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830-05A

Human Mammary Epithelial Cells: HMEpC, adult

Sinónimos:

HMEpc cells

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NACRES:
NA.81
UNSPSC Code:
41106514
Biological source:
human mammary glands (normal)
Growth mode:
Adherent
Morphology:
epithelial
Relevant disease(s):
cancer
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biological source

human mammary glands (normal)

Quality Segment

packaging

pkg of 500,000 cells

manufacturer/tradename

Cell Applications, Inc

growth mode

Adherent

karyotype

2n = 46

morphology

epithelial

technique(s)

cell culture | mammalian: suitable

relevant disease(s)

cancer

shipped in

liquid nitrogen

storage temp.

−196°C

General description

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Mammary Epithelial Cells provide an excellent model system to study many aspects of epithelial function and disease, particularly those related to cancerogenesis.

HMEpC have been utilized in numerous research publications, for example to:
  • Investigate the role of exosomes secreted by cancer cells in formation of tumor permissive microenvironment through manipulation of normal mammary epithelium (Dutta, 2014)
  • Serve as control in a study investigating antitumor properties of cannabinoids (Ligresti, 2006) and stem cell microenvironment (Rostovit, 2008)
  • Determine that differential expression of glycoproteins allows to classify human breast cells into normal, benign, malignant, basal, and luminal groups (Yen, 2011, 2013; Timpe, 2013)
  • Identify ALDH isoform 5A1 as a potential target for treatment of human breast ductal carcinoma (Kaur, 2012); and determine that combination of an anti-EGFR anti-VEGFR treatment using ZD6474 with phototherapy (UV-B) is more effective in treating breast cancer than either treatment alone (Sarkar, 2013)
  • Demonstrate that although SIRT deacetylates p53, it does not play a role in cell survival following DNA damage (Solomon, 2006)
  • Demonstrate the important roles of tumor suppressor Maspin by showing that it promotes mammary epithelial differentiation via its interaction with IRF6 (Bailey, 2008); mediates effects of IFN-γ on vacuolar pH, cathepsin D processing and autophagy, protects extracellular matrix (ECM) from degradation in normal mammary epithelia, and that Maspin loss in metastatic cancer leads to unrestricted ECM degradation, contributing to metastasis (Khalkhali-Ellis, 2007, 2008); and show that loss of EcSOD expression also promotes invasiveness by disrupting ECM (Teoh-Fitzgerald, 2012, 2013)
  • Investigate the role of shortened telomeres in initiation of genomic instability, cytokinesis failure and polyploidy (Tusell, 2008; Soler, 2009; Pampalona, 2012); and elucidate the role of Myc in malignancy by studying its ability to transform primary epithelial cells (Thibodeaux, 2009)
  • Demonstrate, along with Human dermal Fibroblasts, that resveratrol inhibits mono-ubiquitination of histone H2B (Gao, 2011)

HMEpC, along with Human Prostate Epithelial Cells, have also been used in a study demonstrating that TGF-b1 induces Smad 1/5/8 and Smad 2/3 phosphorylation and BMP signaling results only in Smad 1/5/8 phosphorylation in these primary epithelial cells, while in cancer cells BMP also elicits Smad2/3 activation, contributing to cancerogenesis (Holtzhausen, 2013).

Characterization: the cells have a characteristic morphology consistent with an epithelial origin and are positive for epithelial cell marker cytokeratin 18.

Application

antitumor properties, glycoprotein expression, breast cancer treatment approaches, DNA damage, cell differentiation, effects of growth factors

Biochem/physiol Actions

Mammary Gland

Preparation Note

  • 5th passage, >500,000 cells in Cell Basal Medium containing 10% FBS & 10% DMSO
  • Can be cultured at least 16 doublings

Please refer to the HMEpC Culture Protocol.

Other Notes

Cell Basal Medium containing 10% FBS & 10% DMSO

Disclaimer

RESEARCH USE ONLY. This product is regulated in France when intended to be used for scientific purposes, including for import and export activities (Article L 1211-1 paragraph 2 of the Public Health Code). The purchaser (i.e. enduser) is required to obtain an import authorization from the France Ministry of Research referred in the Article L1245-5-1 II. of Public Health Code. By ordering this product, you are confirming that you have obtained the proper import authorization.

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Este artículo
502-05A504-05A
biological source

human mammary glands (normal)

biological source

human bronchi (normal surface epithelium)

biological source

human trachea (normal surface epithelium)

morphology

epithelial

morphology

epithelial

morphology

epithelial

growth mode

Adherent

growth mode

Adherent

growth mode

Adherent

relevant disease(s)

cancer

relevant disease(s)

asthma; autoimmune diseases; cardiovascular diseases

relevant disease(s)

cardiovascular diseases

technique(s)

cell culture | mammalian: suitable

technique(s)

cell culture | mammalian: suitable

technique(s)

cell culture | mammalian: suitable

karyotype

2n = 46

karyotype

2n = 46

karyotype

2n = 46


Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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Protocolos

Mammary Epithelial Cells and primary epithelial cells from other tissue at Cell Applications, your worldwide provider of human & animal cells, antibodies.


Karthic Chandran et al.
Oncotarget, 7(13), 15577-15599 (2015-12-02)
Inflammatory and invasive breast cancers are aggressive and require better understanding for the development of new treatments and more accurate prognosis. Here, we detected high expression of PPARα in human primary inflammatory (SUM149PT) and highly invasive (SUM1315MO2) breast cancer cells



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SKUGTIN
830-05A04061833005354

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