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A Human Organoid System That Self-organizes to Recapitulate Growth and Differentiation of a Benign Mammary Tumor

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Specialty Science
Date 2019 May 19
PMID 31101720
Citations 11
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Abstract

As 3D culture has become central to investigation of tissue biology, mammary epithelial organoids have emerged as powerful tools for investigation of epithelial cell polarization and carcinogenesis. However, most current protocols start from single cells suspended in Matrigel, which can also restrict cell differentiation and behavior. Here, we show that the noncancerous mammary cell line HMT-3522 S1, when allowed to spontaneously form cell aggregates ("spheroids") in medium without Matrigel, switches to a collective growth mode that recapitulates many attributes of "usual ductal hyperplasia" (UDH), a common benign mammary lesion. Interestingly, these spheroids undergo a complex maturation process reminiscent of embryonic development: solid-cell cords form their own basement membrane, grow on the surface of initially homogeneous cell aggregates, and form asymmetric lumina lined by two distinct cell types that express basal and luminal cytokeratins. This sequence of events provides a cellular mechanism that explains how the characteristic crescent-shaped, asymmetrical lumina form in UDH. Our results suggest that HMT-3522 S1 spheroids are useful as an in vitro model system to study UDH biology, glandular lumen formation, and stem cell biology of the mammary gland.

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References
1.
Hebner C, Weaver V, Debnath J . Modeling morphogenesis and oncogenesis in three-dimensional breast epithelial cultures. Annu Rev Pathol. 2007; 3:313-39. DOI: 10.1146/annurev.pathmechdis.3.121806.151526. View

2.
Ohuchi N, Abe R, Takahashi T, Tezuka F, KYOGOKU M . Three-dimensional atypical structure in intraductal carcinoma differentiating from papilloma and papillomatosis of the breast. Breast Cancer Res Treat. 1985; 5(1):57-65. DOI: 10.1007/BF01807651. View

3.
Boras-Granic K, Dann P, Wysolmerski J . Embryonic cells contribute directly to the quiescent stem cell population in the adult mouse mammary gland. Breast Cancer Res. 2014; 16(6):487. PMC: 4308878. DOI: 10.1186/s13058-014-0487-6. View

4.
Ikenouchi J, Umeda K, Tsukita S, Furuse M, Tsukita S . Requirement of ZO-1 for the formation of belt-like adherens junctions during epithelial cell polarization. J Cell Biol. 2007; 176(6):779-86. PMC: 2064052. DOI: 10.1083/jcb.200612080. View

5.
Freyer J . Role of necrosis in regulating the growth saturation of multicellular spheroids. Cancer Res. 1988; 48(9):2432-9. View