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PMID: 19092150 Published · ppublish English Comparative Study Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Dicer, Drosha, and outcomes in patients with ovarian cancer.

The New England journal of medicine ·Vol. 359 ·No. 25 ·2008-12-18 ·Pages 2641-50

Merritt WM, Lin YG, Han LY, Kamat AA, Spannuth WA, Schmandt R, Urbauer D, Pennacchio LA, Cheng JF, Nick AM, Deavers MT, Mourad-Zeidan A, Wang H, Mueller P, Lenburg ME, Gray JW, Mok S, Birrer MJ, Lopez-Berestein G, Coleman RL, Bar-Eli M, Sood AK

Abstract

We studied Dicer and Drosha, components of the RNA-interference machinery, in ovarian cancer. We measured messenger RNA (mRNA) levels of Dicer and Drosha in specimens of invasive epithelial ovarian cancer from 111 patients, using a quantitative reverse-transcriptase-polymerase-chain-reaction assay, and compared the results with clinical outcomes. Validation was performed with the use of published microarray data from cohorts of patients with ovarian, breast, and lung cancer. Mutational analyses of genomic DNA from the Dicer and Drosha genes were performed in a subgroup of ovarian-cancer specimens. Dicer-dependent functional assays were performed by means of in vitro transfection with small interfering RNA (siRNA) and short hairpin RNA (shRNA). Levels of Dicer and Drosha mRNA correlated with the levels of expression of the corresponding protein and were decreased in 60% and 51% of ovarian-cancer specimens, respectively. Low Dicer expression was significantly associated with advanced tumor stage (P=0.007), and low Drosha expression with suboptimal surgical cytoreduction (P=0.02). Cancer specimens with both high Dicer expression and high Drosha expression were associated with increased median survival (>11 years, vs. 2.66 years for other subgroups; P<0.001). We found three independent predictors of reduced disease-specific survival in multivariate analyses: low Dicer expression (hazard ratio, 2.10; P=0.02), high-grade histologic features (hazard ratio, 2.46; P=0.03), and poor response to chemotherapy (hazard ratio, 3.95; P<0.001). Poor clinical outcomes among patients with low Dicer expression were validated in additional cohorts of patients. Rare missense mutations were found in the Dicer and Drosha genes, but their presence or absence did not correlate with the level of expression. Functional assays indicated that gene silencing with shRNA, but not siRNA, may be impaired in cells with low Dicer expression. Our findings indicate that levels of Dicer and Drosha mRNA in ovarian-cancer cells have associations with outcomes in patients with ovarian cancer.

MeSH Terms
Adult Aged Aged, 80 and over Breast Neoplasms/genetics,metabolism Cell Line, Tumor DEAD-box RNA Helicases/genetics,metabolism DNA Mutational Analysis Endoribonucleases/genetics,metabolism Female Gene Expression Regulation, Neoplastic Humans Kaplan-Meier Estimate Lung Neoplasms/genetics,metabolism MicroRNAs/metabolism Middle Aged Multivariate Analysis Mutation, Missense Neoplasm Staging Neoplasms, Glandular and Epithelial/genetics,metabolism,mortality Ovarian Neoplasms/genetics,metabolism,mortality Prognosis RNA Interference RNA, Messenger/metabolism RNA, Small Interfering Reverse Transcriptase Polymerase Chain Reaction Ribonuclease III/genetics,metabolism Transfection Treatment Outcome
Chemicals
MicroRNAs RNA, Messenger RNA, Small Interfering Endoribonucleases DICER1 protein, human DROSHA protein, human Ribonuclease III DEAD-box RNA Helicases
Authors & Affiliations
22 authors, click to expand affiliations / ORCID
Merritt William M
University of Texas M.D. Anderson Cancer Center, Houston, TX 77230, USA.
Lin Yvonne G
Han Liz Y
Kamat Aparna A
Spannuth Whitney A
Schmandt Rosemarie
Urbauer Diana
Pennacchio Len A
Cheng Jan-Fang
Nick Alpa M
Deavers Michael T
Mourad-Zeidan Alexandra
Wang Hua
Mueller Peter
Lenburg Marc E
Gray Joe W
Mok Samuel
Birrer Michael J
Lopez-Berestein Gabriel
Coleman Robert L
Bar-Eli Menashe
Sood Anil K
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Article Info
Journal
The New England journal of medicine
Abbr.
N Engl J Med
ISSN
1533-4406
Published
2008-12-18
Pages
2641-50
Language
English
Region
United States
NLM ID
0255562
PMCID
PMC2710981
Subset
IM
Grants
NCI NIH HHS · R01 CA109298 · United States
NCI NIH HHS · R01 CA110793 · United States
NCI NIH HHS · CA110793 · United States
NCI NIH HHS · U54 CA112970 · United States
NCI NIH HHS · P50 CA083639 · United States
NCI NIH HHS · P50 CA083639-090008 · United States
NCI NIH HHS · T32 CA101642 · United States
NCI NIH HHS · CA109298 · United States
NCI NIH HHS · U54 CA112970-05 · United States
NCI NIH HHS · P50 CA58207 · United States
NCI NIH HHS · P50 CA058207 · United States
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