Human Mammary Epithelial Cells: HMEpC, adult
SIGMA/830-05A
Synonym: HMEpc cells
Product Type: Product-on-demand
Cell Applications
(A) HMEPC monolayer. HMEpC immunolabeled for e-cadherin (B and D, green) and for cytokeratin 18 (C and D, red). Nuclei are visualized with DAPI (D, blue).
(A) HMEPC monolayer. HMEpC immunolabeled for e-cadherin (B and D, green) and for cytokeratin 18 (C and D, red). Nuclei are visualized with DAPI (D, blue).
| biological source | human mammary glands (normal) |
| growth mode | Adherent |
| karyotype | 2n = 46 |
| manufacturer/tradename | Cell Applications, Inc |
| morphology | epithelial |
| packaging | pkg of 500,000 cells |
| Quality Level | 100  |
| relevant disease(s) | cancer |
| shipped in | liquid nitrogen |
| storage temp. | −196°C |
| technique(s) | cell culture | mammalian: suitable |
| Application: | antitumor properties, glycoprotein expression, breast cancer treatment approaches, DNA damage, cell differentiation, effects of growth factors |
| Cell Line Origin: | Mammary Gland |
| Components: | 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. |
| General description: | Lot specific orders are not able to be placed through the web. Contact your local sales rep for more details. 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. |
| Preparation Note: | • 5th passage, >500,000 cells in Cell Basal Medium containing 10% FBS & 10% DMSO • Can be cultured at least 16 doublings |
| Subculture Routine: | Please refer to the HMEpC Culture Protocol . |
| RIDADR | NONH for all modes of transport |
| WGK Germany | WGK 3 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Storage Temp. | −196°C |
| UNSPSC | 41106514 |