Scientists Have Found A New Method Of Cancer Treatment.
Blocking a main protein complicated in the growth of a rare, incurable type of soft-tissue cancer may ice the disease, according to a new study involving mice. Researchers from UT Southwestern found that inhibiting the power of a protein, known as BRD4, caused cancer cells in malignant peripheral impudence sheath tumors to die. Malignant peripheral nerve sheath tumors are highly assertive soft-tissue cancers, or sarcomas, that form around nerves.
And "This study identifies a potential unfledged therapeutic target to combat malignant peripheral nerve sheath tumor, an incurable genre of cancer that is typically fatal," study senior author Dr Lu Le, an deputy professor of dermatology, said in a university news release. "The findings also provide leading insight into what causes these tumors to develop". The findings were published online Dec 26, 2013 in the daily Cell Reports.
Although malignant peripheral nerve sheath tumors can amplify randomly, about 50 percent of cases involve patients with a genetic disorder called neurofibromatosis category 1. This disorder affects one in 3500 people. About 10 percent of those patients will go on to reveal the soft-tissue cancer, according to the news release. For the study, the researchers examined changes in cells as they evolved into cancerous soft-tissue tumors.
They found that BRD4, which helps adjust gene activation, is produced at an abnormally record level in malignant peripheral nerve sheath tumor cancer cells. In turn, this causes another protein, known as BCL-2, to inhibit cancer cells from dying. When researchers reserved BRD4 in the mice, either genetically or with a drug called JQ1, the tumors got smaller.
So "These treatments suppressed tumor advancement and caused the cancer cells to withstand apoptosis, or cell death. This is why BRD4 inhibition is exquisitely useful against MPNSTs and may represent a paradigm shift in therapy for these patients," Le said. However, while studies involving animals can be useful, they commonly fail to produce similar results in humans.
Malignant perimetric nerve sheath tumors usually evolve from a noncancerous but often large and disfiguring tumor called a "plexiform neurofibroma". Traditionally, the remedying was to remove the tumor surgically. However, the release noted, this can be tough or impossible if the tumor is located near nerves. Patients can also undergo chemotherapy and radiation, but the effectiveness of these treatments is limited. The five-year survival count for these patients is about 50 percent, according to the info release rxlist. Right now, the class of drug used in the experiments is being evaluated in phase 1 and shape 2 trials for treatment of leukemia and a type of lung cancer.
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