دورية أكاديمية

p21 promotes oncolytic adenoviral activity in ovarian cancer and is a potential biomarker

التفاصيل البيبلوغرافية
العنوان: p21 promotes oncolytic adenoviral activity in ovarian cancer and is a potential biomarker
المؤلفون: Lockley Michelle, Pirlo Katrina J, Salako Michael A, Archibald Kyra, Chelala Claude, Connell Claire M, Flak Magdalena B, Wheatley Sally P, Balkwill Frances R, McNeish Iain A
المصدر: Molecular Cancer, Vol 9, Iss 1, p 175 (2010)
بيانات النشر: BMC
سنة النشر: 2010
المجموعة: Directory of Open Access Journals: DOAJ Articles
مصطلحات موضوعية: Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
الوصف: The oncolytic adenovirus dl 922-947 replicates selectively within and lyses cells with a dysregulated Rb pathway, a finding seen in > 90% human cancers. dl 922-947 is more potent than wild type adenovirus and the E1B-deletion mutant dl 1520 (Onyx-015). We wished to determine which host cell factors influence cytotoxicity. SV40 large T-transformed MRC5-VA cells are 3-logs more sensitive to dl 922-947 than isogenic parental MRC5 cells, confirming that an abnormal G1/S checkpoint increases viral efficacy. The sensitivity of ovarian cancer cells to dl 922-947 varied widely: IC 50 values ranged from 51 (SKOV3ip1) to 0.03 pfu/cell (TOV21G). Cells sensitive to dl 922-947 had higher S phase populations and supported earlier E1A expression. Cytotoxicity correlated poorly with both infectivity and replication, but well with expression of p21 by microarray and western blot analyses. Matched p21+/+ and -/- Hct116 cells confirmed that p21 influences dl 922-947 activity in vitro and in vivo . siRNA-mediated p21 knockdown in sensitive TOV21G cells decreases E1A expression and viral cytotoxicity, whilst expression of p21 in resistant A2780CP cells increases virus activity in vitro and in intraperitoneal xenografts. These results highlight that host cell factors beyond simple infectivity can influence the efficacy of oncolytic adenoviruses. p21 expression may be an important biomarker of response in clinical trials.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 1476-4598
العلاقة: http://www.molecular-cancer.com/content/9/1/175Test; https://doaj.org/toc/1476-4598Test; https://doaj.org/article/13dfc844c9d54bfa95357eac97e4027fTest
DOI: 10.1186/1476-4598-9-175
الإتاحة: https://doi.org/10.1186/1476-4598-9-175Test
https://doaj.org/article/13dfc844c9d54bfa95357eac97e4027fTest
رقم الانضمام: edsbas.12A4D72B
قاعدة البيانات: BASE
الوصف
تدمد:14764598
DOI:10.1186/1476-4598-9-175