Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

RNA Editing02:23

RNA Editing

RNA editing is a post-transcriptional modification where a precursor mRNA (pre-mRNA) nucleotide sequence is changed by base insertion, deletion, or modification. The extent of RNA editing varies from a few hundred bases, in mitochondrial DNA of trypanosomes, to a just single base, in nuclear genes of mammals. Even a single base change in the pre-mRNA can convert a codon for one amino acid into the codon for another amino acid or a stop codon. This type of re-coding can significantly affect the...
Adaptive Mechanisms in Cancer Cells02:53

Adaptive Mechanisms in Cancer Cells

Cancer cells accumulate genetic changes at an abnormally rapid rate due to the defects in the DNA repair mechanisms. From an evolutionary perspective, such genetic instability is advantageous for cancer development. Mutant cell lines accumulate a series of beneficial mutations that contribute to their progression into cancer.
Some of the advantages that cancer cells have on normal cells include - enhanced ability to divide without terminally differentiating, induce new blood vessel formation,...
Cancer Stem Cells and Tumor Maintenance02:40

Cancer Stem Cells and Tumor Maintenance

Early diagnosis and treatment can often cure cancer. However, even with treatment, residual cells called cancer stem cells (CSC) might remain, often causing tumor recurrence. These cancer stem cells possess the potential for self-renewal and multi-lineage differentiation and are often responsible for the therapeutic resistance displayed in most cancers.
Cancer stem cells are thought to originate from tissue-specific normal stem cells or progenitor cells. The normal stem cells usually reside in...
Adaptive Mechanisms in Cancer Cells02:53

Adaptive Mechanisms in Cancer Cells

Cancer cells accumulate genetic changes at an abnormally rapid rate due to the defects in the DNA repair mechanisms. From an evolutionary perspective, such genetic instability is advantageous for cancer development. Mutant cell lines accumulate a series of beneficial mutations that contribute to their progression into cancer.
Some of the advantages that cancer cells have on normal cells include - enhanced ability to divide without terminally differentiating, induce new blood vessel formation,...
Cancer Stem Cells and Tumor Maintenance02:40

Cancer Stem Cells and Tumor Maintenance

Early diagnosis and treatment can often cure cancer. However, even with treatment, residual cells called cancer stem cells (CSC) might remain, often causing tumor recurrence. These cancer stem cells possess the potential for self-renewal and multi-lineage differentiation and are often responsible for the therapeutic resistance displayed in most cancers.
Cancer stem cells are thought to originate from tissue-specific normal stem cells or progenitor cells. The normal stem cells usually reside in...
Distinctive Features of Adult Stem Cells vs Cancer Stem Cells01:18

Distinctive Features of Adult Stem Cells vs Cancer Stem Cells

A stem cell is an unspecialized cell that can divide without limit as needed and can, under specific conditions, differentiate into specialized cells.
Adult stem cells
Adult stem cells are tissue-specific; hence, they divide to develop the tissue from which they originate. One type of adult stem cell is the epithelial stem cell, which gives rise to the keratinocytes in the multiple layers of epithelial cells in the epidermis of the skin. Adult bone marrow has three distinct types of stem cells:...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Dysregulation of the inside-out signaling pathway in CNS-infiltrated pediatric T-cell acute lymphoblastic leukemia.

Research square·2026
Same author

Quantitative assessment of CD79B depletion as a biomarker of accelerated B cell progenitor aging.

Stem cell research·2026
Same author

Uncovering a role for METTL13 in malignant transformation of human hematopoietic stem cells and in the progression of pediatric leukemia.

Cell death & disease·2026
Same author

Optimal conditions for quantification of IRF4 mRNA and protein as a correlative biomarker in clinical cancer studies.

Journal of translational medicine·2026
Same author

APOBEC3B enhances the efficacy of PARP inhibitors in elimination of ovarian cancer stem cell.

