Evidence map›Paper›PMID 41762434›Full record

ReviewStem cell reviews and reports2026

Molecular Pathophysiology of Ischemic Stroke and Mesenchymal Stem Cell Based Therapeutic Strategies for Neural Tissue Regeneration: A Pre-clinical and Clinical Perspective.

Aisha Ishaque, Rida-E-Maria Qazi, Asmat Salim, Tuba Shakil Malick, Zoha Asif

Abstract readReview
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In one paragraph

Review in Stem cell reviews and reports, 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

5 authors.

Aisha IshaqueCollege of Molecular Medicine, Ziauddin University, Karachi, 75600, Pakistan. aisha.ishaque@zu.edu.pk.ORCID 0000-0002-5031-0651
Rida-E-Maria QaziCenter for Regenerative Medicine and Stem Cell Research, Aga Khan University, Karachi, 74800, Pakistan.
Asmat SalimDr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, 75270, Pakistan.
Tuba Shakil MalickDow University of Health Sciences, Karachi, Pakistan.
Zoha AsifCollege of Molecular Medicine, Ziauddin University, Karachi, 75600, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ischemic stroke (IS), also referred to as cerebral ischemia, is a neurological condition accompanied by long term or permanent physical disability. Various molecular mechanisms such as inflammation, oxidative stress, blood brain barrier (BBB) disruption, energy depletion, mitochondrial dysfunction etc., contribute to its pathophysiology and trigger death of neural tissues. Currently, there are limited therapeutic options for its treatment. Although, thrombectomy or thrombolytic drugs are available, but only beneficial for the management of acute phase and do not address the neurodegenerative aspects. Mesenchymal stem cells (MSCs) are predominantly used for regenerative applications due to their self-renewal, immunomodulatory, and neuronal differentiation potential which make them a suitable candidate for neural tissue regeneration at both pre-clinical and clinical levels. MSC derived exosomes and extracellular vesicles (EVs) also provide cell-free therapeutic option that potentially reduce inflammation, restore BBB integrity, and facilitate neural regeneration. The current review summarizes the molecular mechanisms associated with IS pathophysiology and therapeutic mechanisms exhibited by MSCs and their derived products. Furthermore, the review also highlights the clinical trials registered so far to examine the efficacy of MSCs and their derived products to validate the findings and address challenges associated with preclinical studies. A number of clinical trials have reported improvements in motor functions and neurological scores, demonstrating MSC based therapy as safe and effective to treat IS complications. However, there is still a need to fully optimize protocols for MSC source, delivery route, dose, and timing of administration to maximize therapeutic efficacy and ensure safety in future clinical applications.

Indexed as

Brain IschemiaIschemic StrokeMesenchymal Stem CellsMesenchymal Stem Cell TransplantationNerve RegenerationAnimalsBlood-Brain BarrierHumansClinicalExosomesExtracellular VesiclesIschemic StrokeMesenchymal Stem CellMolecular PathophysiologyNeural RegenerationPre-Clinical

Identifiers

What OpenQuestion holds

Textmetadata
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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.