Scientists make breasts in a dish to study lactation

Scientists are making mammary gland organoids with 3D milk ducts that could shed light on lactation and breast cancer development.

A microscope image of a fluorescent purple branching structure
This is an image of a rabbit mammary gland organoid. Organoids are made of stem cells pushed to become specific types of organ cells.
(Image credit: Rauner Lab/Tufts University, CC BY-ND)

All mammals have mammary glands that produce milk, a feature that has fascinated scientists for many years. Questions such as why mammary glands evolved in the first place, how they have adapted across different species and what unique evolutionary pressures shaped their development remain largely unanswered.

To investigate how various species have evolved unique solutions to biological challenges, my team at the Rauner Lab of Tufts University School of Medicine is recreating mammalian diversity in a dish through miniature versions of mammary glands — organoids. These models can shed light on the fundamental biological processes behind milk production, tissue regeneration and the early stages of breast cancer development.

Gat Rauner
Research Assistant Professor of Developmental, Molecular and Chemical Biology, Tufts University

Tissue-resident adult stem cells are the source of organ and tissue development, regeneration and maintenance. In many tissues they are also suspected as cancer cells-of-origin, both due to their long life-span as well as their self-renewal and regenerative capacities. As such, adult stem cells are a link that connects the closely related biology of development and tumorigenesis. It is becoming increasingly clear that stemness is a cell state, rather than a final cell identity. Cells shift their state as part of normal development and of oncogenic progression and invasion. The regulatory mechanisms that control shifts in cell state also control development and cancer and appear to involve all levels of regulation: from genetic, epigenetic and epi-transcriptomic to post-transcription, post-translation and classic cell signaling pathways. I am interested in understanding the regulatory mechanisms that control adult stem cells in the contexts of development and cancer, particularly in the earliest stages of tumorigenesis, when the developmental program deviates towards cell transformation.