Ehrlich-Lettre Ascites, Strain E

Cat.No.: CSC-C9376L

Species: Mus musculus (Mouse)

Source: Ascites

Morphology: epithelial

Culture Properties: monolayer

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Cat.No.
CSC-C9376L
Description
Virus Susceptibility: polyomavirus
Histopathology: carcinoma
Note: Tested and found negative for ectromelia virus(mousepox)
Species
Mus musculus (Mouse)
Source
Ascites
Recommended Medium
90% NCTC 135 medium + 10% h.i. FBS
Culture Properties
monolayer
Morphology
epithelial
Disease
Mouse Mammary Gland Malignant Neoplasm
Quality Control
Tests for mycoplasma, bacteria and fungi were negative
Storage and Shipping
Frozen with 52.5% RPMI-1640, 40% FBS, 7.5% DMSO at about 4-5 x 10^6 cells/ampoule; ship in dry ice; store in liquid nitrogen
Synonyms
Ehrlich-Lettre ascites strain E; Ehrlich-Lettre; Ehrlich Lettre; E-La; EAT; EAT strain E; Ehrlich ascites; Ehrlich
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.

Ehrlich-Lettre Ascites, Strain E (E-La) is a classic murine tumor cell line derived from the ascitic form of an undifferentiated carcinoma first reported in Swiss albino mice. This line has been used extensively in basic cancer biology research and was derived from explant culture of in vivo passaged tumor tissue. E-La cells show an epithelial cell-like morphology under adherent culture conditions. Cytogenetically, the line is near-triploid with a modal chromosome number of about 44 (normal mouse diploid number = 40) and specific marker chromosomes, including the characteristic "A" chromosome.

For in vitro propagation, the cells require a basal medium rich in nutrients formulated for mammalian cells supplemented with serum and essential amino acids such as L-glutamine. Cultures were maintained at 37°C in humidified 5% carbon dioxide and usually sub-cultured with a standard protease solution at 70-80% confluence. The E-La strain continues to be a valuable tool for tumorigenesis studies, chemotherapeutic efficacy evaluation and modelling of peritoneal carcinomatosis because of its reliable growth characteristics and maintained malignant phenotype.

Tumor Induction Patterns in Mice Inoculated with Irradiated EAC Cells

Balakin et al. investigated the pattern of tumor induction in mice inoculated with Ehrlich ascites carcinoma (EAC) cells irradiated ex vivo with high doses of carbon ions (C) or X-rays.

As shown in Figure 1, mice inoculated with non-irradiated cells formed tumors by day 5. On the other hand, tumors appeared later in groups receiving irradiated cells in a dose-dependent fashion. The first tumors appeared on day 7 (5 Gy), day 11 (10 Gy) and day 21 (20 Gy) for C irradiation. Tumors were observed on day 11 (20 Gy), day 14 (30 Gy) and day 18 (40 Gy) after X-ray irradiation

At day 30 the tumor incidence in the C groups was 88% (5 Gy), 89% (10 Gy) and 35% (20 Gy), and no tumors were observed at 30 Gy (Fig. 1a). The incidences were 88%, 70%, 80% and 0% at 20, 30, 40 and 60 Gy, respectively, by X-ray irradiation (Fig. 1b). Tumor latency was significantly increased with dose, but the percentage of tumors induced within one month was not significantly different at lower doses for either type of radiation. This is consistent with previous studies on the proton irradiated cells, which indicate that the tumor cell death at early time points may promote the proliferation and differentiation of cancer stem cells (CSCs) in a radiation type-dependent manner.

Dynamics of the appearance of tumors in mice after inoculation of EAC cells irradiated with: (a) carbon ions in the dose range of 5-30 Gy; (b) X-rays at doses of 20-60 Gy.

Fig. 1. Dynamics of the appearance of tumors in mice after inoculation of EAC cells irradiated with: (a) carbon ions in the dose range of 5-30 Gy; (b) X-rays at doses of 20-60 Gy (Balakin V E, Belyakova T A, et al., 2023).

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