Washington D.C [USA], Mar. 17 (ANI): Patients suffering from cancer may soon face better therapy options as a team of researchers has come up with a new drug delivery method that produced strong results in treating cancers in animal models, including some hard-to-treat solid and liquid tumours.
The new method involves a class of pharmaceuticals known as antibody-drug conjugates (ADCs), which include some of the most promising next-generation antibody therapeutics for cancer. ADCs can deliver a cytotoxic payload in a way that is remarkably tumor-selective. So far, three ADCs have been approved by the U.S. Food and Drug Administration (FDA), but neither attaches the drug to a defined site on the antibody.
"We've been working on this technology for some time," lead author Christoph Rader said. "It's based on the rarely used natural amino acid selenocysteine, which we insert into our antibodies. We refer to these engineered antibodies as selenomabs."
Antibodies are large immune system proteins that recognize unique molecular markers on tumor cells called antigens. On their own, Rader noted, antibodies are usually not potent enough to eradicate cancer. However, their high specificity for antigens makes them ideal vehicles for drug delivery straight to tumor cells.
"We now show for the first time that selenomab-drug conjugates, which are ADCs that utilize the unique reactivity of selenocysteine for drug
attachment, are highly precise, stable and potent compositions and promise broad utility for cancer therapy," he continued.
Along with its potency, Rader noted, the ADC's stability is critical to its effectiveness. The researchers found that their new ADCs showed excellent stability in human blood in vitro and in circulating blood in animal models. Moreover, the new ADCs were highly effective against HER2 breast cancer, a particularly difficult cancer to treat, and against CD138 multiple myeloma. Importantly, the ADCs did not harm healthy cells and tissues.
"The selenomab-drug conjugate significantly inhibited the growth of an aggressive breast cancer," said first author Xiuling Li. "Four of the five mice tested were tumor-free at the end of the experiment, a full six weeks after their last treatment."
The study appears in the journal Cell Chemical Biology. (ANI)