000130302 001__ 130302 000130302 005__ 20240228143423.0 000130302 0247_ $$2doi$$a10.3390/ijms17101755 000130302 0247_ $$2pmid$$apmid:27775664 000130302 0247_ $$2pmc$$apmc:PMC5085780 000130302 0247_ $$2ISSN$$a1422-0067 000130302 0247_ $$2ISSN$$a1661-6596 000130302 0247_ $$2altmetric$$aaltmetric:12981880 000130302 037__ $$aDKFZ-2017-05381 000130302 041__ $$aeng 000130302 082__ $$a570 000130302 1001_ $$aPecqueux, Mathieu$$b0 000130302 245__ $$aA Comprehensive MicroRNA Expression Profile of Liver and Lung Metastases of Colorectal Cancer with Their Corresponding Host Tissue and Its Prognostic Impact on Survival. 000130302 260__ $$aBasel$$bMolecular Diversity Preservation International$$c2016 000130302 3367_ $$2DRIVER$$aarticle 000130302 3367_ $$2DataCite$$aOutput Types/Journal article 000130302 3367_ $$0PUB:(DE-HGF)16$$2PUB:(DE-HGF)$$aJournal Article$$bjournal$$mjournal$$s1522223404_30780 000130302 3367_ $$2BibTeX$$aARTICLE 000130302 3367_ $$2ORCID$$aJOURNAL_ARTICLE 000130302 3367_ $$00$$2EndNote$$aJournal Article 000130302 520__ $$aMicroRNAs are small non-coding RNAs with a length of 18-25 nucleotides. They can regulate tumor invasion and metastasis by changing the expression and translation of their target mRNAs. Their expression is substantially altered in colorectal cancer cells as well as in the adjacent tumor-associated stroma. Both of these compartments have a mutual influence on tumor progression. In the development of metastases, cancer cells initially interact with the host tissue. Therefore, compartment-specific expression signatures of these three locations-tumor, associated stroma, and host tissue-can provide new insights into the complex tumor biology of colorectal cancer. Frozen tissue samples of colorectal liver (n = 25) and lung metastases (n = 24) were laser microdissected to separate tumor cells and the adjacent tumor-associated stroma cells. Additionally, normal lung and liver tissue was collected from the same patients. We performed a microarray analysis in four randomly selected liver metastases and four randomly selected lung metastases, analyzing a total of 939 human miRNAs. miRNAs with a significant change >2-fold between the tumor, tumor stroma, and host tissue were analyzed in all samples using RT-qPCR (11 miRNAs) and correlated with the clinical data. We found a differential expression of several miRNAs between the tumor, the tumor-associated stroma, and the host tissue compartment. When comparing liver and lung metastases, miR-194 showed a 1.5-fold; miR-125, miR-127, and miR-192 showed a 2.5-fold; miR-19 and miR-215 a 3-fold; miR-145, miR-199-3, and miR-429 a 5-fold; miR-21 a 7-fold; and, finally, miR-199-5 a 12.5-fold downregulation in liver metastases compared to lung metastases. Furthermore miR-19, miR-125, miR-127, miR-192, miR-194, miR-199-5, and miR-215 showed a significant upregulation in the normal liver tissue compared to the normal lung tissue. Univariate analysis identified an association of poor survival with the expression of miR-125 (p = 0.05), miR-127 (p = 0.001), miR-145 (p = 0.005), miR-192 (p = 0.015), miR-194 (0.003), miR-199-5 (p = 0.008), miR-215 (p < 0.001), and miR-429 (p = 0.03) in the host liver tissue of the liver metastases. Colorectal liver and lung metastases have a unique miRNA expression profile. miRNA expression in the host tissue of colorectal liver metastases seems to be able to influence tumor progression and survival. These findings can be used in the development of tailored therapies. 