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The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.

Expression profiling identifies microRNA signature in pancreatic cancer

Open access
Lee, Eun Joo, Gusev, Yuriy, Jiang, Jinmai, Nuovo, Gerard J., Lerner, Megan R., Frankel, Wendy L., Morgan, Daniel L., Postier, Russell G., Brackett, Daniel J., Schmittgen, Thomas D.·2007·International Journal of Cancer

Abstract

microRNAs are functional, 22 nt, noncoding RNAs that negatively regulate gene expression. Disturbance of microRNA expression may play a role in the initiation and progression of certain diseases. A microRNA expression signature has been identified that is associated with pancreatic cancer. This has been accomplished with the application of real‐time PCR profiling of over 200 microRNA precursors on specimens of human pancreatic adenocarcinoma, paired benign tissue, normal pancreas, chronic pancreatitis and nine pancreatic cancer cell lines. Hierarchical clustering was able to distinguish tumor from normal pancreas, pancreatitis and cell lines. The PAM algorithm correctly classified 28 of 28 tumors, 6 of 6 normal pancreas and 11 of 15 adjacent benign tissues. One hundred microRNA precursors were aberrantly expressed in pancreatic cancer or desmoplasia (p < 0.01), including microRNAs previously reported as differentially expressed in other human cancers (miR‐155, miR‐21, miR‐221 and miR‐222) as well as those not previously reported in cancer (miR‐376a and miR‐301). Most of the top aberrantly expressed miRNAs displayed increased expression in the tumor. Expression of the active, mature microRNA was validated using a real‐time PCR assay to quantify the mature microRNA and Northern blotting. Reverse transcription in situ PCR showed that three of the top differentially expressed miRNAs (miR‐221, ‐376a and ‐301) were localized to tumor cells and not to stroma or normal acini or ducts. Aberrant microRNA expression may offer new clues to pancreatic tumorigenesis and may provide diagnostic biomarkers for pancreatic adenocarcinoma. © 2006 Wiley‐Liss, Inc.

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Metadata

Authors
Lee, E. J., Gusev, Y., Jiang, J., Nuovo, G. J., Lerner, M. R., Frankel, W. L., Morgan, D. L., Postier, R. G., Brackett, D. J., & Schmittgen, T. D.
Venue
International Journal of Cancer
Publisher
Wiley
Published
2006-12-05
Volume
120
Issue
5
Pages
1046-1054
ISSN
  • 0020-7136 (ISSN-L)
  • 1097-0215
OpenAlex
W2020080445
Cited by
896
References
7
FWCI
20.60
Type
journal article
Language
en
Open access
green

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