Evidence map›Paper›PMID 42649906›Full record

ReviewCancers2026

Calcium-Orchestrated Vascular Collapse in Cancer Therapy: Mechanisms, Nanotherapeutic Platforms, and Translational Perspectives.

Fatima Zahra Kamal, Radu Lefter, Vasile Burlui, Alin Stelian Ciobîcă, Gabrielle Dăscălescu, Said Rammali, Andrei Luca, Ancuța Andreea Miler, Hina Alim, Otilia Novac and 2 more

Abstract readReview
In one paragraph

Review in Cancers, 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

12 authors.

Fatima Zahra KamalCare and Health Biology Team, 2S2D Laboratory, Higher Institute of Nursing Professions and Health Technical (ISPITS), Casablanca 20250, Morocco.ORCID 0000-0001-5748-8500
Radu LefterCenter of Biomedical Research, Romanian Academy, 700506 Iasi, Romania.
Vasile BurluiDepartment of Biology, Faculty of Biology, Alexandru Ioan Cuza University of Iasi, 700505 Iasi, Romania.
Alin Stelian CiobîcăDepartment of Biology, Faculty of Biology, Alexandru Ioan Cuza University of Iasi, 700505 Iasi, Romania.
Gabrielle DăscălescuDepartment of Biology, Faculty of Biology, Alexandru Ioan Cuza University of Iasi, 700505 Iasi, Romania.ORCID 0009-0001-1962-7861
Said RammaliLaboratory of Agro-Alimentary and Health, Faculty of Sciences and Techniques, Hassan First University of Settat, Settat 26000, Morocco.
Andrei LucaFaculty of Medicine, Carol Davila University of Medicine and Pharmacy, 020022 Bucharest, Romania.
Ancuța Andreea MilerFaculty of Medicine, Grigore T. Popa University of Medicine and Pharmacy, 700115 Iasi, Romania.
Hina AlimDepartment of Life Sciences, University of Mumbai, Mumbai 400098, India.
Otilia NovacFaculty of Medicine, Grigore T. Popa University of Medicine and Pharmacy, 700115 Iasi, Romania.
Bouchaib BencharkiLaboratory of Agro-Alimentary and Health, Faculty of Sciences and Techniques, Hassan First University of Settat, Settat 26000, Morocco.
Bogdan NovacFaculty of Medicine, Grigore T. Popa University of Medicine and Pharmacy, 700115 Iasi, Romania.ORCID 0000-0003-4501-1718

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer therapy is increasingly focused on manipulating the tumor microenvironment rather than directly eradicating malignant cells. Vascular-targeting strategies are emerging, and calcium-mediated vascular disruption is an exciting approach through which rapid and irreversible blood flow shutdown can be achieved. Here, we overview the molecular and physiological basis of calcium signaling in vascular homeostasis and outline how unregulated calcium dysfunctions in endothelial cells compromise their functionality and represent therapeutic opportunities. Elevation of intracellular calcium concentrations in endothelial cells promotes their dysfunction, coagulation, mitochondrial collapse, oxidative stress, and ultimately apoptosis, resulting in catastrophic vascular depletion and secondary necrosis that follows such collapse. A promising area of calcium-mediated attack is the emergence of exciting nanotechnologies that result in the development of calcium phosphate, calcium carbonate, and calcium peroxide nanoparticles, exploiting the enhanced permeability and retention effect of nanoparticle therapeutics to achieve selective tumor accumulation and controlled calcium release. Indeed, hybrid therapeutic platforms that couple calcium dysregulation with chemotherapy, photodynamic therapy, sonodynamic therapy, immunotherapy, or thermal ablation can exhibit pronounced antitumor effects through synergistic means. There is good preclinical evidence for the feasibility of vascular collapse mediated via calcium dysregulation. The transition of calcium to the clinic faces hurdles in relation to biosafety, how to achieve precise delivery, pharmacokinetics, and regulatory harmonization. Compared to traditional vascular disrupting agents and anti-angiogenic therapies, calcium modalities can provide rapid occlusion of vessels, are less prone to resistance development, and potentially have less systemic toxicity. Overall, calcium-mediated vascular collapse is thus an exciting next-generation technology for the vascular-targeted treatment of cancer, and likely to play an important role in precision oncology therapeutics.

Indexed as

calcium signalingendothelial dysfunctionnanomedicinetargeted drug deliverytumor microenvironmenttumor vasculature

Identifiers

PMID42649906
PMCPMC13511603

What Socratic holds

Textmetadata
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 Socratic graph.