Study defines a possible target for future treatments for a deadly form of the disease

Study defines a possible target for future treatments for a deadly form of the disease
Typical prostate cancer cells (left) and neuroendocrine prostate cancer cells. The neuroendocrine cells’ disorganized appearance reflects their more aggressive nature. Credit: UCLA Broad Stem Cell Research Center

Scientists at the UCLA Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research have discovered that a protein produced by a cancer gene leads to the development of a deadly, late-stage form of prostate cancer called neuroendocrine prostate cancer. The discovery could be a significant step toward a more effective treatment.

The findings, which were published in the journal Cancer Cell, are particularly important because neuroendocrine prostate cancer does not respond to standard treatments, and men who are diagnosed with the disease typically live for less than a year afterward. Up to one-quarter of those who die of prostate cancer have the neuroendocrine subtype.

"Identifying the cellular changes that happen in cancer cells is key to the development of drugs that inhibit those changes and thereby stop the progression of the disease," said Dr. Owen Witte, founding director of the UCLA Broad Stem Cell Research Center and the study's lead author. Witte also is a Howard Hughes Medical Institute investigator and a member of the President's Cancer Panel, which reports to President Barack Obama.

With patients' consent, the researchers obtained non-cancerous prostate basal cells—which contain prostate stem cells that can regenerate all other types of prostate cells—from men who underwent at the Ronald Reagan UCLA Medical Center. They then added a gene called MYCN to those cells. MYCN produces a protein called N-Myc, which is known to play a role in several types of aggressive cancer. In prostate cancer specifically, it seems to turn less aggressive into the that form the aggressive neuroendocrine prostate cancer tumors.

Next, the researchers transplanted the basal cells with the added MYCN genes into mice. Those cells with elevated N-Myc levels grew into neuroendocrine prostate cancer tumors, said Dr. John Lee, the study's first author and a clinical instructor in the Division of Hematology Oncology at the UCLA David Geffen School of Medicine.

Lee said that knowledge gave the scientists a potential new target for treating neuroendocrine prostate cancer, and they set out to begin work on a new way to attack the disease.

Collaborating with Kevan Shokat and Dr. Clay Gustafson of UC San Francisco, the team found that an experimental drug called CD532 reduced the size of the tumors in the mice by 80 percent.

CD532 had been developed earlier by Shokat and Gustafson for a type of childhood nervous system cancer in which N-Myc also plays a role. The drug had been shown in preclinical studies to have promise for treating that disease, but it had not previously been tested for neuroendocrine prostate cancer.

CD532 works by changing the structure of a protein called Aurora A kinase, which stabilizes N-Myc. In the new research, CD532 effectively destabilized N-Myc and, as a result, suppressed the ' growth.

Witte's research has long sought to explain how disease develops on a cellular level. His discovery that a specific type of kinase activity, called tyrosine kinase, can play a role in certain types of leukemia became the foundation for the creation of Gleevec, the first targeted therapy for .

"Kinase activity is known to be implicated in many types of cancers, including chronic myelogenous leukemia, which is no longer fatal for many people due to the success of Gleevec," said Witte, who also is a member of the UCLA Jonsson Comprehensive Cancer Center and a professor of microbiology, immunology and molecular genetics at the Geffen School. "I believe we can accomplish this same result for people with neuroendocrine prostate cancer."

Prostate cancer is the second leading cause of cancer death in American men, after lung cancer. It is often treatable, but the chance of survival drops drastically if the tumor becomes resistant to traditional therapies and metastasizes.

Lee said the researchers' next steps will be to identify other drugs that may be effective for treating neuroendocrine .

CD532 has only been used in preclinical tests and has not been tested in humans or approved by the U.S. Food and Drug Administration as safe and effective for use in humans.

Explore further

Study identifies potential therapeutic targets for metastatic prostate cancer

More information: N-Myc Drives Neuroendocrine Prostate Cancer Initiated from Human Prostate Epithelial Cells. DOI:
Journal information: Cancer Cell

Citation: Study defines a possible target for future treatments for a deadly form of the disease (2016, April 1) retrieved 2 July 2020 from
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