Evidence map›Paper›PMID 35086954›Full record

ArticleMolecular cancer therapeutics2022

Functional Genomic Identification of Predictors of Sensitivity and Mechanisms of Resistance to Multivalent Second-Generation TRAIL-R2 Agonists.

Vera Grinkevitch, Mark Wappett, Nyree Crawford, Stacey Price, Andrea Lees, Christopher McCann, Katherine McAllister, Jochen Prehn, Jamie Young, Jess Bateson and 14 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 46% of its field
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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Early Detection of Cell Death Using Transmembrane Water Exchange Magnetic Resonance Imaging.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors at 6 institutions in 4 countries.

Vera Grinkevitch *Wellcome Sanger Institute, Hinxton, Cambridge, United Kingdom.
Mark Wappett *Patrick G. Johnston Centre for Cancer Research, Queen's University, Belfast, United Kingdom.
Nyree Crawford *Patrick G. Johnston Centre for Cancer Research, Queen's University, Belfast, United Kingdom.ORCID 0000-0003-2258-4687
Stacey PriceWellcome Sanger Institute, Hinxton, Cambridge, United Kingdom.
Andrea LeesPatrick G. Johnston Centre for Cancer Research, Queen's University, Belfast, United Kingdom.ORCID 0000-0001-9736-2777
Christopher McCannPatrick G. Johnston Centre for Cancer Research, Queen's University, Belfast, United Kingdom.
Katherine McAllisterPatrick G. Johnston Centre for Cancer Research, Queen's University, Belfast, United Kingdom.
Jochen PrehnRoyal College of Surgeons Ireland, Dublin, Ireland.ORCID 0000-0003-3479-7794
Jamie YoungWellcome Sanger Institute, Hinxton, Cambridge, United Kingdom.ORCID 0000-0002-0952-2396
Jess BatesonWellcome Sanger Institute, Hinxton, Cambridge, United Kingdom.ORCID 0000-0002-7725-846X
Lewis GallagherWellcome Sanger Institute, Hinxton, Cambridge, United Kingdom.ORCID 0000-0003-2694-3157
Magali MichautDivision of Molecular Carcinogenesis, The Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID 0000-0003-2002-2277
Vivek IyerWellcome Sanger Institute, Hinxton, Cambridge, United Kingdom.
Aikaterini ChatzipliWellcome Sanger Institute, Hinxton, Cambridge, United Kingdom.
Syd BarthorpeWellcome Sanger Institute, Hinxton, Cambridge, United Kingdom.
Daniel CiznadijaChampions Oncology Inc., Rockville, Maryland.
Ido SlomaChampions Oncology Inc., Rockville, Maryland.
Amy WesaChampions Oncology Inc., Rockville, Maryland.ORCID 0000-0002-4917-5165
David A TiceOncology R&D, AstraZeneca, Gaithersburg, Maryland.
Lodewyk WesselsDivision of Molecular Carcinogenesis, The Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID 0000-0002-1656-6995
Mathew GarnettWellcome Sanger Institute, Hinxton, Cambridge, United Kingdom.
Daniel B Longley *Patrick G. Johnston Centre for Cancer Research, Queen's University, Belfast, United Kingdom.ORCID 0000-0003-2495-2033
Ultan McDermott *Wellcome Sanger Institute, Hinxton, Cambridge, United Kingdom.
Simon S McDade *Patrick G. Johnston Centre for Cancer Research, Queen's University, Belfast, United Kingdom.ORCID 0000-0002-3024-4773
Wellcome Sanger Institute · GBQueen's University Belfast · GBChampions Oncology (United States) · USOncode Institute · NLAstraZeneca (Netherlands) · NLRoyal College of Surgeons in Ireland · IE

Funding

Biotechnology and Biological Sciences Research Council BB/T002824/1Cancer Research UK 24387Cancer Research UK C11884European Research Council 319661Medical Research Council G0400302Medical Research Council MC_PC_17117Medical Research Council MR/S021205/1Wellcome Trust 110371/Z/15/Z
6 · The paper itself

Abstract

Multivalent second-generation TRAIL-R2 agonists are currently in late preclinical development and early clinical trials. Herein, we use a representative second-generation agent, MEDI3039, to address two major clinical challenges facing these agents: lack of predictive biomarkers to enable patient selection and emergence of resistance. Genome-wide CRISPR knockout screens were notable for the lack of resistance mechanisms beyond the canonical TRAIL-R2 pathway (caspase-8, FADD, BID) as well as p53 and BAX in TP53 wild-type models, whereas a CRISPR activatory screen identified cell death inhibitors MCL-1 and BCL-XL as mechanisms to suppress MEDI3039-induced cell death. High-throughput drug screening failed to identify genomic alterations associated with response to MEDI3039; however, transcriptomics analysis revealed striking association between MEDI3039 sensitivity and expression of core components of the extrinsic apoptotic pathway, most notably its main apoptotic effector caspase-8 in solid tumor cell lines. Further analyses of colorectal cell lines and patient-derived xenografts identified caspase-8 expression ratio to its endogenous regulator FLIP(L) as predictive of sensitivity to MEDI3039 in several major solid tumor types and a further subset indicated by caspase-8:MCL-1 ratio. Subsequent MEDI3039 combination screening of TRAIL-R2, caspase-8, FADD, and BID knockout models with 60 compounds with varying mechanisms of action identified two inhibitor of apoptosis proteins (IAP) that exhibited strong synergy with MEDI3039 that could reverse resistance only in BID-deleted models. In summary, we identify the ratios of caspase-8:FLIP(L) and caspase-8:MCL-1 as potential predictive biomarkers for second-generation TRAIL-R2 agonists and loss of key effectors such as FADD and caspase-8 as likely drivers of clinical resistance in solid tumors.

Indexed as

Proto-Oncogene Proteins c-bcl-2TNF-Related Apoptosis-Inducing LigandApoptosisCASP8 and FADD-Like Apoptosis Regulating ProteinCaspase 8Cell Line, TumorGenomicsHumansCASP8 and FADD-Like Apoptosis Regulating ProteinCaspase 8Proto-Oncogene Proteins c-bcl-2TNF-Related Apoptosis-Inducing Ligand

Identifiers

PMID35086954
PMCPMC7612587
OpenAlexW4210314537

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.