Evidence map›Paper›PMID 37738974›Full record

ArticleCancer cell2023

ZNF683 marks a CD8

Erin M Parry, Camilla K Lemvigh, Stephanie Deng, Nathan Dangle, Neil Ruthen, Binyamin A Knisbacher, Julien Broséus, Sébastien Hergalant, Romain Guièze, Shuqiang Li and 25 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer cell, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
16.8field-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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 71 citations in OpenAlex.

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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

35 authors at 10 institutions in 4 countries.

Erin M ParryDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Harvard Medical School, Boston, MA 02115, USA; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Camilla K LemvighDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Department of Health Technology, Technical University of Denmark, 2800 Kongens Lyngby, Denmark.
Stephanie DengDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Nathan DangleDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Neil RuthenDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Binyamin A KnisbacherBroad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Julien BroséusInserm UMRS1256 Nutrition-Génétique et Exposition Aux Risques Environnementaux (N-GERE), Université de Lorraine, 54000 Nancy, France; Université de Lorraine, CHRU-Nancy, Service d'hématologie Biologique, Pôle Laboratoires, 54000 Nancy, France.
Sébastien HergalantInserm UMRS1256 Nutrition-Génétique et Exposition Aux Risques Environnementaux (N-GERE), Université de Lorraine, 54000 Nancy, France.
Romain GuièzeCHU Clermont-Ferrand, 63000 Clermont-Ferrand, France; EA 7453 (CHELTER), Université Clermont Auvergne, 63001 Clermont-Ferrand, France.
Shuqiang LiDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA; Translational Immunogenomics Lab, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Wandi ZhangDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Connor JohnsonBroad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Jaclyn M LongBroad Institute of MIT and Harvard, Cambridge, MA 02142, USA; Department of Immunology, Blavatnik Institute, Harvard Medical School, Boston, MA 02115, USA; Evergrande Center for Immunologic Diseases, Harvard Medical School and Brigham and Women's Hospital, Boston, MA 02115, USA; Division of Gastroenterology, Hepatology, and Nutrition, Boston Children's Hospital, Boston, MA 02115, USA.
Shanye YinDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Lillian WernerDepartment of Data Science, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Annabelle AnandappaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Noelia PurroyDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Satyen GohilDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Giacomo OliveiraDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Harvard Medical School, Boston, MA 02115, USA.
Pavan BachireddyDepartment of Hematopoietic Biology and Malignancy, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Sachet A ShuklaDepartment of Hematopoietic Biology and Malignancy, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Teddy HuangDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Translational Immunogenomics Lab, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Joseph D KhouryDepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, USA.
Beenu ThakralDepartment of Hematopathology, University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Michael DickinsonPeter MacCallum Cancer Centre, Royal Melbourne Hospital, Melbourne, VIC, Australia; Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, VIC, Australia.
Constantine TamAlfred Health, Melbourne, VIC, Australia; Monash University, Melbourne, VIC, Australia.
Kenneth J LivakDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Translational Immunogenomics Lab, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Gad GetzBroad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Donna NeubergDepartment of Data Science, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Pierre FeugierInserm UMRS1256 Nutrition-Génétique et Exposition Aux Risques Environnementaux (N-GERE), Université de Lorraine, 54000 Nancy, France; Université de Lorraine, CHRU Nancy, service d'hématologie clinique, Nancy, France.
Peter KharchenkoDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA 02215, USA.
William WierdaDepartment of Leukemia, University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Lars Rønn OlsenDepartment of Health Technology, Technical University of Denmark, 2800 Kongens Lyngby, Denmark.
Nitin JainDepartment of Leukemia, University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Catherine J WuDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Harvard Medical School, Boston, MA 02115, USA; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA. Electronic address: Catherine_wu@dfci.harvard.edu.
Dana-Farber Cancer Institute · USBroad Institute · USThe University of Texas MD Anderson Cancer Center · USInserm · FRHarvard University · USMonash Health · AUTechnical University of Denmark · DKThe Royal Melbourne Hospital · AUUniversité Clermont Auvergne · FRUniversity of Nebraska Medical Center · US

Funding

ProteomicsP01CA206978 · NCI · DANA-FARBER CANCER INST · PI WU, CATHERINE JU-YING · 2016 to 2025
$17.0M
Personal tumor neoantigens for immunity against chronic lymphocytic leukemiaR01CA155010 · NCI · DANA-FARBER CANCER INST · PI Catherine Ju-Ying Wu · 2011 to 2026
$9.6M
ITSC for Leukemia: Novel Molecular Strategies for NCTN: "Individualized" TherapieU10CA180861 · NCI · OHIO STATE UNIVERSITY · PI BLOOMFIELD, CLARA D, MARCUCCI, GUIDO · 2014 to 2018
$3.4M
Single cell investigation of co-evolution in cancer cells and host cell immune microenvironmentR50CA251956 · NCI · DANA-FARBER CANCER INST · PI Shuqiang Li · 2020 to 2026
$1.4M
Tracing the Evolution of Chronic Lymphocytic Leukemia to Richter's Syndrome: Defining TransformationK08CA270085 · NCI · DANA-FARBER CANCER INST · PI Erin M Parry · 2022 to 2026
$945k
NCI NIH HHS K08 CA270085NCI NIH HHS P01 CA206978NCI NIH HHS R01 CA155010NCI NIH HHS R50 CA251956NCI NIH HHS U10 CA180861
6 · The paper itself

Abstract

Unlike many other hematologic malignancies, Richter syndrome (RS), an aggressive B cell lymphoma originating from indolent chronic lymphocytic leukemia, is responsive to PD-1 blockade. To discover the determinants of response, we analyze single-cell transcriptome data generated from 17 bone marrow samples longitudinally collected from 6 patients with RS. Response is associated with intermediate exhausted CD8 effector/effector memory T cells marked by high expression of the transcription factor ZNF683, determined to be evolving from stem-like memory cells and divergent from terminally exhausted cells. This signature overlaps with that of tumor-infiltrating populations from anti-PD-1 responsive solid tumors. ZNF683 is found to directly target key T cell genes (TCF7, LMO2, CD69) and impact pathways of T cell cytotoxicity and activation. Analysis of pre-treatment peripheral blood from 10 independent patients with RS treated with anti-PD-1, as well as patients with solid tumors treated with anti-PD-1, supports an association of ZNF683

Indexed as

Leukemia, Lymphocytic, Chronic, B-CellLymphoma, Large B-Cell, DiffuseCD8-Positive T-LymphocytesGene Expression RegulationHumansImmunotherapycheckpoint blockadechronic lymphocytic leukemiaHobitimmunotherapyPD-1Richter transformationsingle-cell RNA sequencingt cellstoxZNF683

Identifiers

PMID37738974
PMCPMC10618915
OpenAlexW4386926153

What OpenQuestion holds

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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.