Evidence map›Paper›PMID 36344707›Full record

ArticleNature cancer2022

MACHETE identifies interferon-encompassing chromosome 9p21.3 deletions as mediators of immune evasion and metastasis.

Francisco M Barriga, Kaloyan M Tsanov, Yu-Jui Ho, Noor Sohail, Amy Zhang, Timour Baslan, Alexandra N Wuest, Isabella Del Priore, Brigita Meškauskaitė, Geulah Livshits and 10 more

Open access · hybridAbstract read
In one paragraph

Article in Nature cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed
8.8field-weighted citation impact, top 1% 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

90 citing papers in PubMed, 110 citations in OpenAlex.

  1. Trial
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  5. Comprehensive Genomic and Transcriptomic Characterization of MTAP Loss across Advanced Solid Tumors.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Observational
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  11. Genomics ofJCO precision oncology · 2026
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  15. Review
  16. Review
  17. Article
  18. Durvalumab Plus Chemotherapy in Patients WithJTO clinical and research reports · 2026
    Article
  19. Article
  20. Article

30 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 3 institutions in 2 countries.

Francisco M Barriga *Cancer Biology & Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID http://orcid.org/0000-0002-0996-7707
Kaloyan M Tsanov *Cancer Biology & Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Yu-Jui HoCancer Biology & Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Noor SohailProgram for Computational and Systems Biology, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Amy ZhangPanCuRx Translational Research Initiative, Ontario Institute for Cancer Research, Toronto, Ontario, Canada.
Timour BaslanCancer Biology & Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Alexandra N WuestCancer Biology & Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Isabella Del PrioreLouis V. Gerstner Jr. Graduate School of Biomedical Sciences, New York, NY, USA.
Brigita MeškauskaitėProgram for Computational and Systems Biology, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Geulah LivshitsCancer Biology & Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Direna Alonso-CurbeloCancer Biology & Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Janelle SimonCancer Biology & Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Almudena Chaves-PerezCancer Biology & Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Dafna Bar-SagiDepartment of Biochemistry, New York University School of Medicine, New York, NY, USA.
Christine A Iacobuzio-DonahueDavid M. Rubenstein Center for Pancreatic Cancer Research, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID http://orcid.org/0000-0002-4672-3023
Faiyaz NottaPanCuRx Translational Research Initiative, Ontario Institute for Cancer Research, Toronto, Ontario, Canada.
Ronan ChaligneProgram for Computational and Systems Biology, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID http://orcid.org/0000-0003-4332-3291
Roshan SharmaProgram for Computational and Systems Biology, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Dana Pe'erProgram for Computational and Systems Biology, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID http://orcid.org/0000-0002-9259-8817
Scott W LoweCancer Biology & Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA. lowes@mskcc.org.ORCID http://orcid.org/0000-0002-5284-9650
Memorial Sloan Kettering Cancer Center · USOntario Institute for Cancer Research · CANew York University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
VIRAL TRANSACTIVATIONP01CA013106 · NCI · COLD SPRING HARBOR LABORATORY · PI William Richard McCombie · 1985 to 2026
$116.8M
Translational Research in Oncology Training ProgramT32CA160001 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI SAWYERS, CHARLES L. · 2011 to 2020
$2.0M
Howard Hughes Medical InstituteNCI NIH HHS P01 CA013106NCI NIH HHS P30 CA008748NCI NIH HHS T32 CA160001
6 · The paper itself

Abstract

The most prominent homozygous deletions in cancer affect chromosome 9p21.3 and eliminate CDKN2A/B tumor suppressors, disabling a cell-intrinsic barrier to tumorigenesis. Half of 9p21.3 deletions, however, also encompass a type I interferon (IFN) gene cluster; the consequences of this co-deletion remain unexplored. To functionally dissect 9p21.3 and other large genomic deletions, we developed a flexible deletion engineering strategy, MACHETE (molecular alteration of chromosomes with engineered tandem elements). Applying MACHETE to a syngeneic mouse model of pancreatic cancer, we found that co-deletion of the IFN cluster promoted immune evasion, metastasis and immunotherapy resistance. Mechanistically, IFN co-deletion disrupted type I IFN signaling in the tumor microenvironment, leading to marked changes in infiltrating immune cells and escape from CD8

Indexed as

InterferonsNeoplasmsAnimalsChromosome DeletionChromosomesImmune EvasionMiceTandem Repeat SequencesTumor MicroenvironmentInterferons

Identifiers

PMID36344707
PMCPMC9701143
OpenAlexW4308458365

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.