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Related Concept Videos

Mesenchymal Stem Cells01:19

Mesenchymal Stem Cells

Mesenchymal stem cells (MSCs) are adult stem cells that can differentiate into most connective tissue cell types, except for hematopoietic cells, depending upon the source of MSCs. For example, bone-marrow-derived MSCs (BM-MSCs) can differentiate into osteocytes, hepatocytes, and pancreatic and neuronal cells. MSCs can be isolated from various sources such as bone marrow, placenta, adipose tissue, teeth, and Wharton’s jelly, a gelatinous substance in the umbilical cord. The ease of their access...
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Cadherins in Tissue Organization

The cadherins are a superfamily of cell adhesion molecules comprising over 180 variants, with specific tissues expressing a particular combination of cadherin types. Cadherins generally exhibit homophilic binding; i.e., cadherins on one cell bind to cadherins of the same or closely related type on another cell. Thus, cells of the same type have a specific affinity to bind to each other and sort themselves into clusters to form tissues.
Cell Sorting During Development
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The Tumor Microenvironment02:17

The Tumor Microenvironment

Every normal cell or tissue is embedded in a complex local environment called stroma, consisting of different cell types, a basal membrane, and blood vessels. As normal cells mutate and develop into cancer cells, their local environment also changes to allow cancer progression. The tumor microenvironment (TME) consists of a complex cellular matrix of stromal cells and the developing tumor. The cross-talk between cancer cells and surrounding stromal cells is critical to disrupt normal tissue...
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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.
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Related Experiment Video

Updated: Jun 9, 2026

Mammosphere Formation Assay from Human Breast Cancer Tissues and Cell Lines
10:51

Mammosphere Formation Assay from Human Breast Cancer Tissues and Cell Lines

Published on: March 22, 2015

Mesenchymal stem cells promote mammosphere formation and decrease E-cadherin in normal and malignant breast cells.

Ann H Klopp1, Lara Lacerda, Anshul Gupta

  • 1Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.

Plos One
|September 3, 2010
PubMed
Summary
This summary is machine-generated.

Mesenchymal stem cells (MSC) enhance breast cancer stem cell mammosphere formation and promote tumor growth. MSCs also decrease E-cadherin, a marker linked to breast cancer progression and therapy resistance.

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Non-enzymatic, Serum-free Tissue Culture of Pre-invasive Breast Lesions for Spontaneous Generation of Mammospheres
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Last Updated: Jun 9, 2026

Mammosphere Formation Assay from Human Breast Cancer Tissues and Cell Lines
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Mammosphere Assay Reveals Api5-Induced Stemness in Non-Tumorigenic Breast Epithelial Cell Lines
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Non-enzymatic, Serum-free Tissue Culture of Pre-invasive Breast Lesions for Spontaneous Generation of Mammospheres
09:49

Non-enzymatic, Serum-free Tissue Culture of Pre-invasive Breast Lesions for Spontaneous Generation of Mammospheres

Published on: November 8, 2014

Area of Science:

  • Oncology
  • Stem Cell Biology
  • Biomedical Research

Background:

  • Normal and malignant breast tissues harbor rare, self-renewing stem cells or tumor-initiating cells (TIC).
  • These cells can be enriched through mammosphere culture in 3D.

Purpose of the Study:

  • To investigate if human bone-marrow derived mesenchymal stem cells (MSC) enhance mammosphere formation.
  • To determine the impact of MSCs on breast cancer stem cell properties and tumor development.

Main Methods:

  • Assessing mammosphere formation in response to MSCs and MSC-conditioned media.
  • Analyzing cell adhesion molecule expression (E-cadherin, N-cadherin).
  • Evaluating tumor development in vivo after co-injection with MSCs.

Main Results:

  • MSCs dose-dependently increased mammosphere formation in HMEC, MCF-7, and SUM149 cells.
  • MSC-conditioned media significantly boosted mammosphere formation (6.4-21 fold).
  • Co-injection with MSCs reduced tumor latency and increased tumor growth, with decreased E-cadherin expression.

Conclusions:

  • MSCs enhance primary mammosphere formation in normal and malignant breast cells.
  • MSCs decrease E-cadherin expression, a factor associated with breast cancer progression and treatment resistance.