Transforming Growth Factor-Beta (TGFβ) Signaling that is Efficacious against Microsatellite Stable Colorectal Cancer Metastasis in Combination with Immune Checkpoint Therapy in Mice.

Authors :
Tauriello DVF
Sancho E
Byrom D
Sanchez-Zarzalejo C
Salvany M
Henriques A
Palomo-Ponce S
Sevillano M
Hernando-Momblona X
Matarin JA
Ramos I
Ruano I
Prats N
Batlle E
Riera A
Source :
ACS pharmacology & translational science [ACS Pharmacol Transl Sci] 2024 Oct 01; Vol. 8 (1), pp. 97-112. Date of Electronic Publication: 2024 Oct 01 (Print Publication: 2025).
Publication Year :
2024

Abstract

Blockade of the TGFβ signaling pathway has emerged from preclinical studies as a potential treatment to enhance the efficacy of immune checkpoint inhibition in advanced colorectal cancer (CRC) and several other types of cancer. However, clinical translation of first-generation inhibitors has shown little success. Here, we report the synthesis and characterization of HYL001, a potent inhibitor of TGFβ receptor 1 (ALK5), that is approximately 9 times more efficacious than the structurally related compound galunisertib, while maintaining a favorable safety profile. HYL001 in combination with immune checkpoint blockade (anti-PD1) eradicates liver metastases generated in mice by microsatellite stable, aggressive colorectal cancer tumors at doses where galunisertib is ineffective.<br />Competing Interests: The authors declare the following competing financial interest(s): DT, DB, JM, AR, and EB hold a patent on the synthesis and use of HYL001. E.B. is author in a patent describing bispecific antibodies to target cancer stem cells. The laboratory of E.B. has received research funding from MERUS and INCYTE. E.B. has received honoraria for consulting from Genentech.<br /> (© 2024 The Authors. Published by American Chemical Society.)

Details

Language :
English
ISSN :
2575-9108
Volume :
8
Issue :
1
Database :
MEDLINE
Journal :
ACS pharmacology & translational science
Publication Type :
Academic Journal
Accession number :
39816803
Full Text :
https://doi.org/10.1021/acsptsci.4c00374