Evidence mapPaperPMID 40901187Full record

ReviewAnnals of medicine and surgery (2012)2025

Innovative strategies for mitochondrial dysfunction in myeloproliferative neoplasms a step toward precision medicine.

Shinto Bosco, Shreya Singh Beniwal, Samid Soeb Munshi, Daniela Castro Calderón, Yujin Jeong, Alyanna Cabe Cacas, Sandeep Kumar, Pedro Henrique Serra Carvalho Dos Santos, Saif Syed, Ayush Dwivedi and 1 more

Abstract readReview
In one paragraph

Review in Annals of medicine and surgery (2012), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Shinto BoscoDr. D. Y Patil Medical College, Hospital and Research Centre, Dr. D. Y Patil Vidyapeeth (Deemed to be University), Pimpri, Maharashtra, India.ORCID https://orcid.org/0009-0004-0420-3355
Shreya Singh BeniwalLady Hardinge Medical College, Connaught Place, New Delhi, India.
Samid Soeb MunshiB.J. Medical College Civil Hospital Asarwa, Ahmedabad, India.ORCID https://orcid.org/0009-0005-8464-6849
Daniela Castro CalderónUniversidad Peruana de Ciencias Aplicadas (UPC), Lima, Perú.ORCID https://orcid.org/0009-0008-0608-8062
Yujin JeongIcahn School of Medicine at Mount Sinai/Elmhurst, New York, New York.ORCID https://orcid.org/0000-0002-6634-5840
Alyanna Cabe CacasUniversity of Santo Tomas Faculty of Medicine and Surgery, Manila, Philippines.ORCID https://orcid.org/0009-0003-3206-3348
Sandeep KumarPt. B.D. Sharma PGIMS, Rohtak, India.
Pedro Henrique Serra Carvalho Dos SantosFaculdade de Ciências Médicas de Santos, Centro Universitário Lusíada (UNILUS), Santos, Brazil.ORCID https://orcid.org/0009-0009-9142-0433
Saif SyedRoyal College of Surgeons in Ireland, Dublin, Ireland.ORCID https://orcid.org/0000-0002-4419-2273
Ayush DwivediDanylo Halytsky Lviv National Medical University, Ukraine.ORCID https://orcid.org/0009-0005-1955-9116
Mahmoud EiniehUniversity of Debrecen, Debrecen, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myeloproliferative neoplasms (MPNs) are clonal disorders of hematopoietic stem cells characterized by aberrant proliferation of myeloid lineages, driven primarily by mutations in JAK2, CALR, and myeloproliferative leukemia, leading to constitutive activation of the JAK-STAT pathway. Emerging evidence highlights mitochondrial dysfunction as a key factor in MPN pathogenesis, contributing to increased reactive oxygen species production, mitochondrial DNA mutations, and dysregulated mitochondrial dynamics, which collectively promote clonal expansion and apoptosis resistance. Targeting mitochondrial pathways has gained attention as a therapeutic strategy, with approaches including mitochondria-targeted antioxidants, metabolic inhibitors, and modulation of mitophagy and mitochondrial fission/fusion dynamics. However, challenges such as drug delivery specificity, therapeutic resistance, and off-target effects remain significant. Recent advances in precision medicine, incorporating genomic, transcriptomic, and proteomic profiling, offer a more personalized approach to MPN treatment by tailoring interventions to individual mutation patterns. Additionally, novel therapeutic strategies, including gene editing technologies, RNA-based therapies, and nanoparticle-mediated drug delivery systems, hold promise for overcoming current treatment limitations. The integration of artificial intelligence in drug discovery and biomarker identification further enhances the potential for targeted therapies. Future research should focus on refining these strategies, developing reliable biomarkers for patient stratification, and exploring combination therapies that enhance treatment efficacy while minimizing adverse effects. By addressing mitochondrial dysfunction as an underlying driver of MPNs, these emerging approaches have the potential to improve disease management, extend patient survival, and enhance quality of life. Also, this new approach of precision medicine allows patient stratification and ensures that treatments are formed according to the individual disease biology of each patient, which results in overall better outcomes.

Indexed as

combination drug therapydrug delivery systemsmitochondrial DNAmitochondrial dysfunctionmyeloproliferative disorderssignal transduction

Identifiers

PMID40901187
PMCPMC12401363

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.