Blocking a single gene renders tumours less aggressive, Johns Hopkins researchers find.
Researchers at Johns Hopkins have identified a gene that, when repressed in tumour cells, halts cell growth and a range of processes needed for tumours to enlarge and spread to distant sites.
The researchers hope that this so-called “master regulator” gene may be the key to developing a new treatment for tumours resistant to current drugs.
“This master regulator is normally turned off in adult cells, but it is very active during embryonic development and in all highly aggressive tumours studied to date,” said Dr. Linda Resar, an associate professor of medicine, oncology and paediatrics, and affiliate in the Institute for Cell Engineering at the Johns Hopkins University School of Medicine. “Our work shows for the first time that switching this gene off in aggressive cancer cells dramatically changes their appearance and behaviour.”
A description of the experiments appears in the May 2 issue of the journal PLOS ONE.
Long term research
Dr. Resar has been investigating genes in the master regulator’s family, known as high mobility group or HMG genes, for two decades. In addition to their role in cancer, these genes are essential for giving stem cells their special powers, and that’s no coincidence, she said. “Many investigators consider cancer cells to be the evil twin of stem cells, because like stem cells, cancer cells must acquire special properties to enable the tumour to grow and metastasise or spread to different sites,” she explained.
In a previous study, she and her team devised techniques to block the HMGA1 gene in stem cells in order to study its role in those cells. In their prior work, they discovered that HMGA1 is essential for reprogramming adult cells, like blood or skin cells, into stem cells that share most, if not all, properties of embryonic stem cells.
In the newly reported study, the Resar team applied the same techniques to several strains of human breast cancer cells in the laboratory, including the so-called triple negative cells — those that lack hormone receptors or HER2 gene amplification. Triple-negative breast cancer cells tend to behave aggressively and do not respond to many of our most effective breast cancer therapies. The Resar team blocked HMGA1 expression in aggressive breast cancer cells and followed their appearance and growth patterns.
“The aggressive breast cancer cells grow rapidly and normally appear spindle-shaped or thin and elongated. Remarkably, within a few days of blocking HMGA1 expression, they appeared rounder and much more like normal breast cells growing in culture,” said Dr. Resar.
The team also found that the cells with suppressed HMGA1 grow very slowly and fail to migrate or invade new territory like their HMGA1-expressing cousins.
The team next implanted tumour cells into mice to see how the cells would behave. The tumours with HMGA1 grew and spread to other areas, such as the lungs, while those with blocked HMGA1 did not grow well in the breast tissue or spread to distant sites.
“From previous work, we know that HMGA1 turns on many different genes needed during very early development, but it’s normally turned off by the time we’re born,” said postdoctoral fellow Sandeep Shah, who led the study. “Flipping that master regulator back on seems to be necessary for a cancer to become highly aggressive, and now we’ve seen that flipping HMGA1 off again can reverse that aggressive behaviour.”
The next step, Dr. Resar says, is to try to develop a therapy based on that principle. The team is working with other researchers at Johns Hopkins to see whether HMGA1-blocking molecules could be delivered to tumours inside nanoparticles. Another possible approach, she says, would be to block not HMGA1 itself, but one of the pathways or processes that it affects.
Other authors of the report were Leslie Cope, Weijie Poh, Amy Belton, Sujayita Roy, C. Conover Talbot, Jr., Saraswati Sukumar, and David L. Huso, all of The Johns Hopkins University School of Medicine.
This study was funded by the National Cancer Institute, the Maryland Stem Cell Research Fund, and the Safeway Breast Cancer Foundation.