Evidence map›Paper›PMID 42222275›Full record

ReviewExploration of targeted anti-tumor therapy2026

RNA therapeutic targeting of recalcitrant and rare cancers.

Afeez Adekunle Ishola, Nalini Devi Verusingam, Bashir Lawal

Abstract readReview
In one paragraph

Review in Exploration of targeted anti-tumor therapy, 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

3 authors.

Afeez Adekunle IsholaDevelopmental Therapeutics Branch (DTB), National Cancer Institute (NCI), National Institute of Health (NIH), Bethesda, MD 20892, USA.ORCID https://orcid.org/0000-0001-7047-922X
Nalini Devi VerusingamDepartment of Research and Development, National Cancer Council (MAKNA), Kuala Lumpur 50450, Malaysia.ORCID https://orcid.org/0000-0002-2232-0502
Bashir LawalUPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, PA 15260, USA.ORCID https://orcid.org/0000-0003-0676-5875

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In 2013, more than a decade ago, the "Recalcitrant Cancer Research Act of 2012" was signed into law in the USA. Recalcitrant cancers are among the leading causes of global cancer morbidity and mortality. At the inception of the act, priority was placed on lungs and pancreatic cancers. Despite the tremendous advancement achieved in the research and treatment of said 'recalcitrant cancers' in the form of developing novel or modified small molecule and antibody drugs, modest improvement has been recorded for patients' survival. Also, current mortality and morbidity for recalcitrant cancers keep increasing. Similarly, rare cancers only enjoy very meager research and drug development efforts globally. Consequently, very limited advancement has been made towards therapeutic development targeting rare cancers. Hence, the current situation calls for re-strategizing research efforts and exploring different treatment modalities towards combating recalcitrant and rare cancers. On this note, RNA therapeutics strategy holds a unique and vital prospect because of its propensity to target coding and non-coding RNA transcripts in the biological system. Moreover, RNA therapeutics such as lncRNAs and circRNAs have been established to even modulate protein expressions and biological phenotypic activity through RNA-protein interactions. Therefore, the current review aimed at summarizing existing literature, clinical trials, and elucidating the important prospect of RNA therapeutics in mitigating the recalcitrant and rare cancers menace.

Indexed as

DNA drugsnon-coding RNArare cancersrecalcitrant cancersRNA therapeutics

Identifiers

PMID42222275
PMCPMC13220128

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.