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| 1 | Predictive value of Ki67 and p53 in locally advanced rectal cancer:Correlation with thymidylate synthase and histopathological tumor regression after neoadjuvant 5-FU-based chemoradiotherapy显示文摘AIM: To investigate the predictive value of Ki67 and p53 and their correlation with thymidylate synthase (TS) gene expression in a rectal cancer patient cohort treated according to a standardized recommended neoadjuvant treatment regimen.METHODS: Formalin fixed, paraffin embedded pre-therapeutical tumor biopsies (n = 22) and post-therapeutical resection specimens (n = 40) from patients with rectal adenocarcinoma (clinical UICC stage Ⅱ/Ⅲ) receiving standardized neoadjuvant 5-fluorouracil (5-FU) based chemoradiotherapy were studied for Ki67 and p53 expression by immunohistochemistry and correlated with TS mRNA expression by quantitative TaqMan real-time PCR after laser microdissection. The results were compared with histopathological tumor regression according to a standardized semiquantitative score grading system.RESULTS: Responders (patients with high tumor regression) showed a significantly lower Ki67 expression than non-responders in the pre-therapeutical tumor biopsies (81.2% vs 16.7%; P < 0.05) as well as in the post-therapeutical resection specimens (75.8% vs 14.3%; P < 0.01). High TS mRNA expression was significantly correlated with a high Ki67 index and low TS mRNA expression was significantly correlated with a low Ki67 index in the pre-therapeutical tumor biopsies (corr. coef. = 0.46; P < 0.01) as well as in the post-therapeutical resection specimens (corr. coef. = 0.40; P < 0.05). No significant association was found between p53 and TS mRNA expression or tumor regression.CONCLUSION: Ki67 has, like TS, predictive value in rectal cancer patients after neoadjuvant 5-FU based chemoradiotherapy. The close correlation between Ki67 and TS indicates that TS is involved in active cell cycle processes. | Christiane Jakob Torsten Liersch Wolfdietrich Meyer Heinz Becker Gustavo B Baretton Daniela E Aust | 2008 | World Journal of Gastroenterology2008，14，7： | 29 |
| 2 | Serrated polyps of the colon and rectum (hyperplastic polyps, sessile serrated adenomas, traditional serrated adenomas, and mixed polyps)—proposal for diagnostic criteria显示文摘 | Daniela E. Aust Gustavo B. Baretton | 2010 | Virchows Archiv2010，，3： | 1 |
| 3 | Early esophageal cancer in Europe: endoscopic treatment by endoscopic submucosal dissection显示文摘 | Andreas Probst Daniela Aust Bruno M?rkl Matthias Anthuber Helmut Messmann | 2014 | Endoscopy2014，，： | 1 |
| 4 | Mutant p53 drives pancreatic cancer metastasis through cell-autonomous PDGF receptor beta signaling显示文摘 | Susann Weissmueller Eusebio Manchado Michael Saborowski John P. Morris Elvin Wagenblast Carrie A. Davis Sung-Hwan Moon Neil T. Pfister Darjus F. Tschaharganeh Thomas Kitzing Daniela Aust Elke K. Markert Jianmin Wu Sean M. Grimmond Christian Pilarsky Carol | 2014 | Cell2014，，： | 1 |
| 5 | Serrated polyps of the colon and rectum (hyperplastic polyps, sessile serrated adenomas, traditional serrated adenomas, and mixed polyps)—proposal for diagnostic criteria显示文摘 | Daniela E. Aust Gustavo B. Baretton | 2010 | Virchows Archiv2010，，3： | 1 |
| 6 | Pathohistological Subtype Predicts Survival in Patients With Intraductal Papillary Mucinous Neoplasm (IPMN) of the Pancreas显示文摘 | Marius Distler Stephan Kersting Marco Niedergethmann Daniela E. Aust Melanie Franz Felix Rückert Florian Ehehalt Christian Pilarsky Stefan Post Hans-Detlev Saeger Robert Grützmann | 2013 | Annals of Surgery2013，，2： | 1 |
| 7 | Pathohistological Subtype Predicts Survival in Patients With Intraductal Papillary Mucinous Neoplasm (IPMN) of the Pancreas显示文摘 | Marius Distler Stephan Kersting Marco Niedergethmann Daniela E. Aust Melanie Franz Felix Rückert Florian Ehehalt Christian Pilarsky Stefan Post Hans-Detlev Saeger Robert Grützmann | 2013 | Annals of Surgery2013，，2： | 1 |
| 8 | Histology of microscopic colitis—review with a practical approach for pathologists显示文摘 | Cord Langner Daniela Aust Arzu Ensari Vincenzo Villanacci Gabriel Becheanu Stephan Miehlke Karel Geboes Andreas Münch | 2015 | Histopathology2015，，5： | 1 |
