Evidence map›Paper›PMID 42220437›Full record

ReviewOncology research2026

CHK1 as a Metabolic and Immunological Regulator: Implications for Cancer Therapy.

Maria Franza, Aurora Melfi, Filippo Acconcia, Alessandra di Masi

Abstract readReview
In one paragraph

Review in Oncology research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Maria FranzaDepartment of Science, Roma Tre University, Rome, Italy.
Aurora MelfiDepartment of Science, Roma Tre University, Rome, Italy.
Filippo AcconciaDepartment of Science, Roma Tre University, Rome, Italy.
Alessandra di MasiDepartment of Science, Roma Tre University, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Checkpoint kinase 1 (CHK1), a key regulator of cell cycle checkpoints, plays a central role in the DNA damage response network, serving as a critical mediator that links DNA damage detection to DNA repair mechanisms. In recent years, several other cellular functions of CHK1 have gradually been discovered. As well as monitoring genomic integrity, CHK1 coordinates the timing of DNA replication with the availability of metabolic resources. This prevents unscheduled DNA synthesis from exceeding the cell's metabolic capacity and causing DNA damage. CHK1 activity also contributes to tumour immune surveillance and the modulation of immune cell infiltration and immune escape mechanisms within the tumour microenvironment. Furthermore, CHK1 is involved in the regulation of differentiation and epigenetics. This perspective on CHK1 provides a strategy foundation for next-generation combinatorial therapies. Indeed, the data presented herein underscores the potential of novel therapeutic strategies that target diverse aspects of tumour biology in a simultaneous manner. Despite the current lack of clinically approved CHK1 inhibitors, the pleiotropic roles of this kinase make it an attractive and promising target for new cancer therapies. The present review aims to analyze the structural and functional aspects of CHK1, with a particular focus on its "non-canonical" functions.

Indexed as

Checkpoint Kinase 1NeoplasmsAnimalsDNA DamageHumansMolecular Targeted TherapyTumor MicroenvironmentCheckpoint Kinase 1CHEK1 protein, humancancer therapycheckpoint inhibitionCheckpoint kinase 1 (CHK1)glycolysisimmune evasionimmunomodulationmetabolismsynthetic lethality

Identifiers

PMID42220437
PMCPMC13220075

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Registered trials

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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.