Evidence map›Paper›PMID 41479113›Full record

ReviewExperientia supplementum (2012)2026

The Potential of Noncoding RNAs-siRNAs in Cancer Research and Therapy: Challenges and Solutions.

Himanshu, Mudasir Bashir, Moien Lone, Mohsin Maqbool

Abstract readReview
PubMed Publisher
In one paragraph

Review in Experientia supplementum (2012), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
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.

HimanshuDepartment of Pathology, All India Institute of Medical Sciences (AIIMS), New Delhi, India.
Mudasir Bashir *Department of Physiology, Graphic Era Institute of Medical Sciences (GEIMS), Dehradun, Uttarakhand, India.
Moien Lone *Department of Pathology and Laboratory Medicine, University of California, Los Angeles, CA, USA.
Mohsin MaqboolDepartment of Cancer Biology, Jefferson University, Philadelphia, PA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Noncoding RNAs (ncRNAs) are RNA molecules, which play critical roles in regulating gene expression and cellular activities, influencing processes like differentiation, proliferation, and cell survival, unlike messenger RNAs (mRNAs) that act as templates for protein production. Examples of ncRNAs include small interfering RNAs (siRNAs), microRNAs (miRNAs), ribosomal RNAs, transfer RNAs, small nucleolar RNAs (sno RNAs), and small nuclear RNAs (snRNAs). Small interfering RNAs (siRNAs) are a type of noncoding RNA that function primarily by silencing specific genes through a process called RNA interference (RNAi), in which they bind to complementary messenger RNA (mRNA) molecules, causing their degradation and preventing the translation of that mRNA into protein; essentially, they act as a "gene silencing" mechanism by targeting and destroying specific transcripts. In this chapter, we review the biogenesis, functions, and role of RNAs (siRNAs), in cancer research and role in therapy. siRNA (small interfering RNA) denotes small interfering RNA, consisting of 21-25 nucleotides. Discovery of siRNA (small interfering RNA) has been a significant breakthrough in biology. Small interfering RNAs (siRNAs) are single-stranded RNAs that are formed by the cleavage of longer double-stranded RNAs by the enzyme DICER1 within the RISC loading complex, which includes DICER1, an Argonaute protein, and either TARBP2 or PRKRA (PACT). Small interfering RNA (siRNA) is essential for health as it serves as a natural gene silencing tool, controlling gene expression posttranscriptionally, and is involved in several cellular processes such as development, immune response, and stress response; however, when not regulated properly, siRNAs may lead to diseases like cancer and viral infections, positioning them as a promising therapeutic target for targeted gene silencing therapies. siRNAs play a pivotal role in RNA interference (RNAi), a natural cellular process where they degrade complementary mRNA targets, preventing protein synthesis. This gene silencing mechanism has proven to be a valuable tool for controlling gene expression in research and therapeutic contexts. In cancer, siRNAs offer a promising approach to selectively silence oncogenes or other genes involved in tumor progression, thus hindering the development and spread of malignancies. However, the therapeutic potential of siRNAs faces several challenges, including efficient delivery to target cells, off-target effects, and stability issues. This chapter focuses on the biogenesis and functional significance of siRNAs, exploring their roles in cancer research and their promising therapeutic potential. With the continued advancement of RNA-based technologies, siRNAs hold considerable promise as a powerful tool for cancer treatment, offering new avenues for targeted therapies and personalized medicine.

Indexed as

Genetic TherapyNeoplasmsRNA, Small InterferingRNA, UntranslatedAnimalsGene Expression Regulation, NeoplasticHumansRNA InterferenceRNA, Small InterferingRNA, UntranslatedCancer researchGene expressionGene silencingMolecular therapyNoncoding RNAsOncogenesRNAiRNA interferencesiRNAsSmall interfering RNAs

Identifiers

What Socratic holds

Textmetadata
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.