Evidence map›Paper›PMID 35115556›Full record

ArticleNature communications2022

Receptor-interacting protein kinase 2 (RIPK2) stabilizes c-Myc and is a therapeutic target in prostate cancer metastasis.

Yiwu Yan, Bo Zhou, Chen Qian, Alex Vasquez, Mohini Kamra, Avradip Chatterjee, Yeon-Joo Lee, Xiaopu Yuan, Leigh Ellis, Dolores Di Vizio and 9 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
6.2field-weighted citation impact, top 3% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
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  3. Article
  4. Hsa_circ_0030568 Promotes the Proliferation and Migration of Prostate Cancer CellsCombinatorial chemistry & high throughput screening · 2026
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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

19 authors at 3 institutions in 1 country.

Yiwu Yan *Department of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Bo Zhou *Department of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Chen QianDepartment of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Alex VasquezDepartment of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Mohini KamraDepartment of Chemistry and Purdue University Center for Cancer Research, Purdue University, West Lafayette, IN, USA.
Avradip ChatterjeeDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Yeon-Joo LeeDepartment of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0002-6605-8761
Xiaopu YuanDepartment of Pathology and Laboratory Medicine, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Leigh EllisDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0003-4739-5049
Dolores Di VizioDepartment of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Edwin M PosadasDepartment of Medicine, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Natasha KyprianouDepartment of Urology, Icahn School of Medicine at Mount Sinai, New York, New York, NY, USA.ORCID http://orcid.org/0000-0002-8713-3599
Beatrice S KnudsenDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0002-7589-7591
Kavita ShahDepartment of Chemistry and Purdue University Center for Cancer Research, Purdue University, West Lafayette, IN, USA.ORCID http://orcid.org/0000-0002-0451-1305
Ramachandran MuraliDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0002-8384-2793
Arkadiusz GertychDepartment of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0002-3107-602X
Sungyong YouDepartment of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0003-3513-1783
Michael R FreemanDepartment of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0001-8142-3432
Wei YangDepartment of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA. wei.yang@cshs.org.ORCID http://orcid.org/0000-0003-2575-3570
Cedars-Sinai Medical Center · USPurdue University West Lafayette · USIcahn School of Medicine at Mount Sinai · US

Funding

Racial Differences in Prostate Cancer Molecular SubtypingR01CA220327 · NCI · CEDARS-SINAI MEDICAL CENTER · PI Stephen Jay Freedland, Michael R. Freeman · 2018 to 2026
$3.1M
Treatment-Induced Phenotypic Reprogramming in Prostate CancerR01CA232574 · NCI · UNIVERSITY OF KENTUCKY · PI KYPRIANOU, NATASHA · 2019 to 2023
$2.2M
Mechanisms of Prostate Cancer MetastasisR01CA271750 · NCI · CEDARS-SINAI MEDICAL CENTER · PI FREEMAN, MICHAEL R., GARRAWAY, ISLA PEARL · 2021 to 2025
$2.2M
High-throughput palmitoyl-proteomics profiling of extracellular vesicles for identification of biomarkers for early detection of clinically significant prostate cancerR01CA218526 · NCI · CEDARS-SINAI MEDICAL CENTER · PI DI VIZIO, DOLORES, HURLEY, PAULA JILL · 2017 to 2021
$2.0M
NCI NIH HHS R01 CA218526NCI NIH HHS R01 CA220327NCI NIH HHS R01 CA232574NCI NIH HHS R01 CA271750
6 · The paper itself

Abstract

Despite progress in prostate cancer (PC) therapeutics, distant metastasis remains a major cause of morbidity and mortality from PC. Thus, there is growing recognition that preventing or delaying PC metastasis holds great potential for substantially improving patient outcomes. Here we show receptor-interacting protein kinase 2 (RIPK2) is a clinically actionable target for inhibiting PC metastasis. RIPK2 is amplified/gained in ~65% of lethal metastatic castration-resistant PC. Its overexpression is associated with disease progression and poor prognosis, and its genetic knockout substantially reduces PC metastasis. Multi-level proteomics analyses reveal that RIPK2 strongly regulates the stability and activity of c-Myc (a driver of metastasis), largely via binding to and activating mitogen-activated protein kinase kinase 7 (MKK7), which we identify as a direct c-Myc-S62 kinase. RIPK2 inhibition by preclinical and clinical drugs inactivates the noncanonical RIPK2/MKK7/c-Myc pathway and effectively impairs PC metastatic outgrowth. These results support targeting RIPK2 signaling to extend metastasis-free and overall survival.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsCell Line, TumorCell ProliferationGene Knockout TechniquesHEK293 CellsHumansImidazolesKaplan-Meier EstimateMaleMiceMice, SCIDNeoplasm MetastasisPC-3 CellsProstatic NeoplasmsProtein Kinase InhibitorsImidazolesMYC protein, humanponatinibProtein Kinase InhibitorsProto-Oncogene Proteins c-mycPyridazinesReceptor-Interacting Protein Serine-Threonine Kinase 2

Identifiers

PMID35115556
PMCPMC8813925
OpenAlexW4210750219

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.