Evidence map›Paper›PMID 41950925›Full record

ArticleCell chemical biology2026

Selective degradation of TBK1 uncovers mechanistic insights into blocking ccRCC progression.

Chengheng Liao, Siying Lyu, Rebecca L Johnson, Tiantian Shang, Xiaoyu Wang, Nina Gildor, Shina Li, Noelle S Williams, Lindsey I James, Lianxin Hu and 1 more

Abstract read
In one paragraph

Article in Cell chemical biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Chengheng LiaoDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Siying LyuDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Rebecca L JohnsonDivision of Chemical Biology and Medicinal Chemistry, Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, NC, USA.
Tiantian ShangDepartment of Urology, Institute of Urologic Science and Technology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Xiaoyu WangDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Nina GildorDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Shina LiDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Noelle S WilliamsDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Lindsey I JamesDivision of Chemical Biology and Medicinal Chemistry, Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, NC, USA; Lineberger Comprehensive Cancer Center, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Lianxin HuDepartment of Urology, Institute of Urologic Science and Technology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China. Electronic address: lianxin.hu@zju.edu.cn.
Qing ZhangDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA; Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, USA. Electronic address: qing.zhang@utsouthwestern.edu.

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Deborah F. Tate · 1985 to 2026
$201.5M
Identification of DCLK2-TBK1 signaling axis as a potential therapeutic target in kidney cancerR01CA284591 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Qing Zhang · 2023 to 2026
$1.9M
NCI NIH HHS P30 CA016086NCI NIH HHS R01 CA284591
6 · The paper itself

Abstract

Clear cell renal cell carcinoma (ccRCC), the most common kidney cancer subtype, often features the inactivation of the von Hippel-Lindau (VHL) tumor suppressor, creating therapeutic vulnerabilities. Although HIF2α inhibitors have shown clinical promise, many VHL-deficient tumors remain resistant. -binding kinase 1 (TBK1) has emerged as a synthetic lethal target in this context. Here, we report UNC8209, an optimized cereblon(CRBN)-recruiting proteolysis-targeting chimera (PROTAC) that selectively and potently degrades TBK1. Compared with earlier TBK1 degraders, UNC8209 exhibits enhanced degradation efficiency and improved selectivity over off-target kinases, including IKKε. TBK1 degradation by UNC8209 suppresses proliferation in VHL-deficient ccRCC models and impairs tumor growth in vivo with minimal toxicity within a defined therapeutic window. In addition, the anti-proliferative effects of UNC8209 extend to multiple tumor types addicted to elevated TBK1 activity. Together, these findings establish UNC8209 as a selective chemical probe and support TBK1 degradation as a therapeutic strategy in TBK1-dependent cancers.

Indexed as

Antineoplastic AgentsCarcinoma, Renal CellKidney NeoplasmsProtein Kinase InhibitorsProtein Serine-Threonine KinasesAnimalsCell Line, TumorCell ProliferationDisease ProgressionHumansMiceProteolysisProteolysis Targeting ChimeraAntineoplastic AgentsProtein Kinase InhibitorsProtein Serine-Threonine KinasesProteolysis Targeting ChimeraTBK1 protein, humancancer therapeuticsccRCCcereblonPROTACtargeted protein degradationTBK1VHL

Identifiers

PMID41950925
PMCPMC13425981

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.