Evidence map›Paper›PMID 41898674›Full record

ArticleInternational journal of molecular sciences2026

Interleukin-2 and Tretinoin for Myeloproliferative Neoplasms and to Target Type 1 Calreticulin-Driven Neoplasms: Advancements in Immune Regenerative Medicine.

Dipnarine Maharaj, Wen Zhang, Kawaljit Kaur, Jacqueline Gouvea

Abstract readCase Reports
In one paragraph

Article in International journal of molecular sciences, 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.

Dipnarine MaharajThe Maharaj Institute of Immune Regenerative Medicine, Boynton Beach, FL 33437, USA.ORCID 0000-0001-9825-1905
Wen ZhangThe Maharaj Institute of Immune Regenerative Medicine, Boynton Beach, FL 33437, USA.
Kawaljit KaurImmuneLink, LLC, Riverside, CA 92508, USA.ORCID 0000-0003-1936-5985
Jacqueline GouveaThe Maharaj Institute of Immune Regenerative Medicine, Boynton Beach, FL 33437, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stem cells, also known as progenitor cells, can differentiate into specialized cells for specific tissues. Genetic mutations and epigenetic changes may cause normal stem cells to become cancer-initiating cells. Research indicates that cells acquiring a mutation for myeloproliferative neoplasm (MPN) are likely to be long-term hematopoietic stem cells (LT-HSCs) at the top of the hematopoietic hierarchy. Natural killer (NK) cells play a crucial role in combating cancer by targeting and eliminating cancer stem cells (CSCs) while promoting their maturation. NK cells do this through direct lysis of CSCs or by releasing cytokines like interferon-gamma (IFN-γ) and tumor necrosis factor-alpha (TNF-α), which inhibit tumor growth and metastasis by driving differentiation of CSCs. Interleukin-2 (IL-2) enhances the activity of CD4+ and CD8+ T cells and boosts NK cell cytotoxicity. This study highlights a case of MPN with a more clinically aggressive Type 1 calreticulin (

Indexed as

CalreticulinInterleukin-2Myeloproliferative DisordersTretinoinAnimalsHumansImmunotherapyKiller Cells, NaturalMutationNeoplastic Stem CellsRegenerative MedicineCalreticulinInterleukin-2Tretinoincalreticulin (CALR) mutationcancer stem cells (CSCs)cytokinesimmunotherapyinterleukin-2 (IL-2)natural killer (NK) cellspersonalizedprecisionstem cells (SCs)targeted therapytretinoin

Identifiers

PMID41898674
PMCPMC13027028

What OpenQuestion holds

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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.