| 9 | Value of histomorphometric tumour thickness and smoothelin for conventional m-classification in early oesophageal adenocarcinoma显示文摘AIM To test the validity of tumour thickness measurement in distinguishing between the different infiltration depths, especially when the duplication of muscularis mucosae cannot be demarcated clearly. METHODS We re-evaluated 100 completely embedded Barrett's adenocarcinomas regarding m-classification, maximum tumour thickness, and muscularis mucosae duplication. For validation, smoothelin staining was performed on a subset of cases. RESULTS The m1-, m2-and m3-classified adenocarcinomasshowed a significant lower tumour thickness compared to the m4-and sm1-classified lesions(P < 0.001). Smoothelin staining determined a clear muscularis mucosae duplication in 64% of the tested samples and enabled the differentiation of the two layers in diffuse and merged splits. CONCLUSION Tumour thickness in early oesophageal adenocarcinoma significantly correlates with the depth of infiltration and demonstrates its worth as an accurate p T classification in non-polypoid lesions. We created a new algorithm, which combines histomorphology with morphometric analyses. It is noteworthy that it facilitates the assessment of mucosal vs submucosal infiltration depth. The smoothelin staining strengthened our results of the tumour thickness evaluation and can be used in cases of doubt. | Katharina Endhardt Bruno Markl Andreas Probst Tina Schaller Daniela Aust | 2017 | World Journal of Gastrointestinal Oncology2017，9，11： | 0 |
| 10 | Expression profiling of gastric cancer samples by oligonucleotide microarray analysis reveals low degree of intra-tumor variability显示文摘AIM: Gene expression profiling provides an unique opportunity to gain insight into the development of different types of gastric cancer. Tumor sample heterogeneity is thought to decrease the sensitivity and tumor specificity of microarray analysis. Thus, microdissection and preamplification of RNA is frequently performed. However, this technique may also induce considerable changes to the expression profile. To assess the effect of gastric tumor heterogeneity on expression profiling results, we measured the variation in gene expression within the same gastric cancer sample by performing a gene chip analysis with two RNA preparations extracted from the same tumor specimen.METHODS: Tumor samples from six intestinal T2 gastric tumors were dissected under liquid nitrogen and RNA was prepared from two separate tumor fragments. Each extraction was individually processed and hybridized to an Affymetrix U133A gene chip covering approximately 18 000 human gene transcripts. Expression profiles were analyzed using Microarray Suite 5.0 (Affymetrix) and GeneSpring 6.0 (Silicon Genetics).RESULTS: All gastric cancers showed little variance in expression profiles between different regions of the same tumor sample. In this case, gene chips displayed mean pair wise correlation coefficients of 0.94±0.02 (mean±SD),compared to values of 0.61±0.1 for different tumor samples. Expression of the variance between the two expression profiles as a percentage of 'total change'(Affymetrix) revealed a remarkably low average value of 1.18±0.78 for comparing fragments of the same tumor sample.In contrast, comparison of fragments from different tumors revealed a percentage of 24.4±4.5.CONCLUSION: Our study indicates a low degree of expression profile variability within gastric tumor samples isolated from one patient. These data suggest that tumor tissue heterogeneity is not a dominant source of error for microarray analysis of larger tumor samples, making total RNA extraction an appropriate strategy for performing gene chip expression profiling of gastric cancer. | Karolin Trautmann Christine Steudel Dana Grossmann Daniela Aust Gerhard Ehninger Stephan Miehike Christian Thiede | 2005 | World Journal of Gastroenterology2005，11，38： | 0 |
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