MicroRNA-21 is overexpressed in pancreatic cancer and a potential predictor of survival.
MicroRNA-21 is overexpressed in pancreatic cancer and a potential predictor of survival.
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MicroRNA-21 在胰腺癌中过度表达,是生存的潜在预测因子。
DOI:
10.1007/s11605-008-0584-x
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发表时间:
2008-12
影响因子:
3.2
通讯作者:
Bloomston, Mark
中科院分区:
文献类型:
--
作者:
Dillhoff, Mary;Liu, James;Frankel, Wendy;Croce, Carlo;Bloomston, Mark
MicroRNAs are small (18–22 nucleotides) noncoding RNAs involved in posttranscriptional modification of many target genes. One of these, microRNA-21 (miR-21), has been shown to play a role in multiple hematologic and solid organ malignancies. We sought to determine the expression pattern of miR-21 in pancreatic cancers and its impact on clinicopathologic characteristics. Eighty resected pancreatic cancer specimens were microdissected and tissue microarrays (TMA) created in duplicate. TMAs were also created for benign pancreas (N=12) and chronic pancreatitis (N=45). In situ hybridization (ISH) was undertaken utilizing locked nucleic acid probes for miR-21. RNA U6 and scrambled RNA served as positive and negative control, respectively. ISH was scored as 0 (absent), 1+ (faint/focal expression), or 2+ (strong expression). Kaplan– Meier survival curves were constructed and compared by log-rank analysis. MiR-21 expression was demonstrated in 63 (79%) pancreatic cancers (1+ in 49, 2+ in 14) compared to one of 12 (8%, p<0.0001) benign pancreas and 12/45 (27%, p<0.0001) chronic pancreatitis. None of the benign tissues demonstrated strong miR-21 expression. Although miR-21 expression did not correlate with tumor size, differentiation, nodal status, or T stage, strong miR-21 expression was predictive of poorer outcome compared to absent or faint/focal miR-21 expression in patients with node-negative disease (median 27.7 months vs. 15.2, p=0.037). Nodal status was also predictive of survival (p=0.029). MicroRNA-21 is significantly overexpressed in pancreatic cancers as detected by in situ hybridization. Its strong expression predicts limited survival in patients with node-negative disease and may be an important biologic marker for outcome.
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影响因子:
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作者:
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通讯作者:
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影响因子:
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DOI:
10.1016/j.jtcvs.2007.08.055
发表时间:
2008-02-01
影响因子:
6
作者:
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通讯作者:
Litle, Virginia R.