image: The left image shows green fluorescent protein (GFP)-expressing cancer cells (green) and a normal lipid-filled adipocyte (red) at the surface of a control-treated tumor. The right image shows GFP-expressing cancer cells (green) and GFP-expressing cancer cells that have converted into adipocytes (green + red = dark yellow) upon trans-differentiation therapy. view more
Credit: Department of Biomedicine, University of Basel.
As cancer cells respond to cues in their microenvironment, they can enter a highly plastic state in which they are susceptible to transdifferentiation into a different type of cell. Researchers at the University of Basel in Switzerland exploited this critical phase, known as an epithelial-mesenchymal transition (EMT), to coax breast cancer cells in mice to turn into harmless fat cells. The proof-of-concept study appears January 14 in the journal Cancer Cell.
"The breast cancer cells that underwent an EMT not only differentiated into fat cells, but also completely stopped proliferating," says first author Gerhard Christofori, professor of biochemistry at the University of Basel. What's more, the primary tumor did not metastasize. "As far as we can tell from long-term culture experiments, the cancer cells-turned-fat cells remain fat cells and do not revert back to breast cancer cells," he says.
Epithelial cells undergoing EMT regress from terminally differentiated cells to a more immature state reminiscent of stem cells. EMT is essential for embryonic development, during which stem cells differentiate into a variety of cell types throughout the body, and for tissue regeneration such as wound healing. EMT and the inverse process, mesenchymal-epithelial transition (MET), are implicated in cancer's ability to metastasize.
Cells undergoing EMT or MET, Christofori says, are in a highly changeable state, providing a window of opportunity for therapeutic targeting, which the researchers tested in mouse models for metastatic breast cancer created by transplanting human breast cancer cells into the mammary fat pad of female mice.
When these mice received doses of two FDA-approved drugs--a cancer inhibitor and an anti-diabetic drug--their invasive cancer cells changed into fat cells. The drugs also suppressed the growth of primary tumors in the mice and prevented the tumors from metastasizing throughout the animals' bodies.
In particular, the researchers targeted a handful of aggressive cancer cells that had left the primary tumor and invaded surrounding tissue. These cells, which most likely had undergone an EMT, were readily converted to fat cells, while the remaining cancer cells within the tumor were no longer able to proliferate unchecked.
The researchers hypothesize that forcing a critical mass of cancerous cells to differentiate into fat cells could deplete a tumor's ability to fight off conventional chemotherapy. Next steps involve testing the EMT-targeted differentiation approach in combination with existing chemotherapies and in other types of cancers.
###
This work was supported by the Botnar Foundation Basel, the SystemsX.ch RTD project Cellplasticity, the SystemsX.ch MTD project MetastasiX, the Swiss National Science Foundation and the Swiss Cancer League.
Cancer Cell, Ronen et al.: "Gain Fat--Lose Metastasis: Converting Invasive Breast Cancer Cells into Adipocytes Inhibits Cancer Metastasis" https://www.cell.com/cancer-cell/fulltext/S1535-6108(18)30573-7
Cancer Cell (@Cancer_Cell), published by Cell Press, is a monthly journal that provides a high-profile forum to promote major advances in cancer research and oncology. The journal covers topics related to molecular and cellular mechanisms of cancer, mechanisms for the sensitivity and the resistance to cancer therapies, development of better cancer therapies, and clinical investigations. Visit: http://www.cell.com/cancer-cell. To receive Cell Press media alerts, contact press@cell.com.
Journal
Cancer Cell