Evidence map›Paper›PMID 41088176›Full record

ReviewCancer cell international2025

The multiplex crosstalk between non-coding RNAs, programmed cell death and related mechanisms: a dynamic duo in hematological malignancies.

Mehrdad Hashemi, Niloufar Salimian, Nafiseh Sharifi, Pezhman Shafiei Asheghabadi, Zahra Zarearandi, Fatemeh Abdi, Saranaz SeyedAli Akbar, Reza Mohajer Shirazi, Mehrdad Bagheri Pozve, Armin Nikdehqan and 10 more

Abstract readReview
In one paragraph

Review in Cancer cell international, 2025. 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

20 authors.

Mehrdad HashemiFarhikhtegan Medical Convergent Sciences Research Center, Farhikhtegan Hospital, Faculty of Medicine, TMs. C., Islamic Azad University, Tehran, Iran.
Niloufar SalimianFarhikhtegan Medical Convergent Sciences Research Center, Farhikhtegan Hospital, Faculty of Medicine, TMs. C., Islamic Azad University, Tehran, Iran.
Nafiseh SharifiFarhikhtegan Medical Convergent Sciences Research Center, Farhikhtegan Hospital, Faculty of Medicine, TMs. C., Islamic Azad University, Tehran, Iran.
Pezhman Shafiei AsheghabadiFarhikhtegan Medical Convergent Sciences Research Center, Farhikhtegan Hospital, Faculty of Medicine, TMs. C., Islamic Azad University, Tehran, Iran.
Zahra ZarearandiFarhikhtegan Medical Convergent Sciences Research Center, Farhikhtegan Hospital, Faculty of Medicine, TMs. C., Islamic Azad University, Tehran, Iran.
Fatemeh AbdiFarhikhtegan Medical Convergent Sciences Research Center, Farhikhtegan Hospital, Faculty of Medicine, TMs. C., Islamic Azad University, Tehran, Iran.
Saranaz SeyedAli AkbarFarhikhtegan Medical Convergent Sciences Research Center, Farhikhtegan Hospital, Faculty of Medicine, TMs. C., Islamic Azad University, Tehran, Iran.
Reza Mohajer ShiraziFarhikhtegan Medical Convergent Sciences Research Center, Farhikhtegan Hospital, Faculty of Medicine, TMs. C., Islamic Azad University, Tehran, Iran.
Mehrdad Bagheri PozveFarhikhtegan Medical Convergent Sciences Research Center, Farhikhtegan Hospital, Faculty of Medicine, TMs. C., Islamic Azad University, Tehran, Iran.
Armin NikdehqanFarhikhtegan Medical Convergent Sciences Research Center, Farhikhtegan Hospital, Faculty of Medicine, TMs. C., Islamic Azad University, Tehran, Iran.
Mehrandokht NekavandFarhikhtegan Medical Convergent Sciences Research Center, Farhikhtegan Hospital, Faculty of Medicine, TMs. C., Islamic Azad University, Tehran, Iran.
Zeinab Khazaei KoohparDepartment of Cell and Molecular Biology, To.C., Islamic Azad University, Tonekabon, Iran.
Russel J ReiterDepartment of Cell Systems and Anatomy, UT Health San Antonio, San Antonio, TX, 78229, USA.
Najma FarahaniFarhikhtegan Medical Convergent Sciences Research Center, Farhikhtegan Hospital, Faculty of Medicine, TMs. C., Islamic Azad University, Tehran, Iran.
Mobina ShariatzadehFaculty of Medicine, Shahed University, Tehran, Iran. mobina.shariatzadeh@gmail.com.
Mina AlimohammadiDepartment of Immunology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Payman RahimzadehSurgical Research Society (SRS), Students' Scientific Research Center, Tehran University of Medical Sciences, Tehran, Iran. P.rahimzadeh76@gmail.com.
Afshin TaheriazamFarhikhtegan Medical Convergent Sciences Research Center, Farhikhtegan Hospital, Faculty of Medicine, TMs. C., Islamic Azad University, Tehran, Iran. a.taheriazam@iautmu.ac.ir.
Maliheh EntezariFarhikhtegan Medical Convergent Sciences Research Center, Farhikhtegan Hospital, Faculty of Medicine, TMs. C., Islamic Azad University, Tehran, Iran. mentezari@iautmu.ac.ir.
Kiavash HushmandiDepartment of Epidemiology, University of Tehran, Tehran, Iran. Houshmandi.kia7@ut.ac.ir.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hematological malignancies, including leukemia, lymphoma, and multiple myeloma (MM), are cancers originating in the hematopoietic system, characterized by diverse pathogenesis and clinical features. Non-coding RNAs (ncRNAs) such as microRNAs (miRNAs) and long non-coding RNAs, play critical roles in regulating gene expression and influencing cell fate. Accumulating evidence indicates that ncRNAs are key modulators of programmed cell death (PCD) pathways, affecting tumor development, progression, and drug resistance in these malignancies. PCD, a precisely programmed and regulated cell death process, is vital for maintaining tissue homeostasis and preventing the proliferation of dangerous cells. NcRNAs are implicated in the primary mechanisms underlying the development of drug resistance. The evasion of PCD is a hallmark of cancer, and ncRNAs can significantly impact these pathways, with dysregulation observed across leukemia, lymphoma, and myeloma, influencing PCD pathways and clinical outcomes. Understanding the ncRNA-PCD interplay is crucial for developing novel therapeutic strategies and improving patient outcomes. This review explores the functions, regulatory mechanisms, and potential applications of ncRNAs in modulating PCD in hematological malignancies, particularly leukemias, providing insights for future anti-tumor therapies.

Indexed as

ApoptosisHematologic neoplasmsLeukemiasNon-coding RNAsProgrammed cell death

Identifiers

PMID41088176
PMCPMC12523004

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.