Ovarian cancer is the deadliest of all cancers affecting the female reproductive system with very few effective treatments available. Prognosis is even worse among patients with certain subtypes of the disease. Researchers at The Wistar Institute have identified the target and the findings were published online by the journal Nature Medicine.
Ovarian cancer is divided into four different histological subtypes. One of the subtypes is ovarian clear cell carcinoma, which affects approximately 5 to 10 percent of American ovarian cancer patients and about 20 percent of patients in Asia. While most patients with ovarian cancer initially respond well to standard-care platinum-based chemotherapy, the response rate among those with the clear cell subtype is typically low and there is currently no effective therapy for these patients. This underscores the need for a new approach to treating this deadly disease.
The team at Wistar began by looking at ARID1A, a chromatin remodeler. When functioning normally, ARID1A makes it possible for chromatin - a cellular structure that holds DNA together in our cells - to open up and allow our cells to receive commands. This process dictates our cells' behavior and prevents them from becoming cancerous. However, recent studies have shown that ARID1A is mutated in more than 50 percent of cases of ovarian clear cell carcinoma. In fact, ARID1A has one of the highest mutation rates among all types of human cancer. To date, though, no therapies designed to target this common mutation have been described.
What interested the researchers was the relationship between ARID1A and EZH2, an enzyme that promotes compaction of the DNA. When this happens, the result is a loss of expression of genes in the compacted regions, thus preventing the transcription of DNA into tumor-fighting proteins for our body. While present in normal cells to maintain a transcriptional balance, an overabundance of EZH2 has been associated with the progression of different types of cancer, including ovarian clear cell carcinoma.
This prompted the team to explore the utility of EZH2 inhibition as a potential therapeutic means of treating cancer with ARID1A mutation. The interplay between ARID1A and EZH2 was confirmed when the researchers observed that ARID1A-mutated ovarian cancers are sensitive to EZH2 inhibition. Most exciting of all, EZH2 inhibition caused the regression of ovarian tumors with mutated ARID1A, while having minimal effects on the growth of ovarian tumor with normal or unmutated ARID1A in experimental models. Thus, the response to EZH2 inhibition correlates with ARID1A mutational status or the so-called "synthetic lethality."
"With EZH2 inhibitors currently in clinical development, we believe that our findings will have far-reaching implications," said Benjamin Bitler, Ph.D., a member of the Zhang laboratory, an American Cancer Society postdoctoral fellowship recipient, and first author of the study. "Excitingly, this study provides a much-needed therapeutic strategy for clear cell ovarian cancer and can be utilized to aid in the identification of patients that could benefit from EZH2 inhibition therapy."
"This study highlights the impact of how team science in our Cancer Center can bring about transformative discoveries," said Dario C. Altieri, M.D., director of The Wistar Institute Cancer Center and executive vice president and chief scientific officer of The Wistar Institute. "This has been our approach to better understand difficult-to-treat and recalcitrant tumors, like ovarian cancer, and we are thrilled that this groundbreaking research tangibly advances the prospects of better, more targeted therapies for these patients."
This work was supported by the National Institutes of Health grants R01CA160331 and R01CA16337, the U.S. Department of Defense Ovarian Cancer Academy Award OC093420 and the Ovarian Cancer Research Fund Program Project Development Grant. Other grants supporting this project include the American Cancer Society postdoctoral fellowship PF-13-058-01-TBA and the National Institutes of Health training grant T32CA9171-35. Core facilities support was provided by the Cancer Center Support Grant (CCSG) CA010815.
Other co-authors of this study from The Wistar Institute include Katherine M. Aird, Azat Garipov, Hua Li, Michael Amatangelo, Andrew V. Kossenkov, David C. Schultz, Qin Liu, José R. Conejo-Garcia, and David Speicher. Co-authors from other institutions included Ie-Ming Shih from Johns Hopkins Medical Institutions.
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