Cancer Cells' DNA Repair Disrupted to Increase Radiation Sensitivity
Thursday, December 01, 2011
Shortening end caps on chromosomes in human cervical cancer cells disrupts DNA repair signaling, increases the cells’ sensitivity to radiation treatment and kills them more quickly, according to a study in Cancer Prevention Research.
Researchers would to like see their laboratory findings – published in the journal’s Dec. 5 print edition – lead to safer, more effective combination therapies for hard-to-treat pediatric brain cancers like medulloblastoma and high-grade gliomas. To this end, they are starting laboratory tests on brain cancer cells.
“Children with pediatric brain cancers don’t have very many options because progress to find new treatments has been limited the last 30 years,” said Rachid Drissi, PhD, principal investigator on the study and a researcher in the Division of Oncology at Cincinnati Children’s. “The ability to make cancer cells more sensitive to radiation could allow physicians to use lower radiation doses to lessen side effects. Too many children with brain cancer can develop disabilities or die from treatment.”
Before treating cells with ionizing radiation, the researchers blocked an enzyme called telomerase, found in over 90 percent of cancer cells but barely detectable in most normal human cells. In cancer cells, telomerase helps maintain the length of caps on the ends of chromosomes called telomeres. This helps cancer cells replicate indefinitely, grow and spread, Drissi said.
Unraveling DNA stability
Found on chromosomes in both cancerous and normal cells, telomeres are analogous to plastic caps that keep shoestring ends from unraveling. Telomeres help preserve DNA stability in cells by containing genetic miscues. This helps explain why cells with maintained or long telomeres appear to be more resistant to radiation.
In normal cells lacking the telomerase enzyme, telomeres get shorter each time cells divide. They continue doing so until normal cells stop dividing, reaching a condition called senescence. If this first cell-cycle “stop sign” is bypassed, cells continue dividing until telomeres become critically short and reach a second stopping point, when most cells die. In rare instances, cells bypass this second “stop sign” and survive. This survival is often associated with telomerase activation and the onset of cancer.
This was the basis for experiments Drissi and his colleagues conducted to compare the radiation sensitivity and survivability of cells based on telomere length. They also monitored DNA repair responses in the cells by looking for specific biochemical signs that indicate whether the repair systems are working.
The tests involved normal human foreskin cells – called fibroblasts – and human cervical carcinoma cells. They exposed the cells to ionizing radiation and analyzed DNA repair responses as telomeres became progressively shorter. In the cervical cancer cells, researchers blocked the telomerase enzyme before radiation treatment to induce progressively shorter telomeres.
Both late-stage noncancerous cells with shorter telomeres, and cancer cells with induced shorter telomeres, were more radiosensitive and died more quickly, according to the study.
Among cancer cells with maintained telomere length, close to 10 percent receiving the maximum dose of ionizing radiation used in the study (8 Gy, or Gray Units) survived the treatment. None of the cancer cells with the shortest telomeres survived that exposure.
Researchers said the cancer cells became more radiosensitive because material inside the chromosomes – called chromatin – compacted as telomeres became shorter. Compacted chromatin then disrupted the biochemical signaling of a protein called ATM (ataxia telangiectasia mutated).
ATM is a master regulator of DNA repair and cell division. It sends signals to activate other biochemical targets (H2AX, SMC1, NBS1 and p53) that help direct DNA repair and preserve genetic stability. In telomere-shortened cancer cells, the compacted chromatin inhibited ATM signaling to all of the chromatin-bound targets tested in the study. This disrupted DNA repair responses and increased radiation sensitivity.
Testing brain cancer cells
The researchers are now testing their findings in cells from hard-to-treat pediatric brain tumors. These tests begin as Drissi’s laboratory also leads correlative cancer biology studies of tumor samples from a current clinical trial. The trial is evaluating telomere shortening as a stand-alone therapy for pediatric cancer.
Managed through the National Institutes of Health’s Children’s Oncology Group (COG), the multi-institutional Phase 1 trial is testing the safety and tumor response capabilities of the drug Imetelstat, which blocks telomerase in cancer cells. Drissi serves on the clinical trial committee along with Maryam Fouladi, MD, MSc, and medical director of Neuro-Oncology at Cincinnati Children’s. She leads the medical center’s clinical participation in the trial.
Drissi and Fouladi are starting preparatory work to develop, and seek approvals for, a possible clinical trial to test telomere shortening and radiation treatment as a safer, more effective treatment for pediatric brain tumors.
Funding support for the current study in Cancer Prevention Research – published by the American Society for Cancer Research – came from the National Institutes of Health, the American Lebanese Syrian Associated Charities of St. Jude Children’s Research Hospital and Cincinnati Children’s Hospital Medical Center. Also collaborating were researchers from Children’s National Medical Center in Washington, D.C., and from St. Jude. Funding support for the Drissi lab’s correlative studies on the COG clinical trial comes from CancerFree Kids Pediatric Cancer Research Alliance and from Children’s Cancer Research Fund.
For more information about Cincinnati Children’s, please visit, http://www.cincinnatichildrens.org