Massey researchers identified protein involved in milk production during pregnancy as potential target for novel breast cancer therapies
VCU Massey Cancer Center researchers have identified a protein involved in milk production that stimulates the growth and spread of breast cancer and could ultimately serve as a target for novel therapies to treat breast cancer.
Charles Clevenger, M.D., Ph.D., and a team of researchers discovered that the enzyme cyclophilin A (CypA) regulates the Jak2/Stat5 genetic pathway. This pathway is responsible for the natural maturation of mammary glands as well as the development of breast cancer cells.
“This research identifies cyclophilin A as a relevant target for therapeutic intervention in breast cancer. Because FDA-approved drugs are available to inhibit the action of CypA, translation of these findings to breast cancer patients should be rapid,” said Clevenger, interim associate director for basic research, member of the Cancer Cell Signaling research program and Carolyn Wingate Endowed Chair in Cancer Research at VCU Massey Cancer Center. “No study to date had previously examined the loss of CypA function during mammary development and the formation of cancer.”
By deleting the CypA enzyme in mouse models with ER-positive and ER-negative breast cancer, Clevenger and his team were able to inhibit the activation of the Stat5 pathway. This inhibition correlated to an increase in mammary tumor latency, which means they were able to slow or completely halt the growth of breast cancer cells.
The discovery of CypA’s contribution to the development of breast cancer was helped by previous observations of prolactin receptor (PRLr) signaling. Prolactin is the hormone that is primarily responsible for the production of milk during pregnancy, and earlier research by Clevenger has also linked it to the growth of breast tumors. By more closely analyzing the genetic pathways associated with PRLr signaling (including Jak2 and Stat5), CypA was revealed to be a major participant in the activation of those pathways.
“This study demonstrated many similarities to other loss-of-function mouse models of the PRL-PRLr-Jak2-Stat5 signaling pathway. However, what distinguishes the CypA-deprived mouse models from the other genetic deletion models was the mice’s ability to still successfully lactate and nurse their offspring, despite the loss of an enzyme critical to mammary gland development,” said Clevenger, who is also the chair of pathology at the VCU School of Medicine.
Clevenger believes the mice’s continued ability to lactate is related to the fact that there is a significant, but not complete, deactivation of the Jak2/Stat5 signaling pathways.
The research, published in Cancer Research, builds upon a decade of work performed in Clevenger’s labs at Massey and Northwestern University. He said he and his team will continue to conduct further studies in pre-clinical models.
Clevenger collaborated on this research with Sonja Volker and Shannon Hedrick of Massey and the VCU Department of Pathology, and Yvonne Feeney of Northwestern University.
This study was supported by the National Institutes of Health Grant R01 CA173305, the American Association for Cancer Research/Breast Cancer Research Foundation Research Grant 10-60-26-CLEV and, in part, by Massey’s NIH-NCI Cancer Center Support Grant P30 CA016059.
Services in support of the research were generated by Massey’s Flow Cytometry, Transgenic/Knock-out Mouse and Microscopy Shared Resources.
The full version of this manuscript is available at: http://cancerres.aacrjournals.org/content/78/14/3877.long