Triple-negative breast cancer has poor survival rates. However, the results of a new study — in which researchers discovered a stem cell pathway that may promote the disease — may lead to new treatments.
Over recent months, Medical News Today have covered many studies related to breast cancer and how it can be treated.
Now, scientists at the Cleveland Clinic Lerner Research Institute in Ohio claim that they have identified a new stem cell pathway that promotes highly aggressive triple-negative breast cancer.
In the study — which is
However, the main problem when it comes to treating triple-negative breast cancer cells is that they do not have receptors that allow them to bind to estrogen and progesterone.
Because typical breast cancer therapies use these receptors to target cancer cells, the absence of these receptors help triple-negative breast cancer cells to evade treatment. As a result, triple-negative breast cancer is associated with low survival rates.
“Triple-negative breast cancer,” says study co-author Ofer Reizes, Ph.D., “is resistant to treatment and has a high recurrence rate.”
“This aggressive subtype accounts for about 15–20 percent of breast cancers,” he continues. “Our findings are at an early stage but we are hopeful that targeting these cancer stem cells will lead to new treatments to allow women to be treated successfully and improve their outcomes.”
Recently, we reported on research from the Case Comprehensive Cancer Center at Case Western Reserve University School of Medicine in Cleveland, OH, that suggested that an existing form of antimicrobial therapy may be effective against triple-negative breast cancer.
In that study, in vitro cancer cells treated with interferon-β had a significantly reduced likelihood of forming into tumors.
But Reizes and colleagues studied the protein connexin 26 (Cx26), which was previously believed to fight cancer cells but is now known to contribute to the progression of tumors.
By comparing healthy breast tissue with triple-negative breast cancer tissue, the researchers found that Cx26 is more active in the cancerous tissue. They also revealed that Cx26 is more prevalent in cancer stem cells than other stem cell types, and that Cx26 is linked to two other proteins also known to fuel tumor growth.
“Additional research is needed,” says co-author Justin Lathia, Ph.D., “but this discovery suggests that inhibiting Cx26 and the related pathway may be a promising new strategy for stopping or preventing triple-negative breast cancer stem cells from self-renewing and spreading.”
“It may also offer a target for diagnostic testing that helps clinicians predict health outcomes and relapse-free survival for patients with a specific cancer type.”
Justin Lathia, Ph.D.