Evidence map›Paper›PMID 38700457›Full record

ArticleJournal of the American Chemical Society2024

RuBi-Ruxolitinib: A Photoreleasable Antitumor JAK Inhibitor.

Estefania Rafic, Cindy Ma, Bobby B Shih, Hannah Miller, Rafael Yuste, Teresa Palomero, Roberto Etchenique

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. 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

7 authors.

Estefania RaficDepartamento de Química Inorgánica, Analítica y Química Física, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, INQUIMAE, CONICET, Buenos Aires C1428EHA, Argentina.
Cindy MaInstitute for Cancer Genetics, Columbia University, New York, New York 10032, United States.
Bobby B ShihInstitute for Cancer Genetics, Columbia University, New York, New York 10032, United States.
Hannah MillerInstitute for Cancer Genetics, Columbia University, New York, New York 10032, United States.ORCID 0000-0003-1959-4104
Rafael YusteDepartment of Biological Sciences, Columbia University, New York, New York 10027, United States.
Teresa PalomeroInstitute for Cancer Genetics, Columbia University, New York, New York 10032, United States.
Roberto EtcheniqueDepartamento de Química Inorgánica, Analítica y Química Física, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, INQUIMAE, CONICET, Buenos Aires C1428EHA, Argentina.ORCID 0000-0002-5485-8710

Funding

Reexamining the Role of Dendrites in Neuronal FunctionRM1NS132981 · NINDS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Jayeeta Basu, RAFAEL YUSTE · 2023 to 2026
$10.3M
Effect of GABAergic inhibition of dendritic spines on synaptic pruning in the medial prefrontal cortex during adolescenceR01MH115900 · NIMH · SUNY DOWNSTATE MEDICAL CENTER · PI SMITH, SHERYL S · 2019 to 2023
$3.2M
Single-cell characterization of tumor and microenvironment co-evolution in Peripheral T-cell LymphomasU01CA243073 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PALOMERO, TERESA, RABADAN, RAUL · 2019 to 2023
$3.0M
Role and Mechanisms of VAV1 alterations in Peripheral T-cell LymphomasR01CA256341 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PALOMERO, TERESA · 2021 to 2025
$1.8M
Mechanisms of Neuronal Ensembles in Visual CortexR01EY035248 · NEI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI RAFAEL YUSTE · 2024 to 2026
$1.7M
Mechanism of Transformation in T-Cell Lymphomas: Identification of Therapeutic TargetsF31CA261153 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SHIH, BOBBY BEN · 2021 to 2023
$137k
NCI NIH HHS F31 CA261153NCI NIH HHS R01 CA256341NCI NIH HHS U01 CA243073NEI NIH HHS R01 EY035248NIMH NIH HHS R01 MH115900NINDS NIH HHS RM1 NS132981
6 · The paper itself

Abstract

We describe the synthesis and biological testing of ruthenium-bipyridine ruxolitinib (RuBiRuxo), a photoreleasable form of ruxolitinib, a JAK inhibitor used as an antitumoral agent in cutaneous T-cell lymphomas (CTCL). This novel caged compound is synthesized efficiently, is stable in aqueous solution at room temperature, and is photoreleased rapidly by visible light. Irradiation of RuBiRuxo reduces cell proliferation and induces apoptosis in a light- and time-dependent manner in a CTCL cell line. This effect is specific and is mediated by a decreased phosphorylation of STAT proteins. Our results demonstrate the potential of ruthenium-based photocompounds and light-based therapeutic approaches for the potential treatment of cutaneous lymphomas and other pathologies.

Indexed as

Antineoplastic AgentsApoptosisCell ProliferationNitrilesPyrazolesPyrimidinesCell Line, TumorHumansJanus Kinase InhibitorsJanus KinasesLightMolecular StructureRutheniumAntineoplastic AgentsJanus Kinase InhibitorsJanus KinasesNitrilesPyrazolesPyrimidinesRuthenium

Identifiers

PMID38700457
PMCPMC12147467

What OpenQuestion holds

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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.