Scientific reports·2026
Same author

Widespread remodeling of the RNA editome underlies transcriptional and clinical heterogeneity in pediatric acute lymphoblastic leukemia.

bioRxiv : the preprint server for biology·2025

Related Experiment Video

Updated: Jul 13, 2026

Studying Pancreatic Cancer Stem Cell Characteristics for Developing New Treatment Strategies
07:29

Studying Pancreatic Cancer Stem Cell Characteristics for Developing New Treatment Strategies

Published on: June 20, 2015

RNA editing-dependent epitranscriptome diversity in cancer stem cells.

Qingfei Jiang1, Leslie A Crews1, Frida Holm1

  • 1Division of Regenerative Medicine, Department of Medicine, Moores Cancer Center and Sanford Consortium for Regenerative Medicine, University of California, San Diego, La Jolla, California 92093, USA.

Nature Reviews. Cancer
|April 19, 2017
PubMed
Summary

Cancer stem cells (CSCs) evolve through natural selection, influenced by epitranscriptomic changes. These RNA modifications drive tumor growth and drug resistance, offering new therapeutic targets.

More Related Videos

Discovery of Driver Genes in Colorectal HT29-derived Cancer Stem-Like Tumorspheres
06:52

Discovery of Driver Genes in Colorectal HT29-derived Cancer Stem-Like Tumorspheres

Published on: July 22, 2020

Dissociation of Human and Mouse Tumor Tissue Samples for Single-cell RNA Sequencing
05:58

Dissociation of Human and Mouse Tumor Tissue Samples for Single-cell RNA Sequencing

Published on: August 16, 2024

Related Experiment Videos

Last Updated: Jul 13, 2026

Studying Pancreatic Cancer Stem Cell Characteristics for Developing New Treatment Strategies
07:29

Studying Pancreatic Cancer Stem Cell Characteristics for Developing New Treatment Strategies

Published on: June 20, 2015

Discovery of Driver Genes in Colorectal HT29-derived Cancer Stem-Like Tumorspheres
06:52

Discovery of Driver Genes in Colorectal HT29-derived Cancer Stem-Like Tumorspheres

Published on: July 22, 2020

Dissociation of Human and Mouse Tumor Tissue Samples for Single-cell RNA Sequencing
05:58

Dissociation of Human and Mouse Tumor Tissue Samples for Single-cell RNA Sequencing

Published on: August 16, 2024

Area of Science:

  • Oncology
  • Molecular Biology
  • Epigenetics

Background:

  • Cancer stem cells (CSCs) possess self-renewal and dormancy capabilities, driving tumor regeneration and progression.
  • Tumor evolution, akin to natural selection, is influenced by genetic mutations, epigenetic changes, and potentially the epitranscriptome.
  • The epitranscriptome, involving RNA modifications and RNA-binding proteins, dynamically regulates gene expression and RNA function.

Purpose of the Study:

  • To review the role of RNA processing and epitranscriptomic alterations in cancer stem cell generation and maintenance.
  • To explore the mechanisms of RNA methylation, editing, and splicing in the context of CSCs.
  • To highlight the potential of epitranscriptomic events as biomarkers and therapeutic targets for cancer.

Main Methods:

  • Literature review focusing on malignant RNA processing in CSCs.
  • Discussion of RNA methylation, RNA editing, and RNA splicing mechanisms.
  • Analysis of the functional consequences of aberrant epitranscriptomic regulation in human cancers.

Main Results:

  • Epitranscriptomic deregulation contributes significantly to the generation and maintenance of cancer stem cells.
  • Aberrant RNA processing mechanisms, including methylation, editing, and splicing, are implicated in CSC biology.
  • Dysregulated epitranscriptomic events are linked to cancer progression and the development of drug resistance.

Conclusions:

  • Malignant RNA processing plays a critical role in cancer stem cell generation, maintenance, and drug resistance.
  • Epitranscriptomic alterations represent promising novel biomarkers for CSCs.
  • Targeting epitranscriptomic events offers a potential new therapeutic strategy for cancer treatment.