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

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,...
Cancers Originate from Somatic Mutations in a Single Cell02:21

Cancers Originate from Somatic Mutations in a Single Cell

Cancer arises from mutations in the critical genes that allow healthy cells to escape cell cycle regulation and acquire the ability to proliferate indefinitely. Though originating from a single mutation event in one of the originator cells, cancer progresses when the mutant cell lines continue to gain more and more mutations, and finally, become malignant. For example, chronic myelogenous leukemia (CML) develops initially as a non-lethal increase in white blood cells, which progressively...
Cancers Originate from Somatic Mutations in a Single Cell02:21

Cancers Originate from Somatic Mutations in a Single Cell

Cancer arises from mutations in the critical genes that allow healthy cells to escape cell cycle regulation and acquire the ability to proliferate indefinitely. Though originating from a single mutation event in one of the originator cells, cancer progresses when the mutant cell lines continue to gain more and more mutations, and finally, become malignant. For example, chronic myelogenous leukemia (CML) develops initially as a non-lethal increase in white blood cells, which progressively...

You might also read

Related Articles

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

Sort by
Same author

Comparative Finite Element Analysis of Denosumab and Bazedoxifene on Pedicle Screw Stability in Osteoporotic Spines.

JOR spine·2025
Same author

Hypoxia/HIF Signaling Negatively Regulates Bone Marrow Adiposity after Radiation Exposure.

bioRxiv : the preprint server for biology·2025
Same author

Protein Phosphatase 1 Regulatory Subunit 3C integrates cholesterol metabolism and isocitrate dehydrogenase in chondrocytes and neoplasia.

Proceedings of the National Academy of Sciences of the United States of America·2025
Same author

Enabling adenosine signaling to promote aged fracture healing.

NPJ Regenerative medicine·2025
Same author

Impact of Lumbar Degenerative Changes on Vertebral Bone Strength: A Finite Element Analysis.

Journal of orthopaedic research : official publication of the Orthopaedic Research Society·2025
Same author

Single cell analysis of Idh mutant growth plates identifies cell populations responsible for longitudinal bone growth and enchondroma formation.

Scientific reports·2024

Related Experiment Video

Updated: Jul 5, 2026

Analysis of Side Population in Solid Tumor Cell Lines
06:26

Analysis of Side Population in Solid Tumor Cell Lines

Published on: February 23, 2021

Side population cells in human cancers.

Colleen Wu1, Benjamin A Alman

  • 1Program in Developmental and Stem Cell Biology, Hospital for Sick Children, University of Toronto, Toronto Medical Discovery Tower, East Tower, 101 College Street, Toronto, Ont., Canada M5G 1L7.

Cancer Letters
|May 20, 2008
PubMed
Summary
This summary is machine-generated.

Cancer stem cells (CSCs) can be identified by their ability to extrude dyes, forming a side population (SP). These SP cells share key CSC characteristics, including tumor-initiating capacity and drug resistance.

More Related Videos

Effective Detection of Hoechst Side Population Cells by Flow Cytometry
06:31

Effective Detection of Hoechst Side Population Cells by Flow Cytometry

Published on: August 23, 2024

Harnessing the DNA Dye-triggered Side Population Phenotype to Detect and Purify Cancer Stem Cells from Biological Samples
09:57

Harnessing the DNA Dye-triggered Side Population Phenotype to Detect and Purify Cancer Stem Cells from Biological Samples

Published on: May 10, 2017

Related Experiment Videos

Last Updated: Jul 5, 2026

Analysis of Side Population in Solid Tumor Cell Lines
06:26

Analysis of Side Population in Solid Tumor Cell Lines

Published on: February 23, 2021

Effective Detection of Hoechst Side Population Cells by Flow Cytometry
06:31

Effective Detection of Hoechst Side Population Cells by Flow Cytometry

Published on: August 23, 2024

Harnessing the DNA Dye-triggered Side Population Phenotype to Detect and Purify Cancer Stem Cells from Biological Samples
09:57

Harnessing the DNA Dye-triggered Side Population Phenotype to Detect and Purify Cancer Stem Cells from Biological Samples

Published on: May 10, 2017

Area of Science:

  • Oncology
  • Stem Cell Biology
  • Biochemistry

Background:

  • Cancer stem cells (CSCs) are implicated in tumor growth and recurrence.
  • Prospectively identifying CSCs is challenging due to the lack of universal surface markers across all tumor types.
  • Alternative methods are needed to isolate and study CSCs in various cancers.

Purpose of the Study:

  • To explore dye extrusion as a method for identifying cancer stem cells (CSCs).
  • To characterize the side population (SP) of cells that extrude Hoechst 33342 dye.
  • To assess the stem-like properties of SP cells isolated from tumors.

Main Methods:

  • Utilized Hoechst 33342 dye exclusion assay to identify side population (SP) cells.
  • Analyzed SP cells for tumor-initiating capacity.
  • Examined gene expression profiles of SP cells for stem-like markers.
  • Assessed the chemosensitivity of SP cells.

Main Results:

  • Side population (SP) cells, defined by their ability to exclude Hoechst 33342 dye, were identified.
  • SP cells demonstrated enrichment for tumor-initiating capacity compared to non-SP cells.
  • SP cells exhibited expression of stem-like genes.
  • SP cells showed increased resistance to chemotherapeutic drugs.

Conclusions:

  • Dye extrusion, specifically Hoechst 33342 exclusion, is a viable method for identifying a unique population of cells with stem-like properties.
  • Side population (SP) cells possess key cancer stem cell (CSC) characteristics, including self-renewal and drug resistance.
  • This technique offers a valuable approach for CSC research when specific surface markers are unknown.