000130302 536__ $$0G:(DE-HGF)POF3-313$$a313 - Cancer risk factors and prevention (POF3-313)$$cPOF3-313$$fPOF III$$x0 000130302 588__ $$aDataset connected to CrossRef, PubMed, 000130302 650_7 $$2NLM Chemicals$$aMicroRNAs 000130302 7001_ $$aLiebetrau, Isabell$$b1 000130302 7001_ $$0P:(DE-HGF)0$$aWerft, Wiebke$$b2 000130302 7001_ $$aDienemann, Hendrik$$b3 000130302 7001_ $$aMuley, Thomas$$b4 000130302 7001_ $$aPfannschmidt, Joachim$$b5 000130302 7001_ $$aMüssle, Benjamin$$b6 000130302 7001_ $$aRahbari, Nuh$$b7 000130302 7001_ $$aSchölch, Sebastian$$b8 000130302 7001_ $$aBüchler, Markus W$$b9 000130302 7001_ $$aWeitz, Jürgen$$b10 000130302 7001_ $$aReissfelder, Christoph$$b11 000130302 7001_ $$aKahlert, Christoph$$b12 000130302 773__ $$0PERI:(DE-600)2019364-6$$a10.3390/ijms17101755$$gVol. 17, no. 10, p. 1755 -$$n10$$p1755 -$$tInternational journal of molecular sciences$$v17$$x1422-0067$$y2016 000130302 909CO $$ooai:inrepo02.dkfz.de:130302$$pVDB 000130302 9101_ $$0I:(DE-588b)2036810-0$$6P:(DE-HGF)0$$aDeutsches Krebsforschungszentrum$$b2$$kDKFZ 000130302 9131_ $$0G:(DE-HGF)POF3-313$$1G:(DE-HGF)POF3-310$$2G:(DE-HGF)POF3-300$$3G:(DE-HGF)POF3$$4G:(DE-HGF)POF$$aDE-HGF$$bGesundheit$$lKrebsforschung$$vCancer risk factors and prevention$$x0 000130302 9141_ $$y2016 000130302 915__ $$0StatID:(DE-HGF)0100$$2StatID$$aJCR$$bINT J MOL SCI : 2015 000130302 915__ $$0StatID:(DE-HGF)0200$$2StatID$$aDBCoverage$$bSCOPUS 000130302 915__ $$0StatID:(DE-HGF)0300$$2StatID$$aDBCoverage$$bMedline 000130302 915__ $$0StatID:(DE-HGF)0310$$2StatID$$aDBCoverage$$bNCBI Molecular Biology Database 000130302 915__ $$0StatID:(DE-HGF)0501$$2StatID$$aDBCoverage$$bDOAJ Seal 000130302 915__ $$0StatID:(DE-HGF)0500$$2StatID$$aDBCoverage$$bDOAJ 000130302 915__ $$0LIC:(DE-HGF)CCBYNV$$2V:(DE-HGF)$$aCreative Commons Attribution CC BY (No Version)$$bDOAJ 000130302 915__ $$0StatID:(DE-HGF)0600$$2StatID$$aDBCoverage$$bEbsco Academic Search 000130302 915__ $$0StatID:(DE-HGF)0030$$2StatID$$aPeer Review$$bASC 000130302 915__ $$0StatID:(DE-HGF)0199$$2StatID$$aDBCoverage$$bThomson Reuters Master Journal List 000130302 915__ $$0StatID:(DE-HGF)0111$$2StatID$$aWoS$$bScience Citation Index Expanded 000130302 915__ $$0StatID:(DE-HGF)0150$$2StatID$$aDBCoverage$$bWeb of Science Core Collection 000130302 915__ $$0StatID:(DE-HGF)1150$$2StatID$$aDBCoverage$$bCurrent Contents - Physical, Chemical and Earth Sciences 000130302 915__ $$0StatID:(DE-HGF)9900$$2StatID$$aIF < 5 000130302 9201_ $$0I:(DE-He78)C060-20160331$$kC060$$lBiostatistik$$x0 000130302 980__ $$ajournal 000130302 980__ $$aVDB 000130302 980__ $$aI:(DE-He78)C060-20160331 000130302 980__ $$aUNRESTRICTED